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Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties

A single crystal of pyrenylsumanene was found to exhibit both columnar and herringbone crystal packing. The sumanene moieties form unidirectional columnar structures based on π–π stacking while the pyrene moieties generate herringbone structures due to CH–π interactions. The absorption and emission...

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Autores principales: Shrestha, Binod Babu, Higashibayashi, Shuhei, Sakurai, Hidehiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999760/
https://www.ncbi.nlm.nih.gov/pubmed/24778739
http://dx.doi.org/10.3762/bjoc.10.80
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author Shrestha, Binod Babu
Higashibayashi, Shuhei
Sakurai, Hidehiro
author_facet Shrestha, Binod Babu
Higashibayashi, Shuhei
Sakurai, Hidehiro
author_sort Shrestha, Binod Babu
collection PubMed
description A single crystal of pyrenylsumanene was found to exhibit both columnar and herringbone crystal packing. The sumanene moieties form unidirectional columnar structures based on π–π stacking while the pyrene moieties generate herringbone structures due to CH–π interactions. The absorption and emission maxima of pyrenylsumanene were both red-shifted relative to those of sumanene and pyrene, owing to the extension of π-conjugation. Monomer emission with high quantum yield (0.82) was observed for pyrenylsumanene in solution, while excimer-type red-shifted emission was evident in the crystalline phase.
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spelling pubmed-39997602014-04-28 Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties Shrestha, Binod Babu Higashibayashi, Shuhei Sakurai, Hidehiro Beilstein J Org Chem Full Research Paper A single crystal of pyrenylsumanene was found to exhibit both columnar and herringbone crystal packing. The sumanene moieties form unidirectional columnar structures based on π–π stacking while the pyrene moieties generate herringbone structures due to CH–π interactions. The absorption and emission maxima of pyrenylsumanene were both red-shifted relative to those of sumanene and pyrene, owing to the extension of π-conjugation. Monomer emission with high quantum yield (0.82) was observed for pyrenylsumanene in solution, while excimer-type red-shifted emission was evident in the crystalline phase. Beilstein-Institut 2014-04-11 /pmc/articles/PMC3999760/ /pubmed/24778739 http://dx.doi.org/10.3762/bjoc.10.80 Text en Copyright © 2014, Shrestha 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
Shrestha, Binod Babu
Higashibayashi, Shuhei
Sakurai, Hidehiro
Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title_full Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title_fullStr Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title_full_unstemmed Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title_short Columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
title_sort columnar/herringbone dual crystal packing of pyrenylsumanene and its photophysical properties
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999760/
https://www.ncbi.nlm.nih.gov/pubmed/24778739
http://dx.doi.org/10.3762/bjoc.10.80
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