Affiliation:
1. School of Materials Science and Engineering University of Science and Technology Beijing Beijing 100083 China
2. School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing 100083 China
Abstract
AbstractThe construction of tunable morphological systems has important implications for understanding the mechanism of molecular self‐assembly. In this study, a spiropyran derivative M1 is reported with light‐responsive assembly morphology, which can be tuned from nanosphere to nanorod by ultraviolet light irradiation. The absorption spectra show that M1 molecules are transformed from closed‐ring (SP) isomers into open‐ring (MC) isomers and start to form H‐aggregates with increasing irradiation time. Density functional theory calculations indicate that MC‐MC isomers possess stronger binding energy than SP‐SP isomers. The MC isomers may thus facilitate the dissociation of the SP‐SP aggregates and promote the change of self‐assembled morphology with the aid of stronger π‐π stackings and dipole‐dipole interactions. The research gives an effective method for modulating the morphology of assemblies, with great potential for applications in smart materials.
Funder
Fundamental Research Funds for the Central Universities
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Program for New Century Excellent Talents in University
Subject
Materials Chemistry,Polymers and Plastics,Organic Chemistry
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献