Wei
He
,
Shohei
Tashiro
* and
Mitsuhiko
Shionoya
*
Department of Chemistry, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan. E-mail: shionoya@chem.s.u-tokyo.ac.jp
First published on 11th August 2022
Correction for ‘Highly selective acid-catalyzed olefin isomerization of limonene to terpinolene by kinetic suppression of overreactions in a confined space of porous metal–macrocycle frameworks’ by Wei He et al., Chem. Sci., 2022, 13, 8752–8758, https://doi.org/10.1039/d2sc01561g.
Fig. 2 Metal–macrocycle framework (MMF). (a) Self-assembly of asymmetrically twisted PdII-macrocycles into (b) a porous crystal MMF (sticks model) with five enantiomeric pairs of binding pockets (surface model). (c) Previously reported site-selective adsorption of (−)-α-pinene (6) (space-filling model) on the channel surface of the MMF.1 Blue, yellow, red, or black dashed circles indicate the ceiling-, side-, bottom-, or tubular-pockets of the MMF, respectively. MMF: Pd, yellow; Cl, green; N, blue; C, grey. 6: C, pink; H, white. Hydrogen atoms attached to the MMF were omitted for clarity. Green or blue surface represents exposed Cl or N–H groups of the MMF, respectively. |
Fig. 5 Investigation of the inhibitory effects of additives on the isomerization reaction of 2 using 2-NBSA@MMF at 25 °C for 102 h. |
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