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Supramolecular photochirogenesis in sensitizing chiral nanopore: Enantiodifferentiating photoisomerization of (Z)-cyclooctene included and sensitized by POST-1 SCIE SCOPUS

Title
Supramolecular photochirogenesis in sensitizing chiral nanopore: Enantiodifferentiating photoisomerization of (Z)-cyclooctene included and sensitized by POST-1
Authors
Gao, YWada, TYang, KKim, KInoue, Y
Date Issued
2005-01
Publisher
WILEY-LISS
Abstract
By using homochiral mesoporous POST-1 (Scheme 1) as an inherently chiral sensitizing host, supramolecular enantiodifferentiating photoisomerizations of (Z)-cyclooctene (1Z) were performed for the first time to examine the sensitizing ability of the chiral nanopores, walls of which are decorated with pyridine chromophore. The homochiral nanopores of POST-1 crystals were demonstrated to function as an effective chiral-sensitizing cavity to give the optically active (E)-isomer 1E in up to 5% enantiomeric excess (ee), thus expanding the scope of porous material-mediated chirogenesis to both ground and excited electronic states. Chirality 17:S19-S23, 2005. (c) 2005 Wiley-Liss, Inc.
Keywords
asymmetric synthesis; chiral photochemistry; homochiral material; photosensitization; sensitizing host; metal-organic porous materials; ASYMMETRIC PHOTOCHEMISTRY; PRODUCT CHIRALITY; CYCLOOCTENE; ISOMERIZATION; TEMPERATURE; BENZENEPOLYCARBOXYLATES
URI
https://oasis.postech.ac.kr/handle/2014.oak/24504
DOI
10.1002/CHIR.20102
ISSN
0899-0042
Article Type
Article
Citation
CHIRALITY, vol. 17, page. S19 - S23, 2005-01
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김기문KIM, KIMOON
Dept of Chemistry
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