Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylate mediated by a self-assembled iron tetrahedral coordination cage
[Display omitted] •An enantiopure molecular cage was used for mediating a chiral photodimerization.•The intrinsically chiral cage demonstrated efficiency in the chiral induction.•External factors play a remarkable role in the supramolecular photochirogenesis. Photochirogenesis through supramolecular...
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Published in | Journal of photochemistry and photobiology. A, Chemistry. Vol. 331; pp. 95 - 101 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
01.12.2016
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Abstract | [Display omitted]
•An enantiopure molecular cage was used for mediating a chiral photodimerization.•The intrinsically chiral cage demonstrated efficiency in the chiral induction.•External factors play a remarkable role in the supramolecular photochirogenesis.
Photochirogenesis through supramolecular assembly provides an intriguing approach to the highly challenging research field of chiral photochemistry. In the present paper, an enantiopure coordination self-assembly cage (cage T) has been employed for mediating the enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylate (AC) in aqueous medium. The complexing behavior of AC with the cage T has been investigated by UV–vis, circular dichroism and NMR spectral studies. It was found that in aqueous solution, cage T could form both 1:1 and 1:2 host–guest complexes with AC. Photocyclodimerization of AC mediated by cage T were studied at different temperatures and different host/guest ratios. The anti-HT photodimer dominate the photocyclodimerization of AC with cage T. In the presence of an enantiopure cage T, the chiral syn-HT and anti-HH photodimers were produced in moderate enantioselectivity. The enantiodifferentiating mechanism of this supramolecular photochirogenesis system and the effects of external factors are discussed. |
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AbstractList | [Display omitted]
•An enantiopure molecular cage was used for mediating a chiral photodimerization.•The intrinsically chiral cage demonstrated efficiency in the chiral induction.•External factors play a remarkable role in the supramolecular photochirogenesis.
Photochirogenesis through supramolecular assembly provides an intriguing approach to the highly challenging research field of chiral photochemistry. In the present paper, an enantiopure coordination self-assembly cage (cage T) has been employed for mediating the enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylate (AC) in aqueous medium. The complexing behavior of AC with the cage T has been investigated by UV–vis, circular dichroism and NMR spectral studies. It was found that in aqueous solution, cage T could form both 1:1 and 1:2 host–guest complexes with AC. Photocyclodimerization of AC mediated by cage T were studied at different temperatures and different host/guest ratios. The anti-HT photodimer dominate the photocyclodimerization of AC with cage T. In the presence of an enantiopure cage T, the chiral syn-HT and anti-HH photodimers were produced in moderate enantioselectivity. The enantiodifferentiating mechanism of this supramolecular photochirogenesis system and the effects of external factors are discussed. Photochirogenesis through supramolecular assembly provides an intriguing approach to the highly challenging research field of chiral photochemistry. In the present paper, an enantiopure coordination self-assembly cage (cage T) has been employed for mediating the enantiodifferentiating [4 + 4] photocyclodimerization of 2-anthracenecarboxylate (AC) in aqueous medium. The complexing behavior of AC with the cage T has been investigated by UV-vis, circular dichroism and NMR spectral studies. It was found that in aqueous solution, cage T could form both 1:1 and 1:2 host-guest complexes with AC. Photocyclodimerization of AC mediated by cage T were studied at different temperatures and different host/guest ratios. The anti-HT photodimer dominate the photocyclodimerization of AC with cage T. In the presence of an enantiopure cage T, the chiral syn-HT and anti-HH photodimers were produced in moderate enantioselectivity. The enantiodifferentiating mechanism of this supramolecular photochirogenesis system and the effects of external factors are discussed. |
Author | Yang, Cheng Alagesan, Mani Zhang, Hui Sun, Huiqin Wu, Wanhua Gao, Guowei Zhong, Zhihui Zhou, Dayang Kanagaraj, Kuppusamy Wan, Shigang Su, Dan |
Author_xml | – sequence: 1 givenname: Mani surname: Alagesan fullname: Alagesan, Mani organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 2 givenname: Kuppusamy surname: Kanagaraj fullname: Kanagaraj, Kuppusamy organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 3 givenname: Shigang surname: Wan fullname: Wan, Shigang organization: Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China – sequence: 4 givenname: Huiqin surname: Sun fullname: Sun, Huiqin organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 5 givenname: Dan surname: Su fullname: Su, Dan organization: State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, PR China – sequence: 6 givenname: Zhihui surname: Zhong fullname: Zhong, Zhihui organization: State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, PR China – sequence: 7 givenname: Dayang surname: Zhou fullname: Zhou, Dayang organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 8 givenname: Wanhua surname: Wu fullname: Wu, Wanhua organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 9 givenname: Guowei surname: Gao fullname: Gao, Guowei organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China – sequence: 10 givenname: Hui surname: Zhang fullname: Zhang, Hui email: huizhang@xmu.edu.cn organization: Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China – sequence: 11 givenname: Cheng surname: Yang fullname: Yang, Cheng email: yangchengyc@scu.edu.cn organization: Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, PR China |
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Keywords | Temperature effect Photocyclodimerization Anthracene Cooordination cage Chirality |
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•An enantiopure molecular cage was used for mediating a chiral photodimerization.•The intrinsically chiral cage demonstrated efficiency in... Photochirogenesis through supramolecular assembly provides an intriguing approach to the highly challenging research field of chiral photochemistry. In the... |
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SubjectTerms | Anthracene Cages Chirality Circular dichroism Cooordination cage Dichroism Enantiomers Iron Molecular chemistry NMR Nuclear magnetic resonance Photochemistry Photocyclodimerization Self-assembly Studies Supramolecular compounds Temperature effect Temperature effects |
Title | Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylate mediated by a self-assembled iron tetrahedral coordination cage |
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