Akhil A.
Bhosle
,
Mainak
Banerjee
* and
Amrita
Chatterjee
*
Department of Chemistry, BITS-Pilani, K K Birla Goa Campus, NH 17B Bypass Road, Zuarinagar 403726, Goa, India. E-mail: p20190018@goa.bits-pilani.ac.in; mainak@goa.bits-pilani.ac.in; amrita@goa.bits-pilani.ac.in; Tel: +91 832 2580 347 Tel: +91 832 2580 320
First published on 11th April 2024
Azines are an important class of compounds that display solvent-dependent fluorescence emission depending upon the substituents in the aromatic scaffolds. They are affordable, easy to synthesize, stable, and well-suited for numerous applications. Unlike most other AIE fluorophores, aromatic units of AIE-active azine derivatives are bridged by rotatable N–N bonds rather than C–C bonds. Their derivatives have been widely used in pharmaceuticals, drug delivery, organometallics, optoelectronics, dyes, etc., and most importantly in several sensing applications. This comprehensive review encapsulates the recent developments in the field of AIE-active azine molecules and their applications as chemosensors in the detection of various analytes. The review discusses the different chemosensing strategies involved in the detection of metal ions (Cu2+, Zn2+, Al3+, Fe3+, Cr3+, Hg2+, UO22+, etc.), anions (F−, CN−, ClO−, ONOO−, HSO3−), small molecules (thiols, hydrazine, hydrogen peroxide), and bio-analytes (protamine/heparin, HSA/BSA, neuraminidase, β-lactamase, β-galactosidase, etc.) with a focus on the development in the last five years. The review also highlights the advancements in azine-based systems for their use in imaging, supramolecular host–guest recognitions, AIE polymers, COFs/MOFs, etc.
Conventional fluorophores exhibit strong fluorescence emissions in diluted organic solvents. However, a partial or complete quenching is displayed upon aggregation or in concentrated solutions, reducing their overall efficiency in sensing and bioimaging of the analytes.5 This effect is called the concentration quenching or the aggregation-caused quenching (ACQ) effect. One of the primary examples of the ACQ effect was studied by Förster and Kasper in 1955, wherein they observed a decrease in the fluorescence emission of pyrene upon increasing the concentration due to the formation of sandwich-shaped excimers and exciplexes (disc-like structures) at the excited state.6 However, Prof. B. Z. Tang introduced the exact reverse phenomenon in 2001 for a new set of luminophores that fluoresce strongly upon aggregation and could overcome the disadvantages of the ACQ molecules. They coined the term “aggregation-induced emission” to explain the strong emission of propeller-shaped non-planar molecule 1,1′,2,3,4,5-hexaphenyl-1H-silole (HPS) by increasing the water fractions in a THF solution.7 Subsequently, several molecules exhibiting AIE phenomena have been reported in the last two decades and are termed “AIEgens”.8 AIEgens display multiple advantages compared to traditional ACQ molecules in their high fluorescence quantum yield in aggregated states and at higher concentrations, significant Stokes shift, and low cytotoxicity.
AIE-active azine molecules have paved the way for innovative technologies in diverse areas including chemosensing,3 organic electronic devices,9 nanomaterials,10 electro-optical devices,11 organic functional materials,12 battery materials,13 COFs,14 imaging studies,15,16 drug delivery,17 supramolecular chemistry,18 light-harvesting systems,19etc. Over the years, there have been many milestone developments in the field of AIE-active azine-based chemosensors (Scheme 1). As a first report, Tong and co-workers reported the synthesis of a range of salicylaldehyde azines which exhibited noteworthy AIE properties depending on the substitutions on the aromatic scaffold.20 In 2010, Chen et al. developed a carboxylic acid functionalized azine derivative that carries a negative charge in basic pH and demonstrated it for the detection of positively charged protamine owing to their electrostatic interactions.21 In 2014, an azine-derived flavone-based ratiometric probe was reported by Peng et al. for the detection of Al3+ ions in the solution phase which was one of the early developments in azines as chemosensors for metal ions.22 Subsequently, Xu et al. reported an amphiphilic AIE-active azine, a cationic bola-amphiphile with a salicylaldehyde azine moiety that undergoes a 30-fold emission enhancement upon the addition of γ-cyclodextrin due to the formation of a [2]pseudorotaxane inclusion complex.18 The azine probe can specifically localize in mitochondria of living cells for fluorescent imaging. In 2016, Liu and co-workers demonstrated an azine-linked luminescent 2D-covalent organic framework incorporating salicylaldehyde with bulky groups as building blocks, which was utilized for Cu2+ ion sensing in a selective and sensitive manner.23 The development of an unsymmetrical azine-derived probe with a naphthalimide moiety was reported by Kumar and co-workers which was utilized for the ratiometric detection of Al3+ ions in the solution phase.24 At a similar time, Zhang & co-workers developed an AIE-active azine-based chemodosimeter by tert-butyl dimethylsilyl protection for the sensing of fluoride ions.25 In 2018, Tang & co-workers reported a tetraphenylethylene-conjugated AIE-active azine by condensation of two TPE units that could recognize Cu2+ ions.26 A year later, Nguyen et al. synthesized a water-soluble azine probe to detect Al3+ in aqueous solutions.27 In 2020, Manigandan et al. reported a salicylaldehyde-based double azine probe as a highly reliable Fe3+ sensor.28 In the next year, an azine with ESIPT-TICT-AIE triple photophysical characteristics, which is fluorescent both in solution and solid phase featuring orange emission, was reported by our group for the first time and demonstrated in the turn-off sensing of Cu2+ ions both in solution and solid phase.29 Our group further envisaged an AIE active NIR-emissive unsymmetrical azine as a dual-mode-dual-chemodosimeter for the selective and sensitive detection of toxic analytes, N2H4 and HSO3−.30 The upcoming section will reflect the advancements in the realm of AIE-active luminogens based on the azine moiety, shedding light on their design, synthesis, optical properties and diverse chemosensing applications. Furthermore, the use of azines in supramolecular sensing, and various azine-derived materials like polymers, MOFs, and COFs in chemosensing applications has been captured in this review. Azines as dual sensors in multi-targeted sensing and imaging are also covered.
In one of the early attempts, Tong and co-workers synthesized a series of salicylaldehyde-based azine compounds (1) that showed appreciable aggregation-induced emission properties [Fig. 1A].20 These compounds fluoresced weakly in good organic solvents but strongly in poor solvents. Depending on the substituents in the aromatic scaffold, these azines displayed green to orange emission (λmax = 513 nm to 570 nm). The unsubstituted azine, 1b, displayed yellow emission at λmax 542 nm, whereas when the electron-donating OH group is at the 4-position, azine 1a showed intense emission at λmax 513 nm. Notably, with the presence of a –Cl substituent at the 5-position, the emission of 1c showed a red shift to λmax 570 nm. These azines were further explored in hydrazine sensing, which will be discussed later. The same group further envisaged that a planar conjugated core attached to a donor–acceptor (D–A) pair might be a design principle for developing new organic materials with solid luminescence-switching properties. Accordingly, they investigated a symmetrical azine, 2, for its solid-state fluorescence properties by incorporating a strong electron-donating diethylamino group at the 4-position of the salicylaldehyde azine [Fig. 1B].31 The azine was responsive to external stimuli like mechanical grinding and temperature. The yellow fluorescence of the compound with emission at 550 nm underwent a significant hypsochromic shift upon grinding or annealing to generate another crystalline form of 2 which emits at 529 nm. The solid-phase transformation with reduced π–π interactions also afforded an amorphous solid that emits at 529 nm with a shoulder peak at 550 nm with intense green fluorescence. The presence of the donor diethylamino group and the acceptor azine moiety functions as a push–pull system and is crucial for solid-state fluorescence-switching. The azines with such push–pull groups could potentially be used in new pressure/thermo-sensing devices. In their continuous study, the authors further synthesized a conformationally flexible symmetrical azine, 3, by condensing hydrazine with (2-hydroxy-4-methoxyphenyl)(phenyl)-methanone [Fig. 1C].32 They studied its ESIPT fluorescence changes with respect to the two different polymorphs, green and yellowish green fluorescence, respectively. It was observed that the green emitting polymorph, when annealed at 231 °C for 1 h, induced the phenyl units to stray from their energetically preferred vertical conformation by stronger interactions between them. In contrast, annealing the yellowish-green polymorph eliminated intermolecular connection, restoring the energetically favored conformation. Thus, by alternating annealing/melting procedures, the azine ESIPT fluorescence could be reversibly modified with different emission wavelengths having substantial Stokes shift, high stability and quantum yield.
Fig. 1 Selected examples of AIE-active azine compounds studied for their photophysical properties (adapted with permission from: (A) ref. 20. Copyright 2009, American Chemical Society; (B) ref. 31. Copyright 2011, American Chemical Society; (C) ref. 32. Copyright 2013, American Chemical Society; (D) ref. 33. Copyright 2015, Wiley-VCH; (E) ref. 34. Copyright 2017, Royal Society of Chemistry; (F) ref. 35. Copyright 2020, Royal Society of Chemistry; (G) ref. 36. Copyright 2022, Elsevier). |
Yao et al. could inculcate mechanochromism in a commercial dye, Pigment Yellow 101. The dye, 4, was susceptible to mechanical grinding or heat and switched between two structurally distinct polymorphs [Fig. 1D].33 It was observed that the yellow fluorescence at 543 nm from one polymorph gets converted to the second polymorph with green emission at 530 nm upon grinding in a mortar pestle. In contrast, adding THF or 1,4-dioxane and further grinding after removal of the solvent results in a piezofluorochromic behavior to afford the third polymorph with emission at 566 nm. When heated to 285 °C and annealed, the polymorph converts from yellow to green fluorescence. A reversible transition was obtained after melting and cooling quickly to afford the two original polymorphs.
Samanta et al. demonstrated unsymmetrical azines, 5, to emit white light from a single-component system [Fig. 1E].34 The naphthol moiety and the azine linkage induced AIE behavior in these compounds and the emission of the azine could be tuned with different water percentages in methanol–water and acetonitrile–water combinations. The introduction of a phenyl (5a), naphthyl (5b) and pyrene (5c) moiety was investigated for linking the AIE scaffold of the naphthyl moiety with dual emission behavior (comprising complementary emission colors) to obtain white light. It was observed that compounds 5a and 5b fluoresced strongly at 510 nm and 521 nm, respectively. However, the presence of the pyrene moiety in 5c afforded a distinct extra emission peak owing to its tendency to form an excimer and resulted in two peaks at 472 and 560 nm. 5c exhibited variable emission based on the change in the percentage of water and emitted white fluorescence at 70%, 80% and 90% water fractions.
