pH-Controlled enantioselectivity switching of irregular photodimers in photocyclodimerization of 2-anthracenecarboxylic acid mediated with β-cyclodextrin derivatives-Reference-Cited by-同舟云学术

pH-Controlled enantioselectivity switching of irregular photodimers in photocyclodimerization of 2-anthracenecarboxylic acid mediated with β-cyclodextrin derivatives

Published:2022 Issue:48 Volume:46 Page:23066-23076
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kanagaraj Kuppusamy¹²^ORCID,Ji Jiecheng¹,Rao Ming¹,Fan Chunying¹,Xiao Chao¹,Zhou Dayang³,Wu Wanhua¹^ORCID,Selvapalam Narayanan⁴,Yu Yang²^ORCID,Yang Cheng¹^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu, 610064, China

2. Center for Supramolecular Chemistry & Catalysis and Department of Chemistry, College of Science, Shanghai University, Shanghai, 200444, China

3. Comprehensive Analysis Center, ISIR, Osaka University, Japan

4. Department of Chemistry, Kalasalingam University, India

Abstract

β-CDx derivatives invert the stereochemical outcome of syn-head-to-tail-photodimers, upon changing solution pH, solving the problem of antipodal-chiral hosts not being available.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Department of Science and Technology of Sichuan Province

Fundamental Research Funds for the Central Universities

Sichuan University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ03940K