Noncovalent interactions colorize aggregate photophysics

被引：2
|
作者：
Zhang, Jianyu [1 ]
Zhang, Haoke [2 ,3 ]
Tang, Ben Zhong [1 ,4 ,5 ]
机构：
[1] Hong Kong Univ Sci & Technol, Chinese Natl Engn Res Ctr Tissue Restorat & Recons, Dept Chem, Hong Kong Branch,Kowloon, Clear Water Bay, Hong Kong 999077, Peoples R China
[2] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, ZJU Hangzhou Global Sci & Technol Innovat Ctr, Zhejiang Israel Joint Lab Selfassembling Funct Mat, Hangzhou 311215, Zhejiang, Peoples R China
[4] Zhejiang Univ, Shaoxing Inst, Ctr Healthcare Mat, Shaoxing 312000, Peoples R China
[5] Chinese Univ Hong Kong, Shenzhen Inst Aggregate Sci & Technol, Sch Sci & Engn, Shenzhen 518172, Guangdong, Peoples R China
来源：
MATTER | 2023年 / 6卷 / 11期
基金：
中国国家自然科学基金;
关键词：
INDUCED EMISSION; THROUGH-SPACE;
D O I：
10.1016/j.matt.2023.10.005
中图分类号：
T [工业技术];
学科分类号：
08 ;
摘要：
Noncovalent interactions play an increasingly essential role in manipulating the photophysical properties of poorly conjugated lu-minogens, especially in the aggregate and solid states. In a recent study published in the Journal of the American Chemical Society, McGonigal, Jones, Moggach, and co-workers provide solid struc-ture-property evidence on how subtle structural changes and non-covalent interactions colorize the photophysical properties of fluo-rescent organic molecular rotors under high pressure.
引用
收藏
页码：3702 / 3704
页数：3
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