Mathivanan et al. synthesized a short series of donor–acceptor unsymmetrical azines, 6, by condensation of triphenylamine hydrazone and various salicylaldehyde derivatives [Fig. 1F].35 The azines were designed by utilizing electron-rich triphenylamine as the donor and AIE-active core that also introduces ICT behavior in the scaffold. The imine nitrogen of the azine linkage acts as an electron acceptor and the incorporation of salicylaldehyde units further induces ESIPT behavior with tunable characteristics in the system. The crystal structures confirmed the formation of a supramolecular network from the weak solid-state interactions in addition to the solvent polarity-dependent positive solvatochromic behavior. Electron-donating triphenylamine and diethylamino groups on the scaffold induced pH-dependent emissive properties in the solution. In a continuous effort, the same group further reported a short series of triphenylamine-based symmetrical azines (7) involving an acceptor–donor–acceptor type moiety [Fig. 1G].36 In an attempt to incorporate the ESIPT property in the acceptor–donor–acceptor symmetrical systems, similar to the previous report, an electron-rich triphenylamine unit was utilized as the AIE core as well as the strong donor unit, whereas substituted salicylaldimine units were utilized as electron acceptor groups along with the ESIPT unit. The azines showed weak fluorescence in solution and significant multi-color emission in the aggregated/solid state, depending on the peripheral substituent owing to the ESIPT and AIE properties. The presence of the methoxy group on the aromatic scaffold was found to exhibit a bathochromic shift and ultimately afford red emission.
Recently, our group discussed the design principle for unsymmetrical azines displaying ESIPT-TICT-AIE triple photophysical properties by combining hydroxybenzothiazole and benzophenone hydrazones [Fig. 2A].37 The incorporation of a hydroxybenzothiazole (HBT) unit rendered the ESIPT property in the system by keto–enol tautomerism, whereas the azine linkage along with the two phenyl units of hydrazone induces TICT property in the scaffold. The greener and cost-effective mechanochemical method afforded the azine compounds within a short time, avoiding harmful solvents and tedious workup procedures. The orange-to-red emissive azines are highly fluorescent and displayed ESIPT characteristics in organic solvents and AIE characteristics with increased water fractions [Fig. 2A]. The azines revealed solvent-polarity-dependent emission intensities and wavelength shifts based on luminophore aggregation with the maximum emission at 90–93% water fractions in most cases. Incorporating an electron-donating group at the diphenyl methylene unit facilitates electron donation from the donor to the acceptor unit, and a noticeable red shift is observed with the highest red-emission up to 680 nm (8a–d). Similarly, the presence of an EWG at the donor moiety lowered the emission wavelength (8b). The azines exhibited high quantum yields in different solvents and showed high fluorescence emission in the solid state as well. The molecules displayed a D1–A–D2 (or D–π–A) character due to the presence of an EDG (or EWG) at the HBT unit and electron shift from the electron-rich donor diphenyl methylene unit to the acceptor benzothiazole moiety along the azine linkage.
Fig. 2 (A) HBT-based unsymmetrical azine dyes (8) having ESIPT-TICT-AIE triple photophysical characteristics (adapted with permission from: ref. 37. Copyright 2023, Wiley-VCH); (B) change in the response of 9 towards LiOH, NaOH, and KOH and their possible molecular arrangement; (C) multi-stimuli responses shown by the metallogel under UV irradiation, ultrasound, mechanical stress and temperature change (images B and C are adapted with permission from ref. 38. Copyright 2018, Royal Society of Chemistry). |
In another study, Dixit et al. synthesized a fluorescent metallogel (1% w/v) from a symmetrical azine (9) with LiOH in a CHCl3–MeOH mixture [Fig. 2B].38 The chelation of Li+ with 9 leads to the inhibition of excited state intramolecular proton transfer (ESIPT) or the origin of fluorescence through chelation-enhanced fluorescence (CHEF), and gelation from aggregation. The metallogel exhibited multi-stimuli responses towards thermal and mechanical stress as well as reswelling properties [Fig. 2C].
Sr. no. | Probe | Analyte | Mechanism/strategy | λ ab | Solvent system | LOD | Remark | Ref. |
---|---|---|---|---|---|---|---|---|
λ em | ||||||||
(Δλ) | ||||||||
1 | 10a, R = H | Cu2+ | Turn-off/complexation (10:Cu2+ = 1:1) | 10a: 400 nm | Phosphate buffer–ACN (9:1 v/v, 10 mM, pH 7.4) | 10a: 0.15 μM | Fluorescence retrieval with S2− | 46 |
552 nm | ||||||||
(152 nm) | ||||||||
10b, R = Cl | 10b: 400 nm | 10b: 0.1 μM | ||||||
Zhou et al. (2018) | 536 nm | |||||||
(136 nm) | ||||||||
2 | 8a, Bhosle et al. (2021) | Cu2+ | Turn-off/complexation (8a:Cu2+ = 2:1) | 373 nm | H2O–DMF (9:1 v/v) | 0.005 μM | Fluorescence retrieval with AA | 29 |
590 nm | ||||||||
(217 nm) | ||||||||
3 | 11, Tharmalingam et al. (2019) | Cu2+ | Turn-off/complexation (11:Cu2+ = 1:3) | 430 nm | ACN–Tris·HCl buffer (9:1 v/v, 10 mM, pH 7.2) | 0.23 μM | Fluorescence retrieval with S2− | 47 |
470 nm | ||||||||
(40 nm) | Application in solid-phase detection | |||||||
4 | 12, Zhao et al. (2018) | Cu2+ | Turn-off/complexation (12:Cu2+ = 2:1) | 380 nm | H2O–THF (9:1 v/v) | 0.03 μM | Fluorescence retrieval with cysteine | 26 |
581 nm | ||||||||
(201 nm) | ||||||||
5 | 13, Tiwari et al. (2018) | Cu2+ | Turn-off/complexation (13:Cu2+ = 1:1) | 406 nm | EtOH–HEPES buffer (1:1 v/v, 10 mM, pH = 7.4) | 0.34 μM | Fluorescence retrieval with PO43−, HPO42−, H2PO4− | 48 |
537 nm | ||||||||
(131 nm) | ||||||||
6 | 14, Ye et al. (2021) | Cu2+ | Turn-off/complexation (14:Cu2+ = 1:1) | 400 nm | THF–HEPES buffer (1:19 v/v, 20 mM, pH 7.4) | 0.16 μM | Fluorescence retrieval with S2− | 49 |
515 nm | ||||||||
(115 nm) | ||||||||
7 | 10a, Liu et al. (2022) | Cu2+ | Turn-off/complexation (10a:Cu2+ = 1:2) | 350 nm | H2O–ACN (9:1 v/v) | 0.57 μM | — | 50 |
544 nm | ||||||||
(194 nm) | ||||||||
8 | 15a, R = H | Cu2+ | Turn-on/complexation (15:Cu2+ = 1:1) | 350 nm | CAN | 15a: 0.0008 μM | Fluorescence turn-on response toward CN− | 51 |
15b, R = Me | 510 nm | 15b: 0.0013 μM | ||||||
15c, R = F | (160 nm) | 15c: 0.0013 μM | ||||||
Kumarasamy et al. (2022) | ||||||||
9 | 16, Sharifi et al. (2023) | Cu2+ | Turn-on/complexation (16:Cu2+ = 1:1) | 335 nm | H2O–ACN (1:4 v/v) | 4.2 μM | — | 52 |
671 nm | ||||||||
(336 nm) | ||||||||
10 | 17, Kumar et al. (2018) | Al3+ | Turn-on/complexation (17:Al3+ = 1:1) | 335 nm | MeOH | 0.27 μM | Application in solid-phase detection | 53 |
490 nm | ||||||||
(155 nm) | ||||||||
11 | 18, Nguyen et al. (2019) | Al3+ | Turn-on/complexation (18:Al3+ = 1:1) | 390 nm | HEPES buffer (10 mM, pH 7) | 0.153 μM | Application in microfluidic detection | 27 |
511 nm | ||||||||
(121 nm) | ||||||||
12 | 19, Khanra et al. (2020) | Al3+ | Turn-on/complexation (19:Al3+ = 1:1) | 326 nm | SDS media (0.1 M HEPES, pH 7.4) | 0.0628 μM | — | 54 |
400 nm | ||||||||
(74 nm) | ||||||||
13 | 20, Khanra et al. (2019) | Zn2+ | Turn-on/complexation (20:Zn2+ = 1:1) | 400 nm | DMSO–bis-Tris buffer (1:1 v/v, pH 7.4) | 0.0335 μM | — | 55 |
495 nm | ||||||||
(95 nm) | ||||||||
14 | 21, Das et al. (2021) | Zn2+ | Turn-on/complexation (21:Zn2+ = 1:2) | 410 nm | DMSO–HEPES buffer (9:1 v/v, pH 7.2) | 2.18 μM | Fluorescence quenching with picric acid | 56 |
532 nm | ||||||||
(122 nm) | Application in logic gates | |||||||
15 | 22, Musikavanhu et al. (2022) | Cr3+ | Turn-off/complexation (22:Cr3+ = 1:1) | 408 nm | 0.2 M HEPES buffer, pH 7.2 | 0.041 μM | Application in solid-phase detection | 57 |
526 nm | ||||||||
(118 nm) | ||||||||
16 | 23, Manigandan et al. (2020) | Fe3+ | Turn-off/complexation (23:Fe3+ = 1:1) | 377 nm | H2O–DMF (1:1 v/v) | 0.077 μM | Fluorescence retrieval with EDTA | 28 |
423 nm | ||||||||
(46 nm) | ||||||||
