TY - JOUR
T1 - Supramolecular Photochirogenesis Driven by Higher-Order Complexation
T2 - Enantiodifferentiating Photocyclodimerization of 2-Anthracenecarboxylate to Slipped Cyclodimers via a 2:2 Complex with β-Cyclodextrin
AU - Wei, Xueqin
AU - Wu, Wanhua
AU - Matsushita, Ryohei
AU - Yan, Zhiqiang
AU - Zhou, Dayang
AU - Chruma, Jason J.
AU - Nishijima, Masaki
AU - Fukuhara, Gaku
AU - Mori, Tadashi
AU - Inoue, Yoshihisa
AU - Yang, Cheng
N1 - Funding Information:
This work was supported by grants from the National Natural Science Foundation of China (21572142, 21372165, 21321061, and 21402129) and the National Key Research and Development Program of China (2017YFA0505900) to C.Y. and also by Grants-in-Aid for Scientific Research, Challenging Exploratory Research, Promotion of Joint International Research (Fostering Joint International Research), and Innovative Area “Photosynergetics” (JP15H03779, JP15K13642, JP16KK0111, and JP17H05261) from the Japan Society for the Promotion of Science, Asahi Glass Foundation, and Cosmetology Research Foundation to T.M., all of which are gratefully acknowledged. C.Y. is grateful to Prof. Peng Wu and Huiqin Sun for the analyses at the Analytical and Testing Center of Sichuan University.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/3/21
Y1 - 2018/3/21
N2 - Chiral slipped 5,8:9′,10′-cyclodimers were preferentially produced over classical 9,10:9′,10′-cyclodimers upon supramolecular photocyclodimerization of 2-anthracenecarboxylate (AC) mediated by β-cyclodextrin (β-CD). This photochirogenic route to the slipped cyclodimers, exclusively head-to-tail (HT) and highly enantioselective, has long been overlooked in foregoing studies but is dominant in reality and is absolutely supramolecularly activated by 2:2 complexation of AC with β-CD. The intricate structural and photophysical aspects of this higher-order complexation-triggered process have been comprehensively elucidated, while the absolute configurations of the slipped cyclodimers have been unambiguously assigned by comparing the experimental and theoretical circular dichroism spectra. In the 2:2 complex, two ACs packed in a dual β-CD capsule are not fully overlapped with each other but are only partially stacked in a slipped anti- or syn-HT manner. Hence, they do not spontaneously cyclodimerize upon photoexcitation but instead emit long-lived excimer fluorescence at wavelengths slightly longer than the monomer fluorescence, indicating that the slipped excimer is neither extremely reactive nor completely relaxed in conformation and energy. Because of the slipped conformation of the AC pair in the soft capsule, the subsequent photocyclodimerization becomes manipulable by various internal or external factors, such as temperature, pressure, added salt, and host modification, enabling us to exclusively obtain the slipped cyclodimers with high regio- and enantioselectivities. In this supramolecularly driven photochirogenesis, the dual β-CD capsule functions as a chiral organophotocatalyst to trigger and accelerate the nonclassical photochirogenic route to slipped cyclodimers by preorganizing the conformation of the encapsulated AC pair, formally mimicking a catalytic antibody.
AB - Chiral slipped 5,8:9′,10′-cyclodimers were preferentially produced over classical 9,10:9′,10′-cyclodimers upon supramolecular photocyclodimerization of 2-anthracenecarboxylate (AC) mediated by β-cyclodextrin (β-CD). This photochirogenic route to the slipped cyclodimers, exclusively head-to-tail (HT) and highly enantioselective, has long been overlooked in foregoing studies but is dominant in reality and is absolutely supramolecularly activated by 2:2 complexation of AC with β-CD. The intricate structural and photophysical aspects of this higher-order complexation-triggered process have been comprehensively elucidated, while the absolute configurations of the slipped cyclodimers have been unambiguously assigned by comparing the experimental and theoretical circular dichroism spectra. In the 2:2 complex, two ACs packed in a dual β-CD capsule are not fully overlapped with each other but are only partially stacked in a slipped anti- or syn-HT manner. Hence, they do not spontaneously cyclodimerize upon photoexcitation but instead emit long-lived excimer fluorescence at wavelengths slightly longer than the monomer fluorescence, indicating that the slipped excimer is neither extremely reactive nor completely relaxed in conformation and energy. Because of the slipped conformation of the AC pair in the soft capsule, the subsequent photocyclodimerization becomes manipulable by various internal or external factors, such as temperature, pressure, added salt, and host modification, enabling us to exclusively obtain the slipped cyclodimers with high regio- and enantioselectivities. In this supramolecularly driven photochirogenesis, the dual β-CD capsule functions as a chiral organophotocatalyst to trigger and accelerate the nonclassical photochirogenic route to slipped cyclodimers by preorganizing the conformation of the encapsulated AC pair, formally mimicking a catalytic antibody.
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U2 - 10.1021/jacs.7b12085
DO - 10.1021/jacs.7b12085
M3 - Article
C2 - 29437396
AN - SCOPUS:85044396805
SN - 0002-7863
VL - 140
SP - 3959
EP - 3974
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 11
ER -