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Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions

[Image: see text] Though 1,4-disubstituted 1,2,3-triazole rings have been utilized as electronic bridges in the solution phase, the use of a triazole ring to serve as an electronic bridge of small molecules in the crystalline state has been underdeveloped. Here two compounds with a central 1,4-disub...

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Autores principales: Laird, Rebecca C., Nguyen, Nam P., Rusch, Sara F., Baltrusaitis, Jonas, MacGillivray, Leonard R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983149/
https://www.ncbi.nlm.nih.gov/pubmed/24803847
http://dx.doi.org/10.1021/cg4016542
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author Laird, Rebecca C.
Nguyen, Nam P.
Rusch, Sara F.
Baltrusaitis, Jonas
MacGillivray, Leonard R.
author_facet Laird, Rebecca C.
Nguyen, Nam P.
Rusch, Sara F.
Baltrusaitis, Jonas
MacGillivray, Leonard R.
author_sort Laird, Rebecca C.
collection PubMed
description [Image: see text] Though 1,4-disubstituted 1,2,3-triazole rings have been utilized as electronic bridges in the solution phase, the use of a triazole ring to serve as an electronic bridge of small molecules in the crystalline state has been underdeveloped. Here two compounds with a central 1,4-disubstituted 1,2,3-triazole ring are synthesized to investigate the electronic bridging between terminal stilbazole and pyridine groups in the crystalline phase. The electronic properties of the molecules are characterized through solution phase UV–vis spectroscopy, single crystal X-ray diffractions, and density-of-state and gas-phase DFT calculations. We show that the electronic bridging behavior of a 1,4-disubstituted 1,2,3-triazole ring derived from a click reaction is maintained in the solid state by rare head-to-head (hh) packing in noncentrosymmetric crystal environments.
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spelling pubmed-39831492015-02-17 Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions Laird, Rebecca C. Nguyen, Nam P. Rusch, Sara F. Baltrusaitis, Jonas MacGillivray, Leonard R. Cryst Growth Des [Image: see text] Though 1,4-disubstituted 1,2,3-triazole rings have been utilized as electronic bridges in the solution phase, the use of a triazole ring to serve as an electronic bridge of small molecules in the crystalline state has been underdeveloped. Here two compounds with a central 1,4-disubstituted 1,2,3-triazole ring are synthesized to investigate the electronic bridging between terminal stilbazole and pyridine groups in the crystalline phase. The electronic properties of the molecules are characterized through solution phase UV–vis spectroscopy, single crystal X-ray diffractions, and density-of-state and gas-phase DFT calculations. We show that the electronic bridging behavior of a 1,4-disubstituted 1,2,3-triazole ring derived from a click reaction is maintained in the solid state by rare head-to-head (hh) packing in noncentrosymmetric crystal environments. American Chemical Society 2014-02-17 2014-03-05 /pmc/articles/PMC3983149/ /pubmed/24803847 http://dx.doi.org/10.1021/cg4016542 Text en Copyright © 2014 American Chemical Society
spellingShingle Laird, Rebecca C.
Nguyen, Nam P.
Rusch, Sara F.
Baltrusaitis, Jonas
MacGillivray, Leonard R.
Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title_full Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title_fullStr Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title_full_unstemmed Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title_short Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions
title_sort noncentrosymmetric packings influenced by electronic properties of products of click reactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983149/
https://www.ncbi.nlm.nih.gov/pubmed/24803847
http://dx.doi.org/10.1021/cg4016542
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