17 | 24, Mondal et al. (2020) | Hg2+ | Turn-on/complexation (24:Hg2+ = 1:1) | 360 nm | H2O–EtOH (1:9 v/v) | 0.22 μM | Fluorescence turn-off response towards picric acid | 58 |
447 nm | ||||||||
(87 nm) | ||||||||
18 | 25, Tong et al. (2020) | Hg2+ | Turn-on/complexation | 417 nm | H2O–THF (4:1 v/v) | 7.07 μM | Fluorescence turn-off response towards Cu2+ | 59 |
558 nm | ||||||||
(141 nm) | ||||||||
19 | 26, Ghosh et al. (2018) | Mo6+ | Ratiometric/complexation (26:Mo6+ = 1:2) | 342 nm | EtOAc–HEPES buffer (10:1 v/v, 10 mM, pH 7.4) | 0.002 μM | Fluorescence retrieval with S2− | 60 |
501 nm ↑ and 415 nm ↓ | ||||||||
(73 nm) | ||||||||
20 | 27, Pham et al. (2019) | UO22+ | Turn-off/complexation (27:UO22+ = 1:1) | 365 nm | H2O–ACN (3:2 v/v) | 0.023 μM | — | 61 |
550 nm | ||||||||
(185 nm) | ||||||||
21 | 28, Yadav et al. (2019) | Al3+ and Cu2+ | Al3+: turn-on, Cu2+: turn-off/complexation (28:Al3+/Cu2+ = 1:1) | 434 nm | DMSO–HEPES–MeOH (0.1:1.9:8.0 v/v, pH 7.4) | Al3+: 0.16 μM | Fluorescence quenching with F− and retrieval with EDTA | 62 |
534 nm | ||||||||
(100 nm) | ||||||||
Cu2+: 0.15 μM | Application in solid-phase detection | |||||||
22 | 29, Sun et al. (2023) | Al3+ and Cu2+ | Turn-off/complexation (29:Al3+/Cu2+ = 1:1) | 365 nm | Al3+: H2O–DMSO (1:4 v/v) | Al3+: 8.47 μM | Application in solid-phase detection | 63 |
530 nm | ||||||||
(165 nm) | ||||||||
Cu2+: H2O–DMSO (7:3 v/v) | Cu2+: 0.17 μM | |||||||
23 | 30, Das et al. (2021) | Al3+ and Zn2+ | Turn-on/complexation (30:Al3+/Zn2+ = 1:1) | 405 nm | MeOH–HEPES buffer (9:1 v/v, pH 7.2) | Al3+: 9.78 μM | Application in logic gates | 64 |
532 nm | ||||||||
(127 nm) | Zn2+: 3.65 μM | |||||||
24 | 31, Dolai et al. (2018) | Al3+ and Cr3+ | Turn-on/complexation (31:Al3+/Cr3+ = 1:1) | 360 nm | MeOH–HEPES buffer (4:1 v/v, pH 7.4) | Al3+: 4.3 μM | — | 65 |
Al3+: 490 nm | ||||||||
(130 nm) | ||||||||
Cr3+: 427 nm | Cr3+: 3.4 μM | |||||||
(67 nm) | ||||||||
25 | 32, Sawminathan et al. (2021) | Th4+ and Fe3+ | Turn-on/complexation (32:Th4+/Fe3+ = 1:1) | 442 nm | H2O–ACN (4:1 v/v) | Th4+: 0.27 μM | Application in solid-phase detection | 66 |
532 nm | ||||||||
(90 nm) | ||||||||
Fe3+: 5.4 μM |
To further elaborate, in a recent study, Zhou et al. utilized salicylaldehyde-derived AIE-active azine, 10, for the detection of Cu2+ ions in a turn-off manner via a metal-induced self-assembly mechanism [Fig. 3A and Table 1, entry 1].46 Upon the addition of 2 equiv. of copper ions, its fluorescence emission at 552 nm was vastly quenched (146-fold). The 10–Cu2+ complex was further employed as an S2− sensor owing to the S2−-induced disassembly of AIE-active azine (10). Other metal ions did not complex with 10 and thus they are indifferent to azine, imparting a high selectivity towards Cu2+ ions [Fig. 3B]. The images of turn-off response upon the addition of Cu2+ ions and subsequent fluorescence revival with S2− were captured under 365 nm UV light and also utilized for acquiring the fluorescence microscopy images of KYSE510 cells [Fig. 3C and D].
Fig. 3 (A) Salicylaldehyde-based azine, 10, as a turn-off chemosensor for Cu2+ ions showing 1:1 binding stoichiometry and fluorescence retrieval upon the addition of sulfide ions; (B) competitive selectivity of 10 towards different metal ions; (C) images of 10 captured upon the addition of Cu2+ ions and S2− under 365 nm UV light depicting visual fluorescence changes; (D) the change in fluorescence microscopy images of KYSE510 cells consisting of 10 after incubation with Cu2+ and Cu2+ + S2− (images B–D are adapted with permission from ref. 46. Copyright 2018, Elsevier); (E) HBT-based unsymmetrical azine (8a) as a turn-off chemosensor for Cu2+ ions showing 2:1 binding stoichiometry; (F) images of 8a captured upon the addition of Cu2+ ions and other metal ions under 365 nm UV light depicting visual fluorescence changes; (G) on-site detection tool for the TLC-strip-based sensing of Cu2+ and selectivity of 8a towards different metal ions (images F and G are adapted with permission from ref. 29. Copyright 2021, Elsevier); (H) triaminoguanidine-based azine, 11, as a turn-off chemosensor for Cu2+ ions showing 3:1 binding stoichiometry and fluorescence retrieval upon the addition of S2− ions; (I) mechanoresponsive behavior of 11 showing weak emission in pristine form and intense fluorescence in ground form; selectivity of 11 towards (J) Cu2+ ions and (K) the 11–Cu2+ complex towards S2−; (L) the reversible turn-off–on response of 11 towards Cu2+ and S2− and (M) its application in the construction of logic gates; (N) on-site detection tool for the paper-strip-based sensing of Cu2+ and S2− (images I–N are adapted with permission from ref. 47. Copyright 2019, American Chemical Society). |
We recently demonstrated the use of the benzothiazole-based unsymmetrical azine (8a) as a fluorimetric sensor for the turn-off detection of Cu2+ ions in solution and solid phase utilizing its ESIPT property [Fig. 3E and Table 1, entry 2].29 The saturation point was reached at 0.5 equiv. of Cu2+ and the stoichiometry of 8a with Cu2+ was established as 2:1 from Job's plot, EDX, time-resolved fluorescence measurements, and DFT studies. The sensing was highly selective towards Cu2+ ions and no other metal ions displayed any turn-off response [Fig. 3F]. The fluorescence of 8a can be retrieved by the addition of ascorbic acid (AA) by in situ generation of Cu+ and release of the probe from the complex. Notably, the LOD for 8a was found to be 0.005 μM, which is about 20 fold lower than Zhou et al.'s probe (10). The solid-phase sensing ability of the azine was explored using TLC plates which displayed a significant turn-off response at lower concentrations of the Cu2+ ions in a selective manner [Fig. 3G]. We demonstrated its practical applicability in real water samples with a high % recovery.
In another work, Tharmalingam et al. developed an AIE–ESIPT active star-shaped azine-based Cu2+ sensor (11) from a triaminoguanidine precursor [Fig. 3H and Table 1, entry 3].47 Its aggregation-enhanced emissive feature was exhibited in the water–ACN mixture showing an emission maximum at 470 nm. The probe, 11, displayed solvent-dependent dual emission in nonpolar and polar protic solvents, suggesting excited state ICT-coupled ESIPT characteristics. In this case, a 1:3 binding stoichiometry was observed between 11 and Cu2+ owing to the presence of three binding sites available in the structural scatffold of the chemosensor [Fig. 3H]. The azine derivative, 11, exhibited a mechanoresponsive behavior wherein the pristine sample was found to weakly fluoresce greenish yellow and the ground sample showed a bathochromic shift with fluorescence shift to intense green when observed under 365 nm UV light as well as with fluorescence microscopy [Fig. 3I]. The addition of Cu2+ resulted in a turn-off response which was found to be reversible towards S2−via a metal ion displacement method [Fig. 3J and K]. The reversible and selective on–off–on sensing characteristics of 11 toward Cu2+ and S2− were effective in the construction of an IMPLICATION logic gate [Fig. 3L and M]. The probe could also be utilized as an on-site detection tool for the paper-strip-based reversible sensing of Cu2+ and S2− ions [Fig. 3N]. Among other notable contributions on azine-based sensors for copper ions, Zhao et al. reported a tetraphenylethylene-based AIE-active azine-based compound (12) by condensation of two TPE units that could recognize Cu2+ ions in a turn-off manner [Table 1, entry 4].26 The introduction of the azine unit as an electron acceptor could inculcate a bathochromic shift from blue (about 465 nm for typical TPE emission) to orange emission (λmax 581 nm). The probe functioned well as a selective copper ion sensor by 1:1 complexation and offered an LOD of 0.03 μM. Similarly, Tiwari et al.,48 Ye et al.,49 Liu et al.,50 Kumarasamy et al.,51 and Sharifi et al.52 demonstrated different symmetrical and unsymmetrical azine-based probes (10a, 13–16) with emission in the blue to green region for the detection of Cu2+ ions [Table 1, entries 5–9].
