Abstract

Spin–spin interactions between two identical aromatic radicals have been studied extensively and utilized to establish supramolecular recognition. Here we report that spin-pairing interactions could also take place between two different π-electron radicals, namely a bipyridinium radical cation (BPY+•) and a naphthalene-1,8:4,5-bis(dicarboximide) radical anion (NDI─•). The occurrence of this type of previously unreported hetero radical-pairing interactions is attributed to enhancement effect of Coulombic attraction between these two radicals bearing opposite charges. The Coulombic-enhanced hetero radical pairing interactions are employed to drive host–guest recognition, as well as the reversible switching of a bistable [2]rotaxane.

Details

Title
Coulombic-enhanced hetero radical pairing interactions
Author
Zheng, Xujun 1 ; Zhang, Yang 2 ; Cao, Ning 2 ; Li, Xin 2 ; Zhang, Shuoqing 2 ; Du, Renfeng 2 ; Wang, Haiying 3 ; Ye, Zhenni 2 ; Wang, Yan 2 ; Cao, Fahe 2   VIAFID ORCID Logo  ; Li, Haoran 2 ; Hong, Xin 2   VIAFID ORCID Logo  ; Sue, Andrew C-H 3 ; Yang, Chuluo 4 ; Wei-Guang Liu 5 ; Li, Hao 2   VIAFID ORCID Logo 

 Department of Chemistry, Zhejiang University, Hangzhou, China; Department of Chemistry, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, Wuhan University, Wuhan, China 
 Department of Chemistry, Zhejiang University, Hangzhou, China 
 Institute for Molecular Design and Synthesis, School of Pharmaceutical Science & Technology, Health Science Platform, Tianjin University, Tianjin, China 
 Department of Chemistry, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, Wuhan University, Wuhan, China 
 Department of Chemistry, Chemical Theory Center, and Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN, USA 
Pages
1-9
Publication year
2018
Publication date
May 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2040740625
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.