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Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes

A series of donor–acceptor type co-crystals of fullerene (as the acceptor) and arylthio-substituted tetrathiafulvalene derivatives (Ar-S-TTF, as the donor) were prepared and their structural features were thoroughly investigated. The formation of co-crystals relies on the flexibility of Ar-S-TTF and...

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Autores principales: Lu, Xiaofeng, Sun, Jibin, Zhang, Shangxi, Ma, Longfei, Liu, Lei, Qi, Hui, Shao, Yongliang, Shao, Xiangfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505149/
https://www.ncbi.nlm.nih.gov/pubmed/26199659
http://dx.doi.org/10.3762/bjoc.11.117
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author Lu, Xiaofeng
Sun, Jibin
Zhang, Shangxi
Ma, Longfei
Liu, Lei
Qi, Hui
Shao, Yongliang
Shao, Xiangfeng
author_facet Lu, Xiaofeng
Sun, Jibin
Zhang, Shangxi
Ma, Longfei
Liu, Lei
Qi, Hui
Shao, Yongliang
Shao, Xiangfeng
author_sort Lu, Xiaofeng
collection PubMed
description A series of donor–acceptor type co-crystals of fullerene (as the acceptor) and arylthio-substituted tetrathiafulvalene derivatives (Ar-S-TTF, as the donor) were prepared and their structural features were thoroughly investigated. The formation of co-crystals relies on the flexibility of Ar-S-TTF and the size matches between Ar-S-TTF and fullerene. Regarding their compositions, the studied co-crystals can be divided into two types, where types I and II have donor:acceptor ratios of 1:1 and 1:2, respectively. Multiple intermolecular interactions are observed between the donor and acceptor, which act to stabilize the structures of the resulting co-crystals. In the type I co-crystals, the fullerene molecule is surrounded by four Ar-S-TTF molecules, that is, two Ar-S-TTF molecules form a sandwich structure with one fullerene molecule and the other two Ar-S-TTF molecules interact with the fullerene molecule along their lateral axes. In the type II co-crystals, one fullerene molecule has the donor–acceptor mode similar to that in type I, whereas the other fullerene molecule is substantially surrounded by the aryl groups on Ar-S-TTF molecules and the solvent molecules.
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spelling pubmed-45051492015-07-21 Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes Lu, Xiaofeng Sun, Jibin Zhang, Shangxi Ma, Longfei Liu, Lei Qi, Hui Shao, Yongliang Shao, Xiangfeng Beilstein J Org Chem Full Research Paper A series of donor–acceptor type co-crystals of fullerene (as the acceptor) and arylthio-substituted tetrathiafulvalene derivatives (Ar-S-TTF, as the donor) were prepared and their structural features were thoroughly investigated. The formation of co-crystals relies on the flexibility of Ar-S-TTF and the size matches between Ar-S-TTF and fullerene. Regarding their compositions, the studied co-crystals can be divided into two types, where types I and II have donor:acceptor ratios of 1:1 and 1:2, respectively. Multiple intermolecular interactions are observed between the donor and acceptor, which act to stabilize the structures of the resulting co-crystals. In the type I co-crystals, the fullerene molecule is surrounded by four Ar-S-TTF molecules, that is, two Ar-S-TTF molecules form a sandwich structure with one fullerene molecule and the other two Ar-S-TTF molecules interact with the fullerene molecule along their lateral axes. In the type II co-crystals, one fullerene molecule has the donor–acceptor mode similar to that in type I, whereas the other fullerene molecule is substantially surrounded by the aryl groups on Ar-S-TTF molecules and the solvent molecules. Beilstein-Institut 2015-06-19 /pmc/articles/PMC4505149/ /pubmed/26199659 http://dx.doi.org/10.3762/bjoc.11.117 Text en Copyright © 2015, Lu et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Lu, Xiaofeng
Sun, Jibin
Zhang, Shangxi
Ma, Longfei
Liu, Lei
Qi, Hui
Shao, Yongliang
Shao, Xiangfeng
Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title_full Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title_fullStr Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title_full_unstemmed Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title_short Donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
title_sort donor–acceptor type co-crystals of arylthio-substituted tetrathiafulvalenes and fullerenes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505149/
https://www.ncbi.nlm.nih.gov/pubmed/26199659
http://dx.doi.org/10.3762/bjoc.11.117
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