Kumar et al. synthesized a symmetrical azine (17) based on benzophenone and studied its application in the detection of Al3+ ions [Table 1, entry 10].53 The probe, 17, exhibited weak emission in MeOH due to intramolecular rotations and a typical AIE behavior in >70% H2O–CH3CN resulting in intense emission. The azine could detect Al3+ in a turn-on manner in MeOH with a limit of detection of 0.27 μM, along with a notable colorimetric response. The binding of Al3+ with 17 restricted the intramolecular rotation and caused enhancement in emission. The stoichiometry was studied by mass spectrometry, NMR titration and Job's plot, which suggested a 1:1 ratio of 17:Al3+ in the complex. In another study, Nguyen et al. synthesized a salicylaldehyde-derived water-soluble azine (18) having terminal sulphonate functionalities to detect Al3+ in aqueous solutions [Table 1, entry 11].27 The sulfonate functional groups in the scaffold provide an enhanced water-solubility to the probe. The complexation of Al3+ with 18via the azine –N atom and phenolic –OH causes an aggregation-induced emission enhancement (AIEE) at λmax 511 nm leading to the formation of well-defined dendritic structures. 18 displayed high selectivity towards Al3+ ions with a moderate detection limit of 0.153 μM. Only a 15% response towards other metal cations such as Zn2+ and Pb2+ was observed at high concentrations of these analytes indicating selectivity towards Al3+ ions. Further, 18 was incorporated into a digital microfluidic sensor chip, resulting in a sub-micromolar portable detection system for water samples contaminated with Al3+. In another study in the similar direction, Khanra et al. synthesized 4-(anthracen-9-ylmethylene-hydrazonomethyl)-2-methoxy-phenol (19) and utilized it as a turn-on fluorimetric sensor for Al3+ detection in sodium dodecyl sulphate (SDS) medium [Table 1, entry 12].54
Khanra et al. further reported a β-naphthol derived azine-based chemosensor (20) for the detection of Zn2+ ions at the nano-molar level [Table 1, entry 13].55 The chelation of Zn2+ ions with 20 results in chelation-enhanced fluorescence (CHEF) through inhibition of ESIPT and –CN– isomerization and an enhanced emission was observed at 495 nm. The probe displayed negligible CHEF in the presence of other metal ions and showed a detection limit as low as 36.16 nM. The Job's plot and mass analysis confirmed a 1:1 binding stoichiometry between 20 and Zn2+ ions. In contrast, Das et al. reported a turn-on fluorescence sensor using a salicylaldehyde derived azine (21) for the selective determination of Zn2+ in the presence of acetate ions (AcO−). The probe exhibited very weak fluorescence. Its emission intensity increases at λmax 532 nm in the presence of Zn2+ over several other metal ions, and the emission profile is augmented only when AcO− is present as the counter anion. They proposed that the addition of Zn2+ triggers a synergistic effect and results in pronounced fluorescence enhancement attributed to the Zn2+ assisted CHEF process, and inhibition of the PET and ESIPT process [Table 1, entry 14].56 The binding of Zn2+ associated with AcO− ions locks the free rotation around the –CN– resulting in the suppression of the non-radiative decay process in the excited state giving strong emission.
Musikavanhu et al. derived a naphthol-based azine attached with thiophene (22) for the purpose of detecting trivalent chromium (Cr3+) [Table 1, entry 15].57 The turn-off response at λmax 526 nm with a low detection limit of 0.041 μM can be attributed to the fact that Cr3+ is a paramagnetic fluorescence quencher having empty d-shells. Also, the ligand-to-metal charge transfer (LMCT) results in chelation-enhanced quenching (CHEQ). Azine 22 was highly selective towards Cr3+ as compared to other competing metal ions owing to Pearson's hard and soft acids and bases (HSAB) theory that defines the greater affinity of hard acid, Cr3+, towards the electron donating imine nitrogen than others.
Manigandan et al. reported a symmetrical 4-hydroxy-3-methoxybenzaldehyde-derived azine probe (23) as a highly reliable Fe3+ sensor [Table 1, entry 16].28 In 1:1 DMF–H2O, the blue emissive azine (λem 423 nm) exhibits a sensitive fluorescence “turn-off” response towards Fe3+ ions with a limit of detection of 0.077 μM. The azine, 23, displayed high selectivity towards Fe3+ ions over other metal ions except for La3+ and Fe2+ ions which also showed an appreciable decrease in fluorescence intensities. The energy or electron transfer processes leading to the reverse photo-induced electron transfer process and the paramagnetic property of Fe3+ ions along with the unfilled d subshell contributed to the fluorescence quenching of 23.
Recently, Mondal et al. developed a pyrene-hydroxyquinoline-based azine (24) for selective turn-on detection of toxic Hg2+ ions [Table 1, entry 17].58 In EtOH–H2O (9:1) medium, 24 showed a turn-on response towards Hg2+ ions with a detection limit of 0.22 μM. The probe, 24, is weakly emissive in 9:1 EtOH–H2O medium and upon the addition of Hg2+ ions, it undergoes enhancement that is attributed to the CHEF effect owing to metal–ligand complexation which further triggers the aggregation of the complex and the AIEE effect dominates at higher Hg2+ concentrations. The DFT studies indicated that probe 24 acts as a tridentate ligand engaging one of the azine –N atoms, the quinoline –N atom and the –OH group to specifically bind to Hg2+. In another study, Tong et al. synthesized a series of azine compounds (25) and utilized them for the turn-on detection of Hg2+ ions [Table 1, entry 18].59
Ghosh et al. utilized a salicylaldehyde-based weakly fluorescent azine (26) for the detection of Mo6+ ions in an EtOH–H2O (9:1) medium [Table 1, entry 19].60 The planar geometry of 26 favors the PET process involving electron transition from imine –N to the conjugated aldehyde moiety and fluoresces weakly at 415 nm. A ratiometric response is observed with a decrease in peak at 415 nm and a simultaneous increase at 501 nm upon the addition of Mo6+ ions. The 26:Mo6+ complex restricts the PET process, leading to CHEF. The formation of a 1:2 complex between 26 and Mo6+ was observed with a detection limit as low as 0.002 μM. The sensor was applied for the measurement of Mo6+ in certified steel samples. The selective extraction of Mo6+ from a mixture with other common metal ions using 26 was particularly effective.
Similarly, Pham et al. developed a highly selective and sensitive azine-based probe (27) for the turn-off detection of uranyl ions in an organoaqueous media [Table 1, entry 20].61 The addition of UO22+ ions to 27 in 80% water–ACN fractions resulted in a small decrease in fluorescence intensities, whereas at 60% water fractions, a significant fluorescence quenching was noted. Similarly, the addition of UO22+ ions to the unsubstituted azine scaffold did not alter the emission to the extent that was possible with the presence of the –NO2 group in 27. This was attributed to the electron-withdrawing effect of –NO2 groups which stabilize the phenolate form of 27 in solution and the complexation with UO22+ ions was more efficient. The complexation of 27 with UO22+ ions destroyed the aggregation of the probe to solubilize the molecules in the solution resulting in a turn-off response with a 27:UO22+ complexation stoichiometry of 1:1.
Some azine-based probes with dual metal ion detection ability have also been reported. Yadav et al. demonstrated an unsymmetrical azine (28) derived from 2-hydroxynaphthalene that exhibits viscochromic and mechanochromic properties and detects Al3+ and Cu2+ ions via two different sensing pathways in DMSO:HEPES:MeOH (0.1:1.9:8.0, v/v, HEPES buffer, pH 7.4) [Table 1, entry 21].62 At the outset, a fluorescence turn-on and turn-off mechanism having 1:1 binding stoichiometries was displayed upon the addition of Al3+ and Cu2+ with LODs of 0.165 μM and 0.152 μM, respectively. The stable 28:Al3+ complex formation imparts rigidity resulting in the CHEF effect, which subdues the PET process from the –N atom of azine to the large π-conjugation of the naphthalene moiety, thereby affording an increase in fluorescence intensity. Similarly, the turn-off response with Cu2+ is owing to the strong paramagnetic property of Cu2+ with a partially filled d-shell showing a high affinity for 28 with N or O as coordinating atoms. The binding of Cu2+ leads to CHEQ as the excited state of the fluorophore is suppressed by ligand-to-metal charge transfer (LMCT). F− and EDTA2− ions made 28 reversible for Al3+ and Cu2+ ions. Similarly, Sun et al. synthesized a series of azine derivatives (29) which displayed a turn-on response towards Al3+ in DMSO–H2O (4:1) and a turn-off response towards Cu2+ in DMSO–H2O (3:7) [Table 1, entry 22].63
A naphthol-based fluorescent probe, 30, was demonstrated by Das et al. for the distinguishable turn-on detection of Al3+ and Zn2+ in different solvent systems (Al3+ in MeOH–H2O (9:1) and Zn2+ in DMSO–H2O (9:1)) [Table 1, entry 23].64 In the less polar MeOH–H2O solvent system, Al3+ forms a strong complex with the hard oxophilic donor owing to its small size and high charge. At the same time, 30 is more nucleophilic by capturing the acidic O–H proton in the strong polar solvent DMSO–H2O. Al3+ is strongly passivated by DMSO–H2O compared with Zn2+, thereby making Zn2+ readily available for metal complex formation in the highly-polar solvent. In a similar manner, Dolai et al. utilized a weakly emissive salicylaldehyde-based azine probe (31) for the turn-on detection of Cr3+ and Al3+ by two distinct outputs [Table 1, entry 24].65 The addition of Cr3+ and Al3+ to 31 resulted in fluorescence enhancement at two different wavelengths (427 nm for Cr3+ and 490 nm for Al3+) which is attributed to the CHEF effect and the ICT (intermolecular charge transfer) between the metal ions (Al3+ and Cr3+) and 31. This in turn is due to the different radii of the two metal ions as well as the different ionic potentials (electronic charge/radius of ions).
Sawminathan et al. presented a dual-emission responsive azine-based chemosensor (32) that uses a colorimetric and fluorescence turn-on technique to quickly, sensitively and selectively detect Th4+ and Fe3+ [Table 1, entry 25].66 When exposed to Th4+/Fe3+, the non-emissive 32 emits yellow fluorescence and it offers low detection limits of 2.1 nM and 3.3 nM for Th4+ and Fe3+, respectively. Initially, 32 is non-emissive due to the PET phenomenon that occurs from the electronegative –N atom to the highest occupied molecular orbital (HOMO) of the excited fluorophore. However, the addition of Th4+/Fe3+ results in turn-on response by blocking the PET process. Paper strips were made using 32 and their ability to sense Th4+ and Fe3+ in the solid phase was demonstrated. As real samples, several water bodies and human serum albumin were used to successfully assess the performance of 32 in detecting Th4+/Fe3+ ions.
