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Fascinating chiral information transfer to titania/silica from near to racemic compound self-organized from polyethyleneimine and tartaric acid.

作者信息

Oota Kei, Jin Ren-Hua

机构信息

Department of Material and Life Chemistry, Kanagawa University, 3-27-1 Rokkakubashi, Yokohama 221-8686, Japan.

出版信息

Dalton Trans. 2023 Jul 25;52(29):9913-9928. doi: 10.1039/d3dt00652b.

DOI:10.1039/d3dt00652b
PMID:37401862
Abstract

In this work, chiroptical crystalline complexes of PEI/Tart (P/T) consisting of linear poly(ethylemeimine) (PEI) and an enantiomeric excess (ee) of tartaric acid (Tart) were used as chiral catalytic templates in the hydrolytic condensation of titanium bislactates and co-condensation of titanium bislactates and tetramethoxysilane for the preparation of chiral titania (TiO) and chiral titania/silica (TiO/SiO) hybrid. Different from the general case of enantiopure templates excelling in chiral transformation when compared to enantiomeric excess ones, P/T systems with different enantiomer ratios exhibited each activity in the transformation of their chiral information to the resulting minerals titania and titania/silica. Especially, the P/T complexes with ee only by ±4% (D/L = 52/48 or 48/52), which is near the racemic state (D/L = 50/50), served as excellent chiral catalytic templates to generate chiroptical titania and titania/silica with mirror relation of the CD signals. By means of DSC, XRD, SEM and DRCD techniques, the crystalline complexes of PEI/Tart (P/T), the as-prepared TiO@P/T and TiO/SiO@P/T, and the calcined TiO and TiO/SiO were thoroughly investigated and the mechanism of the chiral transformation from the enantiomeric excess of P/T to minerals was proposed.

摘要

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