Mixed-stack architecture and solvatomorphism of trimeric perfluoro-ortho-phenylene mercury complexes with dithieno[3,2-b:2′,3′-d] thiophene

被引:7
作者
Castaneda, Raul [1 ]
Khrustalev, Victor N. [1 ,2 ]
Fonari, Alexandr [3 ,4 ]
Bredas, Jean-Luc [5 ,6 ]
Getmanenko, Yulia A. [1 ,3 ,4 ]
Timofeeva, Tatiana V. [1 ,7 ]
机构
[1] New Mexico Highlands Univ, Dept Chem & Biol, Las Vegas, NM 87701 USA
[2] Peoples Friendship Univ Russia, Moscow 117198, Russia
[3] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[4] Georgia Inst Technol, Ctr Organ Photon & Elect, Atlanta, GA 30332 USA
[5] King Abdullah Univ Sci & Technol, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia
[6] King Abdullah Univ Sci & Technol, Solar & Photovolta Engn Res Ctr, Thuwal 239556900, Saudi Arabia
[7] ITMO Univ, Dept Engn Photon, St Petersburg 197101, Russia
基金
美国国家科学基金会;
关键词
Dithieno[3,2-b:2',3'-d]thiophene; Trimeric perfluoro-ortho-phenylene mercury; Secondary interactions; Solvatomorphism; X-ray diffraction; Quantum chemistry; THIN-FILM TRANSISTORS; CHARGE-TRANSFER CRYSTALS; FIELD-EFFECT TRANSISTORS; CO-CRYSTAL; SEMICONDUCTOR; DERIVATIVES; POLYMER; ACCEPTOR; OLIGOTHIOPHENES; LUMINESCENT;
D O I
10.1016/j.molstruc.2015.07.053
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The formation of the mixed-stack donor acceptor complex of dithieno [3,2-b:2',3'-d]thiophene (1) and trimeric perfluoro-ortho-phenylene mercury (I) has been investigated under different conditions. Two solvatomorphs mixed-stack complexes with a 1:1 donor acceptor ratio and different solvent molecules in the solid state (dichloromethane (2) and dichloroethane (3)) have been obtained and characterized by experimental methods (Fr-IR spectroscopy, differential thermogravimetric analysis, and X-ray crystallography) and quantum-chemical calculations at the density functional theory level. The differences in the solid state packing, thermal stability and potential charge-transfer properties of 2 and 3 are discussed. (C) 2015 Elsevier B.V. All rights reserved,
引用
收藏
页码:506 / 512
页数:7
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