Among recent developments, Shen et al. synthesized a diphenylphosphinate-protected salicylaldehyde-based azine chemodosimeter (33) and utilized it for the detection of peroxynitrite (ONOO−) ions [Fig. 4A and Table 2, entry 1].73 The ONOO− ions could cleave the diphenylphosphinate group to afford the green fluorescent salicylaldehyde azine (λmax 520 nm) back in the solution to offer turn-on sensing for ONOO− ions [Fig. 4A]. The probe, 33, could detect endogenous ONOO− ions with high selectivity and excellent sensitivity and demonstrated a low detection limit of 0.08 μM [Fig. 4B]. The probe was further investigated for its ability to image ONOO− in living cells and it was found that the probe could specifically detect endogenous ONOO− in HeLa cells [Fig. 4C]. Yuan et al. synthesized another azine-based probe (34) for the detection of F− ions by incorporating 2-hydroxy-1-naphthaldehyde and 1,8-naphthalimide [Fig. 4D and Table 2, entry 2].74 In the presence of F− ions, 36 results in a color shift from yellow to light purple along with a fluorescence change in a turn-off manner [Fig. 4E]. The 1H NMR titration revealed that 36 undergoes deprotonation of phenolic –OH via a hydrogen-bond interaction between phenolic OH− and F− ions. The deprotonation blocks the ESIPT process and tautomerization from the enol form to keto form occurs which induces the PET effect in the system.
Fig. 4 (A) Diphenylphosphinate modified salicylaldehyde-based azine (33) as a turn-on chemodosimeter for ONOO− ions by cleavage of the diphenylphosphinate group; (B) selectivity of 33 against different analytes depicting high selectivity towards ONOO− ions; (C) fluorescence microscopy images of HeLa cells in the presence of 33 and ONOO− ions (images B and C are adapted with permission from ref. 73. Copyright 2019, Elsevier); (D) naphthalimide-based azine (34) as a turn-off chemodosimeter for F− ions by the deprotonation strategy; (E) selectivity studies depicting a change in color from yellow to light purple and fluorescence quenching in the presence of F− ions (adapted with permission from ref. 74. Copyright 2018, Elsevier). |
Sr. no. | Probe | Analyte | Mechanism/strategy | λ ab | Solvent system | LOD | Remark | Ref. |
---|---|---|---|---|---|---|---|---|
λ em | ||||||||
(Δλ nm) | ||||||||
1 | 33, Shen et al. (2019) | ONOO− | Turn-on/diphenyl phosphinate cleavage | 403 nm | DMSO–PBS buffer (1:99 v/v, 50 mM, pH 7.4) | 0.08 μM | — | 73 |
520 nm | ||||||||
(117 nm) | ||||||||
2 | 34, Yuan et al. (2018) | F− | Turn-off/deprotonation | 420 nm | THF | 0.015 μM | — | 74 |
593 nm | ||||||||
(173 nm) | ||||||||
3 | 35a, R = H | CN− | Turn-on/nucleophilic addition | 320 nm | ACN | 0.058 μM | — | 75 |
35b, R = Me | 440 nm | |||||||
35c, R = F | (120 nm) | |||||||
35, Devendhiran et al. (2021) | ||||||||
4 | 36, Yao et al. (2022) | CN− | Turn-off/deprotonation | 413 nm | H2O–DMSO (3:2 v/v) | 0.01 μM | Fluorescence retrieval with H+ | 76 |
562 nm | ||||||||
(149 nm) | Application in solid-phase detection | |||||||
5 | 37, Paul et al. (2023) | CN− | Turn-on/deprotonation | 365 nm | ACN–HEPES buffer (99:1 v/v, pH 7.3) | 0.045 μM | Solid state fluorescence quenching with TFA vapors and reversible with TEA vapors | 77 |
565 nm | ||||||||
(200 nm) | ||||||||
6 | 38a, R1 = R2 = H | ClO− | Turn-on/deprotonation | 350 nm | DMSO–PBS buffer (1:4 v/v, pH 7.4) | 0.05 μM | Application in solid-phase detection | 78 |
38b, R1 = OH, R2 = H | 530 nm | |||||||
38c, R1 = OH, R2 = Me | (180 nm) | |||||||
Singh et al. (2020) |
Devendhiran et al. reported a series of coumarin-based azines (35) and utilized them for the selective and sensitive turn-on detection of CN− ions [Table 2, entry 3].75 The probe works as a turn-off sensor by nucleophilic addition of the ions across the azine double bond with a detection limit of 0.058 μM. Similarly, Yao et al. developed a naphthalene-based unsymmetrical azine (36) to detect CN− in aqueous media via a turn-off fluorescence response resulting from the deprotonation of phenolic –OH [Table 2, entry 4].76 The probe, 36, recognizes CN− with good selectivity and sensitivity displaying an LOD of 0.01 μM. Paul et al. demonstrated a naphthalene hydrazone-based unsymmetrical azine (37) as a turn-on sensor for the detection of CN− ions [Fig. 5A and Table 2, entry 5].77 Azine 37 displayed typical AIE characteristics, having weak emission at 503 nm in ACN and the highest emission intensity at 80% water fractions with a bathochromic shift from 503 nm to 537 nm [Fig. 5B]. The probe was utilized for the turn-on detection of CN− ions in ACN–HEPES buffer. The sensing mechanism is based on the deprotonation by the mild base CN− to facilitate an extensive delocalization of charge between phenolate –O− and the aromatic rings in the planar form leading to fluorescence enhancement. They also proposed that the cleavage of the intramolecular hydrogen bonding might stop the ESIPT. The probe showed high sensitivity towards CN− ions with a limit of detection of 45.4 nM [Fig. 5C] with a high selectivity against most other interfering anions [Fig. 5D]. Azine 37 showed intense emission in the solid state and was therefore utilized for the sensitive detection of trifluoroacetic acid (TFA) vapors via fluorescence quenching with an LOD of 1.41 ppm [Fig. 5E]. The protonation-driven destruction of compacted arrangement in the solid state was assumed to be the quenching mechanism of 37. The turn-off system was further utilized for the reversible acidochromic behavior upon the sequential addition of triethylamine vapors [Fig. 5F]. The probe, 37, was reversible with TFA and triethylamine (TEA) and the system could easily be recycled several times, demonstrating its potent reusability [Fig. 5G].
Fig. 5 (A) Naphthalene-based azine (37) as a turn-on chemodosimeter for CN− ions by the deprotonation strategy; (B) AIE behavior exhibited by 37 with the highest intensity at 80% water fractions; (C) turn-on response of 37 upon the addition of CN− ions in 99% ACN; (D) selectivity of 37 against different analytes; (E) turn-off response of 37 upon the addition of TFA vapors in the solid state; (F) reversibility of the turn-off–on mechanism against addition of TFA followed by TEA; (G) reusability study of 37 against TFA vapors and TEA vapors showing high sensitivity and accuracy even after 6 cycles (adapted with permission from ref. 77. Copyright 2023, Royal Society of Chemistry). |
Singh et al. demonstrated a few azine-based sensors (38) for the reversible detection of hypochlorite in aqueous media employing the protonation–deprotonation strategy [Table 2, entry 6].78 The AIE–ESIPT-active assemblies of salicylaldehyde/indolium-based probes (38a) displayed sensitive detection of hypochlorite with a detection limit of 0.052 μM. The highly sensitive response to ClO− ions was owing to the elevated acidity and the formation of more organized structures following deprotonation. Additionally, the ‘dip strip’ of 38a has been used to show the real-time use for ‘on-site’ solid-phase detection of hypochlorite. Moreover, these assemblies were effectively employed for visualizing hypochlorite within cells and acted as antioxidants to avert cell death induced by hypochlorite.
In recent times, Sathiyaraj et al. synthesized a short series of N,N-dimethylaminobenzaldehyde-based symmetrical azines (39) having electron-donating amino substituents as the recognition sites for the detection of nitro explosive, picric acid [Table 3, entry 1].89 The donor–π–donor probe displayed high selectivity in an aggregated form which arises from the substituents at the amine group. Notably, picric acid enhanced the fluorescence of the azine monomers in pure THF but quenched the same in the THF–water mixture. In THF, picric acid forms a hydrogen bonding network with one of the amine nitrogen atoms, resulting in an electron-accepting group instead of an electron donor. Further, the fluorescence quenching with PA was attributed to the inner filter effect and the disturbance of aggregates by the hydrogen bonding interaction between the nitrogen of PA and N,N-dialkylamino group. Similarly, our group utilized the red-emissive HBT-based unsymmetrical dyes, 8d, for the detection of nitroaromatic compounds (NACs) [Table 3, entry 2].37 The electron-deficient NACs in particular, picric acid, undergo noncovalent interactions with electron-rich azines resulting in the turn-off detection of NACs [Fig. 6A]. The disruption in the aggregation is due to the intercalation of nitroaromatics in an ordered array of 8 by more favorable π–π interactions. The red-emissive azine with the highest emission maxima, 8d, exhibited a turn-off response towards PA in 1:19 v/v DMF–H2O with a limit of detection of 0.09 μM. The probe, 8d, displayed variable responses to other NACs such as 2,4-dinitro-chlorobenzene and 4-nitrotoluene and was non-responsive against other aromatic compounds with no or insignificant turn-off response [Fig. 6B].
