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基于二蒽基硼的供体-受体体系的设计、合成及温度驱动的分子构象依赖性延迟荧光特性

Design, Synthesis, and Temperature-Driven Molecular Conformation-Dependent Delayed Fluorescence Characteristics of Dianthrylboron-Based Donor-Acceptor Systems.

作者信息

Pandey Umesh Pratap, Nandi Rajendra Prasad, Thilagar Pakkirisamy

机构信息

Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, India.

出版信息

Front Chem. 2020 Oct 9;8:541331. doi: 10.3389/fchem.2020.541331. eCollection 2020.

DOI:10.3389/fchem.2020.541331
PMID:33195044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7581868/
Abstract

We report a simple and novel molecular design strategy to enhance rISC in boron-based donor-acceptor systems to achieve improved delayed fluorescence characteristics. Dianthrylboryl ((An)B)-based aryl aminoboranes (donor: phenothiazine) and (donor: N,N-diphenylamine) were synthesized by a simple one-pot procedure. The energy of the electronic excited states in and were modulated by varying the arylamine donor strength and electronic coupling between D and A moieties. The presence of a large π-system (anthryl moiety) on boron enhances the electronic communication between donor arylamine and acceptor boryl moieties, and hence, both and exhibit delayed fluorescence characteristics in a broad range of temperatures (80-300 K). Single crystal X-ray analysis and temperature-dependent photophysical studies together with theoretical studies were carried out to rationalize the observed intriguing optical signatures of and .

摘要

我们报道了一种简单且新颖的分子设计策略,用于增强基于硼的供体 - 受体体系中的室温磷光,以实现改善的延迟荧光特性。通过简单的一锅法合成了基于二蒽基硼基((An)B)的芳基氨基硼烷(供体:吩噻嗪)和(供体:N,N - 二苯胺)。通过改变芳胺供体强度以及 D 和 A 部分之间的电子耦合,调节了 和 中电子激发态的能量。硼上大 π 体系(蒽基部分)的存在增强了供体芳胺和受体硼基部分之间的电子通信,因此, 和 在很宽的温度范围(80 - 300 K)内都表现出延迟荧光特性。进行了单晶 X 射线分析、温度依赖的光物理研究以及理论研究,以合理解释观察到的 和 有趣的光学特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/a4db564d73b2/fchem-08-541331-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/b1a1a6421c30/fchem-08-541331-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/f0cc5b165cab/fchem-08-541331-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/d74e9d2c736c/fchem-08-541331-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/c8132abe2dfa/fchem-08-541331-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/b8a7582d2ae7/fchem-08-541331-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/8528dbef1be0/fchem-08-541331-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/a4db564d73b2/fchem-08-541331-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/b1a1a6421c30/fchem-08-541331-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/f0cc5b165cab/fchem-08-541331-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/b3cd26b528ba/fchem-08-541331-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/e0756aec3253/fchem-08-541331-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/d74e9d2c736c/fchem-08-541331-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/c8132abe2dfa/fchem-08-541331-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/b8a7582d2ae7/fchem-08-541331-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/8528dbef1be0/fchem-08-541331-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ab/7581868/a4db564d73b2/fchem-08-541331-g0008.jpg

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