Coercing assembly of donor-acceptor complexes with hydrogen-bonded frameworks

被引：4
|
作者：
Yusov, Anna
Dillon, Alexandra M.
Hu, Chunhua T.
Lee, Stephanie S. [1 ]
Ward, Michael D. [1 ]
机构：
[1] New York Univ, Dept Chem, New York, NY 10003 USA
来源：
ORGANIC ELECTRONICS | 2023年 / 115卷
基金：
美国国家科学基金会;
关键词：
Hydrogen bonded frameworks; Tetracyanoquinodimethane; Charge transfer; Solid-state organic materials; Single crystal; Crystallography; CHARGE-TRANSFER; GUEST MOLECULES; TCNQ CRYSTALS; TTF; TETRACYANOQUINODIMETHANE; ELECTROLUMINESCENCE; COCRYSTALS; NETWORKS; SPECTRA; DESIGN;
D O I：
10.1016/j.orgel.2023.106752
中图分类号：
T [工业技术];
学科分类号：
08 ;
摘要：
Guanidinium organosulfonate (GS) hydrogen-bonded frameworks (HBFs) constructed from three different naphthalenesulfonates incorporate the electron acceptor tetracyanoquinodimethane (TCNQ) as a guest molecule, with framework architectures that reflect synergy between the persistent 2D hydrogen-bonded GS network and donor-acceptor interactions. The spectroscopic and computational results confirm weak charge-transfer in-teractions associated with the formation of mixed stacks containing naphthalene donors and TCNQ acceptors that are enforced by the GS framework, suggesting opportunities for the synthesis of new optoelectronic materials through a combination of molecular and crystal design.
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页数：10
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