Sr. no. | Probe | Analyte | Mechanism/strategy | λ ab | Solvent system | LOD | Remark | Ref. |
---|---|---|---|---|---|---|---|---|
λ em | ||||||||
(Δλ nm) | ||||||||
1 | 39a, R = Me | Picric acid | THF: turn-on, hydrogen bonding | THF: 415 nm | THF or H2O–THF (7:3 v/v) | THF: 26 μM | — | 89 |
570 nm | ||||||||
(155 nm) | ||||||||
39b, R = Et | H2O–THF: turn-off, protonation at azine N | H2O–THF: 443 nm | H2O–THF: 38 μM | |||||
39c, R = Pr | 490 nm | |||||||
39d, R = Ph | (47 nm) | |||||||
Sathiyaraj et al. (2020) | ||||||||
2 | 8d, Bhosle et al. (2023) | NACs | Turn-off/disruption of AIE property by intercalation of NACs | 398 nm | H2O–DMF (19:1 v/v) | 0.09 μM | Application in solid-phase detection | 37 |
675 nm | ||||||||
(277 nm) | ||||||||
3 | 40, Bhosle et al. (2022) | H2O2 | Turn-on/benzyl boronic acid cleavage | 384 nm | DMSO–PBS buffer (0.1:9.9 v/v, 10 mM, pH 7.4) | 0.039 μM | Application in solid-phase detection | 90 |
617 nm | ||||||||
(233 nm) | ||||||||
4 | 41, Song et al. (2018) | Cys | Turn-on/dinitro benzene sulphonyl cleavage | 405 nm | DMSO–PBS buffer (1:9 v/v, 10 mM, pH 7.4) | 2.84 μM | Application in solid-phase detection | 91 |
547 nm | ||||||||
(142 nm) | ||||||||
5 | 42, Bhattu et al. (2023) | Azinphos-methyl | Turn-on/H-bonding interactions | 275 nm | H2O | 7.4 μM | — | 92 |
355 nm | ||||||||
(80 nm) | ||||||||
6 | 43, Thiagarajan and co-workers (2021) | Diethylchlorophosphate (DCP) | Turn-on/ACN: nucleophilic substitution at azine N | ACN: 373 nm | ACN or 80% H2O–ACN (4:1 v/v) | ACN: 0.0099 μM | — | 93 |
495 nm | ||||||||
(122 nm) | ||||||||
ACN–H2O: protonation at azine N | ACN–H2O: 269 nm | ACN:H2O: 0.068 μM | ||||||
432 nm | ||||||||
(163 nm) | ||||||||
7 | 44, Sathiyaraj et al. (2020) | Diethylchlorophosphate (DCP) | Turn-on/THF: nucleophilic substitution at azine N | THF: 440 nm | THF or H2O: THF (7:3 v/v) | THF: 0.2 μM | — | 94 |
513 nm | ||||||||
(73 nm) | ||||||||
THF:H2O: protonation at azine N | THF:H2O: 368 nm | THF:H2O: 106 μM | ||||||
570 nm | ||||||||
(202 nm) | ||||||||
8 | 45, He et al. (2020) | Alkaline phosphatase (ALP) | Turn-on/phosphate cleavage | 356 nm | 50 mM Tris buffer, pH 9 | 0.012 U L−1 | — | 95 |
536 nm | ||||||||
(180 nm) | ||||||||
9 | 46, Tong and co-workers (2018) | β-Lactamase | Turn-on/dinitro benzene sulphonyl cleavage | 400 nm | PBS buffer (10 mM, pH 7.4) | 0.5 mU mL−1 | NA | 96 |
558 nm | ||||||||
(158 nm) | ||||||||
10 | 47, Chang et al. (2022) | Neuraminidase (NA) | Turn-on/sialic acid cleavage | 387 nm | 10 mM PBS buffer (pH 7.4) | 0.024 U mL−1 | — | 97 |
524 nm | ||||||||
(137 nm) |
Fig. 6 (A) HBT-based unsymmetrical azine dye (8d) as a turn-off chemosensor for the sensitive detection of nitroaromatic compounds showing a turn-off response by disruption in AIE owing to the intercalation of NACs; (B) the fluorimetric responses of 8d against different analytes depicting the high selectivity of 8d towards NACs (images A and B are adapted with permission from ref. 37. Copyright 2023, Wiley-VCH); (C) HBT-based chemodosimeter (40) for the detection of H2O2 ions by cleavage of the benzylboronic acid group; (D) turn-on detection of H2O2 ions by 40 with a low detection limit; (E) demonstration of solid-phase detection of H2O2 using TLC plates and ImageJ analysis for on-site quantitation of H2O2; (F) fluorescence microscopy images of HeLa cells in the presence of 40 and H2O2 ions (images C–F are adapted with permission from ref. 90. Copyright 2022, Elsevier). |
Our group further utilized one of the benzothiazole-derived unsymmetrical azines with a p-Cl substituent (8) and protected it with a benzyl boronic acid group as the recognition unit for the selective detection of H2O2 ions to afford a turn-on chemodosimeter [Fig. 6C and Table 3, entry 3].90 H2O2 spontaneously cleaves the benzyl boronic acid group of the chemodosimeter (40) in 1% DMSO in PBS (10 mM, pH 7.4) medium to produce its precursor 8, which emits intense orange AIE [Fig. 6D]. The probe was non-responsive to other ROS, cations, anions, oxidizing, and reducing agents. The high sensitivity of 40 towards H2O2 is attributed to a low limit of detection (LOD) of 3.9 × 10−8 M (1.3 ppb). The practical utility of 40 in H2O2 detection was demonstrated by spiking H2O2 in water samples collected from local water bodies and in blood serum. Azine 40 was successfully demonstrated in solid-phase detection of H2O2 using TLC plates as the platform, a smartphone for image-capturing, and ImageJ analysis for a practical demonstration of the on-site quantitation of H2O2 [Fig. 6E]. The probe, 40, could efficiently detect intracellular H2O2, as shown by imaging in live HeLa cells [Fig. 6F].
Song et al. developed a salicylaldehyde-based azine chemodosimeter, 41, protected with a dinitrobenzene sulphonyl group for the detection of Cys/Hcy in a turn-on manner [Table 3, entry 4].91 The addition of Cys/Hcy to the probe solution resulted in the cleavage of the 2,4-dinitro benzenesulfonate group of 41 to afford the turn-on response. The probe, 41, displayed a significant Stokes shift (148 nm), low cytotoxicity, and good photostability. It was further utilized as a portable kit for the on-site inspection of more than ten micro samples simultaneously which might successfully reduce the development of false positives and visual errors. In addition, it was also demonstrated for cell imaging using PC12 cells, establishing its potential in the detection of Cys/Hcy in live cells.
Azinphos-methyl (Guthion) is a broad spectrum organophosphate (OPP) insecticide and an acetylcholinesterase inhibitor. It is classified as an extremely hazardous substance by US-EPA making its sensitive detection as an important task. Bhattu et al. synthesized azine nanoparticles (E)-(4-chlorophenyl)-1,1-diamino-2,3-diazabutadiene (42) and utilized them for the detection of azinphos-methyl under aqueous conditions [Fig. 7A and Table 3, entry 5].92 H-bonding interactions between the analyte and guanidine-like unit of the probe, 42, were responsible for the selective turn-on detection of azinphos-methyl [Fig. 7B]. It showed a limit of detection of 7.4 μM. Its application in real samples like orange juice, water samples, etc. showed good recovery and selective fluorescence response. Thiagarajan's group synthesized a new unsymmetrical azine, 43, and utilized it for the selective and sensitive turn-on detection of the nerve agent mimic diethylchlorophosphate (DCP) by two different mechanisms in different solvent systems [Table 3, entry 6].93 The photoinduced electron transfer results in a turn-on emission at 495 nm in ACN due to nucleophilic substitution of DCP at the azine nitrogen close to the –OMe group giving rise to a new ICT state [Fig. 7C]. A 1763-fold enhancement in fluorescence was observed with a low detection limit of 9.9 nM. Contrastingly, the protonation at the azine nitrogen in an ACN:H2O (1:4) mixture increased the fluorescence at 422 nm by 1188-fold with a limit of detection of 68 nM [Fig. 7D]. DCP sensing was also demonstrated on TLC strips and polymethylmethacrylate (PMMA) polymer film by coating the probe solution on the solid platforms and then recording the images in the presence and absence of DCP vapors under 365 nm UV light [Fig. 7E]. The absence of DCP vapors showed no fluorescence emission, however, the addition of DCP vapors afforded a green fluorescence indicating the potential of 43 to detect DCP vapors qualitatively from the environmental samples in solid platforms. The same group developed an unsymmetrical D–π–A type azine, 44, for the detection of DCP by two different channels [Table 3, entry 7].94 The probe, 44, forms a new ICT state with DCP in pure THF by phosphorylation at the imine nitrogen close to the donor moiety of 44. This results in color change to orange with a 203-fold fluorescence enhancement at 513 nm and this moiety acts as a strong withdrawing group. Azine 44 displayed intense fluorescence emission at 570 nm in THF–H2O fractions which undergoes protonation at the amine nitrogen upon the addition of DCP and causes a blue-shifted emission to 406 nm and fluorescence quenching at 570 nm. The probe also functions as a test-strip based detection assay to detect DCP vapors using Whatman filter paper which displays a visual color change of the test strip from yellow to orange immediately after exposure to DCP vapors.
Fig. 7 (A) 1,1-Diaminoazine (42) as a chemosensor for organophosphorus pesticide azinphos-methyl; (B) selectivity study of 42 against various OPPs and metal ions (images A and B are adapted with permission from ref. 92. Copyright 2023, Elsevier); salicylaldehyde-based azine (43) as a dual-mode chemodosimeter for the detection of nerve agent mimic diethylchlorophosphate (DCP) by (C) turn-on emission at 495 nm in ACN due to nucleophilic substitution of the DCP at the azine nitrogen close to the –OMe group giving rise to a new ICT state and (D) turn-on emission at 422 nm due to protonation at the azine nitrogen in an ACN:H2O mixture; (E) DCP sensing demonstrated on TLC strips and PMMA polymer film showing green fluorescence emission in the presence of DCP vapors under 365 nm light (images C–E are adapted with permission from ref. 93. Copyright 2021, Elsevier). |
He et al. reported a phosphate-protected salicylaldehyde-based azine (45) and utilized it for the detection of alkaline phosphatase in aqueous medium [Fig. 8A and Table 3, entry 8].95 Additionally, 45 demonstrated strong water solubility and rapid response with a large Stokes shift. The addition of ALP resulted in more than 240-fold turn-on emission intensities [Fig. 8B]. The selectivity study confirmed the sensitive response of 45 towards ALP and no significant change was observed when it is exposed to metal ions, reactive oxygen species, reactive sulfur species (Cys, Hcy, and GSH) and enzymes (esterase, trypsin and lysozyme) [Fig. 8C]. ALP eliminates the phosphate groups of 45 by dephosphorylation affording an intermediate compound that contains one phosphate group and shows very weak fluorescence. The intermediate then undergoes the second dephosphorylation step and releases the unprotected salicylaldehyde-based azine which forms aggregates owing to the intramolecular hydrogen bond and increased hydrophobicity leading to a strong fluorescence signal due to the combined AIE and ESIPT mechanism. Azine-based probe 45 was further explored for differentiating the intracellular ALP activity in different cell lines such as MG-63, WI-38, B6F10, RAW264.7 and HEK293. It was found that MG-63 cells displayed the strongest fluorescence, indicating the highest expression level of ALP in MG-63 cells. WI-38, B16F10 and RAW 264.7 cell lines showed a moderate response, whereas a negligible response was displayed with HEK 293 cells [Fig. 8D]. In addition, MG-63 cells were investigated for the inhibition effect of the ALP inhibitor. The use of 1 mM Na3VO4 as an inhibitor showed negligible fluorescence intensity indicating that dephosphorylation of the ALP activity was inhibited by Na3VO4 [Fig. 8E].
