Issue 9, 2016

Face and edge directed self-assembly of Pd12 tetrahedral nano-cages and their self-sorting

Abstract

Reactions of a cis-blocked Pd(II) 90° acceptor [cis-(tmeda)Pd(NO3)2] (M) with 1,4-di(1H-tetrazol-5-yl)benzene (H2L1) and [1,3,5-tri(1H-tetrazol-5-yl)benzene] (H3L2) in 1 : 1 and 3 : 2 molar ratios respectively, yielded soft metallogels G1 and G2 [tmeda = N,N,N′,N′-tetramethylethane-1,2-diamine]. Post-metalation of the gels G1 and G2 with M yielded highly water-soluble edge and face directed self-assembled Pd12 tetrahedral nano-cages T1 and T2, respectively. Such facile conversion of Pd(II) gels to discrete tetrahedral metallocages is unprecedented. Moreover, distinct self-sorting of these two tetrahedral cages of similar sizes was observed in the self-assembly of M with a mixture of H2L1 and H3L2 in aqueous medium. The edge directed tetrahedral cage (T1) was successfully used to perform Michael reactions of a series of water insoluble nitro-olefins assisted by encapsulation into the cage in aqueous medium.

Graphical abstract: Face and edge directed self-assembly of Pd12 tetrahedral nano-cages and their self-sorting

Associated articles

Supplementary files

Article information

Article type
Edge Article
Submitted
08 May 2016
Accepted
19 May 2016
First published
20 May 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 5893-5899

Face and edge directed self-assembly of Pd12 tetrahedral nano-cages and their self-sorting

P. Howlader and P. S. Mukherjee, Chem. Sci., 2016, 7, 5893 DOI: 10.1039/C6SC02012G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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