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Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile

The title organic compound, C(37)H(23)N, crystallizing in the triclinic space group P [Image: see text], has been designed, synthesized and characterized by single-crystal X-ray diffaction, MS, NMR and elemental analysis. There are alternating relatively strong and weak intermolecular π–π interactio...

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Detalles Bibliográficos
Autores principales: Miao, Bao-Xi, Tang, Xin-Xue, Zhang, Li-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947477/
https://www.ncbi.nlm.nih.gov/pubmed/29850081
http://dx.doi.org/10.1107/S2056989018005182
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author Miao, Bao-Xi
Tang, Xin-Xue
Zhang, Li-Fang
author_facet Miao, Bao-Xi
Tang, Xin-Xue
Zhang, Li-Fang
author_sort Miao, Bao-Xi
collection PubMed
description The title organic compound, C(37)H(23)N, crystallizing in the triclinic space group P [Image: see text], has been designed, synthesized and characterized by single-crystal X-ray diffaction, MS, NMR and elemental analysis. There are alternating relatively strong and weak intermolecular π–π interactions between adjacent pyrene ring systems, forming a one-dimensional supramolecular structure. The compound is weakly fluorescent in THF solution, but it is highly emissive in the condensed phase, revealing distinct aggregation-induced emission (AIE) characteristics.
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spelling pubmed-59474772018-05-30 Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile Miao, Bao-Xi Tang, Xin-Xue Zhang, Li-Fang Acta Crystallogr E Crystallogr Commun Research Communications The title organic compound, C(37)H(23)N, crystallizing in the triclinic space group P [Image: see text], has been designed, synthesized and characterized by single-crystal X-ray diffaction, MS, NMR and elemental analysis. There are alternating relatively strong and weak intermolecular π–π interactions between adjacent pyrene ring systems, forming a one-dimensional supramolecular structure. The compound is weakly fluorescent in THF solution, but it is highly emissive in the condensed phase, revealing distinct aggregation-induced emission (AIE) characteristics. International Union of Crystallography 2018-04-06 /pmc/articles/PMC5947477/ /pubmed/29850081 http://dx.doi.org/10.1107/S2056989018005182 Text en © Miao et al. 2018 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/
spellingShingle Research Communications
Miao, Bao-Xi
Tang, Xin-Xue
Zhang, Li-Fang
Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title_full Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title_fullStr Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title_full_unstemmed Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title_short Synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
title_sort synthesis, crystal structure and aggregation-induced emission of a new pyrene-based compound, 3,3-diphenyl-2-[4-(pyren-1-yl)phen­yl]acrylo­nitrile
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947477/
https://www.ncbi.nlm.nih.gov/pubmed/29850081
http://dx.doi.org/10.1107/S2056989018005182
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