Fig. 8 (A) Salicylaldehyde-based azine (45) as a chemodosimeter for alkaline phosphatase by cleavage of the phosphate group; (B) turn-on detection by fluorescence enhancement at 536 nm upon incremental addition of ALP; (C) change in fluorescence intensities towards ALP and various interfering analytes; confocal images of (D) MG-63, WI-38, B16F10, RAW 264.7 and HEK 293 cells after incubation with 45 showing intense fluorescence emission with MG-63 cells indicating the highest ALP expression and (E) MG-63 cells incubated with 45 in the absence and presence of 1 mM Na3VO4 wherein the inhibitor results in negligible turn-on response (images A–E are adapted with permission from ref. 95. Copyright 2020, Royal Society of Chemistry); (F) 2,4-dinitrobenzenesulfonyl protected salicylaldehyde-based azine (46) as a chemodosimeter for β-lactamase; (G) AIE–ESIPT behavior exhibited by the azine precursor; (H) turn-on detection of β-lactamase by fluorescence enhancement at λmax 558 nm; (I) fluorescence response of 46 towards different metal ions, proteins, enzymes, etc. confirming the high selectivity of 46 towards β-lactamase; (J) demonstration of solid-phase detection of β-lactamase on paper-strips; (K) demonstration of solid-phase detection of GSH and β-lactamase in milk samples on paper-strips (images F–K are adapted with permission from ref. 96. Copyright 2018, Royal Society of Chemistry). |
Tong's group utilized another non-fluorescent azine probe, 46, protected with a dinitrobenzene sulphonyl group for β-lactamase detection wherein the analyte first reacts with the substrate's lactam (cefazolin sodium) to form a secondary amine, commencing a spontaneous elimination event and yielding a thiol molecule [Fig. 8F and Table 3, entry 9].96 The thiol reacted with the sulfonate group of 46 to release the salicylaldehyde azine derivative which exhibited AIE–ESIPT properties [Fig. 8G]. β-Lactamase fluorescence measurement afforded a turn-on response at 558 nm with a detection limit of 0.5 mU mL−1 [Fig. 8H]. The probe, 46, was highly selective towards β-lactamase and no other analyte resulted in significant fluorescence emission [Fig. 8I]. Further, 46 was utilized as a portable test paper sensor for the detection of β-lactamase by dipping the filter paper strips coated with 46 into the sample solution containing cefazolin (4.8 mM) and different concentrations of β-lactamase (0–7.0 mU mL−1). A good linearity was obtained in the β-lactamase concentration range of 0–2.0 mU mL−1 [Fig. 8J]. 46 was also investigated for β-lactamase content in milk samples and the results showed good recoveries, suggesting the potential use for β-lactamase detection in milk samples [Fig. 8K].
Chang et al. demonstrated a dual sialic acid-protected salicylaldehyde-derived azine, 47, for the detection of neuraminidase (NA), a crucial enzyme for the replication of the influenza virus [Fig. 9A and Table 3, entry 10].97 The initially non-fluorescent probe 47 displayed a turn-on emission at 524 nm with a 30-fold fluorescence enhancement upon the addition of NA having a limit of detection of 0.024 U mL−1 due to the cleavage of the sialic acid group [Fig. 9B]. Azine 47 was further explored to detect the influenza virion using hemagglutination (HA) titer for the relative concentration of the virus. H3N2 viruses with different HA titers displayed enhanced fluorescence emission with the increment of H3N2 virions with an LOD of 2−1 HAU per 50 μL [Fig. 9C]. The probe 47 in combination with oseltamivir carboxylic acid (OC) was explored to distinguish oseltamivir-resistant mutant type NA (drug-resistant influenza virus strains) from wild types. It was observed that wild-type NA (WT) inhibited the hydrolysis of 47 in the presence of OC, whereas H274Y mutant NA (MT) hydrolyzed 47 both in the presence and absence of OC [Fig. 9D]. The probe, 47, was employed for NA detection in MDCK cells infected by the influenza virus. MDCK cells infected with H3N2 displayed high fluorescence under confocal imaging whereas the presence of OC showed extremely low background fluorescence [Fig. 9E].
Fig. 9 (A) Salicylaldehyde-based azine, 47, as a chemodosimeter for the detection of neuraminidase (NA) by cleavage of the sialic acid group; (B) turn-on emission at 524 nm upon addition of NA; (C) turn-on emission at 524 nm upon the addition of different concentrations of H3N2 viruses; (D) fluorescence intensities of 47 after addition of NA showing fluorescence quenching of wild type (WT) in the presence of OC; (E) fluorescence imaging in mock-infected (a), H3N2 infected (b) and OC pretreated infected MDCK cells (c) (adapted with permission from ref. 97. Copyright 2022, Elsevier). |
Fig. 10 (A) NIR-emissive cationic azine (48) as a dual-chemodosimeter for N2H4 and HSO3− ions; (B) turn-off detection of HSO3− ions by addition across the double bond of the azine; (C) ratiometric response in the presence of N2H4 by cleavage of the cyano pyridyl group; demonstration of solid-phase detection of (D) N2H4 and (E) HSO3− ions; (F) demonstration of vapor-phase detection of N2H4; (E) fluorescence microscopy images of A549 cells in the presence of 48 and (G) N2H4 and (H) HSO3− ions (adapted with permission from ref. 30. Copyright 2023, Elsevier). |
Fig. 11 (A) The fluorometric responses of 49 against various metal ions captured under 365 nm UV-light showing selective turn-on response towards Zn2+ ions; (B) turn-on fluorescence response of 49 at 500 nm upon incremental addition of Zn2+ ions; (C) the change in the fluorescence emission of 49 at various DMF:glycerol mixtures and its corresponding images captured under 365 nm UV-light showing stronger emission at higher glycerol fractions; (D) the fluorimetric changes displayed by 49 as a function of pH captured under 365 nm UV-light; (E) the reversible behavior of 49 demonstrated against NaOH and HCl showing high reusability up to 4 cycles; fluorescence microscopy images of SiHa cells studied against (F) pH variation, (G) Mito tracker activity and (H) Zn2+ detection (adapted with permission from ref. 99. Copyright 2022, Royal Society of Chemistry). |
Ganesan et al. synthesized a symmetrical azine 4,4′-((1E,1′E)-hydrazine-1,2-diylidenebis(methanylylidene)) diphenol (50) from 4-hydroxybenzaldehyde and utilized it for a 1:1 inclusion complex formation with γ-cyclodextrin [Fig. 12A].103 The azine, 50, displayed poor water solubility, and thus resulted in weak fluorescence emission. The inclusion complexation of γ-CD/50 in an aqueous medium increased the water solubility and favored the metal ion sensing phenomenon. The fluorescent assembly was able to detect Al3+ selectively and sensitively in the presence of different analytes. The formation of a stable 1:1 complex with Al3+ which predominantly uses their –OH and –N atoms afforded an LOD of 1.67 nM. The probe, 50, was further employed for fluorescence microscopy imaging which displayed a fluorescence quenching phenomenon upon the addition of Al3+ ions to the γ-CD–50 complex [Fig. 12B].
Fig. 12 (A) Salicylaldehyde azine with terminal phenolic –OH (50) forming a strongly fluorescent 1:1 inclusion complexation with γ-CD which acts as a turn-off chemosensor for supramolecular sensing of Al3+ ions; (B) fluorescence microscopy images of 50 in the presence of γ-CD and Al3+ ions displaying a turn-off sensing response (images A and B are adapted with permission from ref. 103. Copyright 2023, Elsevier); (C) syringaldehyde-based azine (51) as a chemosensor for Cu2+ and Pb2+ ions by CHEF and LMCT pathways, respectively; (D) the fluorescence enhancement of 51 with Cu2+ at 413 nm and Pb2+ ions at 473 nm; (E) the 51:β-CD inclusion complex displaying high selectivity towards Al3+ without any interference from Cu2+ and Pb2+; (F) 51:β-CD complex displays a turn-on response against Al3+ addition with an increase in fluorescence intensity at 573 nm; (G) confocal fluorescence imaging indicating fluorescence enhancement with Cu2+ and Pb2+ in the green region and the red emission obtained after the 51:β-CD complex reacts with Al3+ ions (images C–G are adapted with permission from ref. 104. Copyright 2023, Elsevier). |
Narayanan et al. demonstrated a symmetrical azine (51) based on syringaldehyde for the dual detection of metal ions (Cu2+ and Pb2+) in different mechanistic pathways [Fig. 12C].104 The addition of Cu2+ to the azine solution resulted in an enhancement in the emission intensity at 413 nm via the chelation enhanced fluorescence mechanism (CHEF), whereas, in the case of Pb2+ ions, an enhancement in emission intensities with a red-shift to 473 nm was observed due to ligand to metal charge transfer (LMCT) [Fig. 12D]. Interestingly, the inclusion complex of 51 with β-cyclodextrin increases the water solubility and sensing probability and detects Al3+ without any interference from Cu2+ and Pb2+. The high selectivity towards Al3+ may be attributed to the interaction of the hydroxy group of β-CD with the metal ion [Fig. 12E]. The 51:β-CD complex displays a turn-off response which gets drastically changed when Al3+ was added to the supramolecular conjugate and an increase in fluorescence intensity at 573 nm was obtained with a detection limit of 3.2 μM [Fig. 12F]. The fluorescence imaging studies were conducted using confocal microscopy which indicated that the presence of Cu2+ and Pb2+ enhances the green fluorescence and in the case of 51:β-CD + Al3+ a red emission is obtained [Fig. 12G].
Huang et al. demonstrated a salicylaldehyde-based azine polymer with PEG arms (52) [Fig. 13A].107 Due to the hydrophilic PEG segments and hydrophobic salicylaldehyde moieties in the core, the polymer self-assembles into stable micelles in water at ambient temperature and fluoresces orange. Polymer micelles, produced at ambient temperature, can be used as a turn-off fluorescent probe to selectively detect Cu2+ in aqueous environments with a low detection limit of 53 nM. The 52–Cu2+ complex can be employed as a turn-on fluorescent probe for the selective detection of S2− displaying an LOD of 0.24 μM.
Fig. 13 (A) Utilization of salicylaldehyde-based azine for preparation of AIE-polymer 52 and its response towards Cu2+ and S2− ions (image A is adapted with permission from ref. 107. Copyright 2020, Elsevier); (B) and (F) AIE-active polymers 53 and 54 with salicylaldehyde backbones in the main chain via thiol–ene click copolymerization, respectively; (C) fluorescence response of 53 as a function of water content (0 to 8%) showing a decrease in intensity upon addition of water fractions to the amide solvents; (D) decrease in the fluorescence intensity of the supernatant from RBC solutions as a function of hemolysis ratio (0 to 4%); (E) turn-off response displayed by 53 upon addition of Cu2+ ions (images C–E are adapted with permission from ref. 108. Copyright 2021, American Chemical Society). |
Lu and co-workers used thiol–ene click copolymerization of the SA derivative diacrylate monomer, poly(ethylene glycol) diacrylate and 3,6-dioxa-1,8-octanedithiol for the preparation of a multi-functional polymer (53) [Fig. 13B].10853 unexpectedly exhibited intense emission in amide solvents, which gets significantly reduced by the addition of a small amount of water, serving as a water trace indicator in amide solvents [Fig. 13C]. Secondly, the presence of PEG segments facilitated its dispersion in water and the ROS-responsive thioether groups made it a promising scavenger for reactive oxygen species (ROS) [Fig. 13D]. Additionally, the azine moieties served as a fluorescent indicator for hemolysis determination and selective Cu2+ detection owing to the binding capacity of the azine [Fig. 13E]. The same group further demonstrated another amphiphilic AIE-active polymer with dithiothreitol, poly(ethylene glycol) diacrylate, and a salicylaldehyde-based azine (54) with increased water solubility [Fig. 13F].109 PEG segments and DTT units formed stable micelles to help the polymer disseminate in water and preferentially complex with Cu2+, making it a fluorescent sensor in aqueous media.
Wang et al. reported a linear AIE supramolecular polymer (57) from a salicylaldehyde azine-containing pillar[5]arene dimer (55) and an azine-based homoditopic guest (56) and utilized it as a turn-off Cu2+ sensor [Fig. 14].110 The polymer, 57, was strongly fluorescent at high concentration and the addition of Cu2+ ions results in quenching of the fluorescence as the linear supramolecular polymer changes into a cross-linked supramolecular polymer. The fluorescence of the sensor was re-established upon the addition of CN− ions. The cross-linkable AIE supramolecular polymer fabricated by the salicylaldehyde azine-containing pillar[5]arene dimer serves as a promising candidate for advanced materials such as metallogels, sensors, and adaptive coatings.
Fig. 14 Salicylaldehyde azine-containing pillar[5]arene dimer as a supramolecular assembly for detection of Cu2+ and CN− ions (adapted with permission from ref. 110. Copyright 2019, American Chemical Society). |
Farahani et al. utilized a pyridyl-based azine (58) to prepare a Zn-based metal–organic framework that could selectively detect Fe3+ ions in DMF [Fig. 15A].113 The photoinduced electron transfer between the Fe3+ ions and the ligand with the amino-functionalized structure in this MOF is responsible for the effective fluorescence quenching action. In addition, the azine –N donors also contribute their lone-pair electrons to the Fe3+ ions resulting in a notable improvement in the detection capability. With a response time of less than one minute and a detection limit of 0.7 μM, the detection of Fe3+ was highly selective, and there were no interferences from As3+, Cd2+, Zn2+, Co2+, Ni2+, Cu2+, Pb2+, Mn2+, and Al3+ [Fig. 15B].
Fig. 15 (A) Demonstration of a pyridyl-azine (58) for the formation of the cuboidal block Zn-based MOF showing Zn units linked by eight units of 58 and eight units of the amino-1,4-benzenedicarboxylic acid; (B) emission spectra of the Zn-based MOF against various metal ions showing the highest response towards Fe3+ (images A and B are adapted with permission from ref. 113. Copyright 2019, Elsevier); (C) pictorial description of a 3D porous Zn-based luminescent MOF (59); (D) test papers strips coated with 59 showing selective turn-on response towards metal ions such as Cr3+, Al3+ and Fe3+ under 365 nm UV-light (images C and D are adapted with permission from ref. 114. Copyright 2022, American Chemical Society); (E) core structure of the luminescent Cu2+-based MOF (60) with Lewis basic Schiff base sites; (F) % quenching depicted by the Cu-based MOF 60 against different metal ions (image F is adapted with permission from ref. 115. Copyright 2023, Springer). |
Mukherjee et al. developed another substituted pyridyl-based azine probe and used it in the preparation of a highly scalable 3D porous Zn-based MOF 59 by following a mixed ligand synthesis approach [Fig. 15C].114 The aromatic π-conjugated organic linker and N-rich spacer incorporating azine functionality as binding sites for metal ions immobilized within the pore spaces have rendered this MOF an excellent turn-on sensor. A turn-on phenomenon of this nature is uncommon, and a thorough examination indicated an enhancement mechanism attributed to absorbance, known as the absorbance-caused enhancement (ACE) mechanism. It exhibits exceptional sensitivity, selectivity and recyclability for Al3+, Cr3+ and Fe3+ ions. The azine MOF, 59, was further utilized as a simpler, convenient and portable solid-phase detection tool for the sensing of metal ions by turn-on response [Fig. 15D]. The visualization of the MOF 59 loaded silica gel test strips under 365 nm UV-light displayed an enhancement in the fluorescence emission against Cr3+, Al3+ and Fe3+, whereas no change was noted for the other metal ions. In a similar approach, Kaur et al. synthesized a Cu2+-based MOF 60 through the solvothermal method and demonstrated it as a highly selective sensor towards Fe3+ with a low LOD of 47 ppb [Fig. 15E].115 The sensing ability of 60 towards Fe3+ was evaluated against different metal ions and it was noted that no significant quenching was displayed by Ca2+, Ni2+, K+, Pb2+ and Na+ [Fig. 15F]. Ba2+, Cd2+, Zn2+, Co2+, Cu2+ and Al3+ showed a reasonable quenching effect, but the % quenching of 86% shown by Fe3+ ions was the best among the selected metal ions.
Xia et al. synthesized a salicylaldehyde azine-based 2D-COF (61) through the condensation of two non-AIE monomers, 2-hydroxy-1,3,5-triformylbenzene and hydrazine [Fig. 16A].118 The dispersibility and accessibility of the COF were improved by growing the COF in situ on ZIF-90 followed by digestion under mild acidic conditions to form a hollow COF (HOCOF) with a well-designed AIE structure, excellent dispersibility, small size, and low density. The strong red emission of the HOCOF at 635 nm was completely quenched by ammonia (NH3) owing to the break in the hydrogen bonding and unlocking of the rotors of azine segments thereby disabling the AIE modules [Fig. 16B]. The HOCOF displayed a low limit of detection of 157 nM and a broad response range of 0.1–300 μM for the detection of NH3. Further paper-based sensors were demonstrated by soaking disposable filter paper in HOCOF solution and exposing them to NH3. A visual color change from yellow to brownish red was observed in visible light along with a decrease in fluorescence emission under 365 nm UV light [Fig. 16C], indicating the potential of the sensor as an effective and economical strategy for the monitoring of ammonia in industrial production.
Fig. 16 (A) Azine-based emissive COF (61) showing turn off/on reversible response against NH3/HCl. Further utilization of 61 for the hollow COF by the sacrificial template strategy; (B) turn-off fluorescence response displayed by HOCOF with different concentrations of NH3; (C) paper-based HOCOF sensor upon exposure to NH3 for different times (adapted with permission from ref. 118. Copyright 2023, American Chemical Society). |
Fig. 17 (A) and (B) Latent fingerprints of different individuals developed on glass TLC plates and various other surfaces such as aluminium foil, cello tape, currency paper, stainless slide, and marble slate showing the variable scope of latent fingerprinting regardless of the surface under investigation (images A and B are adapted with permission from ref. 120. Copyright 2023, Elsevier); (C) fusion images (transverse, coronal, and sagittal) of dynamic micro-PET/CT study of 63 in APP/PS1 mice and WT mice at different time intervals with the maximum intensity projection (MIP) image at 55–60 min after intravenous administration of 63; (D) fusion images (axial, sagittal, and coronal) of PET/CT study of 63 in the rhesus monkey's head at 0–10 min and 50–60 min post-injection along with the whole-body image at 60–70 min post-injection; (E) PET/CT images after injection in an AD patient and a HC subject showing accumulation of 63 in the cortex while the retention of 63 was mainly in the white matter in the HC subject (images C–E are adapted with permission from ref. 122. Copyright 2023, American Chemical Society). |
The accumulation of β-amyloid (Aβ) in the brain is a pathological biomarker of Alzheimer's disease (AD), manifesting years prior to the appearance of symptoms, and its identification is an integral part of clinical diagnosis.121 Li et al. demonstrated a class of diaryl-azines for detecting Aβ plaques in the AD brain using PET imaging.122 They developed an Aβ-PET tracer, 63, with a high binding affinity to the Aβ aggregates, significant binding ability with the AD brain sections, and optimal brain pharmacokinetic properties in rodents and non-human primates [Fig. 17C and D]. Dynamic PET studies of 63 demonstrated high initial brain uptake in APP/PS1 and WT mice, and subsequent clearance of the radiotracers from the brain was rapid [Fig. 17C]. An in vivo PET study in a rhesus monkey, devoid of Aβ pathology, suggested that 63 efficiently crossed the blood–brain barrier and accumulated in the cortex within 10 min, while rapidly decreasing the radioactivity to the baseline within 50 min [Fig. 17D]. Furthermore, the investigation of the overall body confirmed that no radio-defluorination takes place and 63 was highly stable in primates. The first-in-human PET study declared that 63 displayed low white matter uptake and could bind to Aβ pathology for distinguishing AD from healthy control subjects. The specific signal intensifications of 63 in the AD patient's cortex, especially in the frontal lobe and temporal lobe (common Aβ-burden regions), were confirmed [Fig. 17E]. Interestingly, the cortex of the HC subject did not show any presence of the relevant radioactivity retention and only a few signals were predominantly concentrated in the sub-cortical white matter.
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