Diarylpyrenes vs. diaryltetrahydropyrenes

The synthesis of two series of substituted 2,7-diaryl-4,5,9,10-tetrahydropyrenes (1a–c) and 2,7-diarylpyrenes (2a–c) is reported; the opposing phenyl tips being terminated with tBu (a), OCH3 (b), or F (c) to impart variation in electronic properties. X-ray crystallographic analysis of the six compou...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: El-Ballouli, Alaa O. (author)
مؤلفون آخرون: Khnayzer, Rony S. (author), Khalife, Jihane C. (author), Fonari, Alexandr (author), Hallal, Kassem M. (author), Timofeeva, Tatiana V. (author), Digambara, Patra (author), Wex, Brigitte (author)
التنسيق: article
منشور في: 2013
الوصول للمادة أونلاين:http://hdl.handle.net/10725/6498
https://doi.org/10.1016/j.jphotochem.2013.07.018
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.sciencedirect.com/science/article/pii/S1010603013003560
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author El-Ballouli, Alaa O.
author2 Khnayzer, Rony S.
Khalife, Jihane C.
Fonari, Alexandr
Hallal, Kassem M.
Timofeeva, Tatiana V.
Digambara, Patra
Wex, Brigitte
author2_role author
author
author
author
author
author
author
author_facet El-Ballouli, Alaa O.
Khnayzer, Rony S.
Khalife, Jihane C.
Fonari, Alexandr
Hallal, Kassem M.
Timofeeva, Tatiana V.
Digambara, Patra
Wex, Brigitte
author_role author
dc.creator.none.fl_str_mv El-Ballouli, Alaa O.
Khnayzer, Rony S.
Khalife, Jihane C.
Fonari, Alexandr
Hallal, Kassem M.
Timofeeva, Tatiana V.
Digambara, Patra
Wex, Brigitte
dc.date.none.fl_str_mv 2013
2017-11-03T10:45:39Z
2017-11-03T10:45:39Z
2017-11-03
dc.identifier.none.fl_str_mv 1873-2666
http://hdl.handle.net/10725/6498
https://doi.org/10.1016/j.jphotochem.2013.07.018
Ala’a, O., Khnayzer, R. S., Khalife, J. C., Fonari, A., Hallal, K. M., Timofeeva, T. V., ... & Kaafarani, B. R. (2013). Diarylpyrenes vs. diaryltetrahydropyrenes: Crystal structures, fluorescence, and upconversion photochemistry. Journal of Photochemistry and Photobiology A: Chemistry, 272, 49-57.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.sciencedirect.com/science/article/pii/S1010603013003560
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Journal of Photochemistry and Photobiology A: Chemistry
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Diarylpyrenes vs. diaryltetrahydropyrenes
crystal structures, fluorescence, and upconversion photochemistry
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description The synthesis of two series of substituted 2,7-diaryl-4,5,9,10-tetrahydropyrenes (1a–c) and 2,7-diarylpyrenes (2a–c) is reported; the opposing phenyl tips being terminated with tBu (a), OCH3 (b), or F (c) to impart variation in electronic properties. X-ray crystallographic analysis of the six compounds revealed edge-to-face packing predominately due to van der Waals forces in the solid state in all instances. The photophysical properties of these compounds were investigated in solution and in solid state/thin films. Since the 2,7-bis(4-tert-butylphenyl)tetrahydropyrene 1a possesses unity fluorescence quantum efficiency, it was successfully employed as the emitter in a low power upconversion scheme featuring fac-Ir(ppy)3 [ppy = 2-phenylpyridine] as the photosensitizer.
eu_rights_str_mv openAccess
format article
id LAURepo_c1fdff2c9cb101fa3449096359704b36
identifier_str_mv 1873-2666
Ala’a, O., Khnayzer, R. S., Khalife, J. C., Fonari, A., Hallal, K. M., Timofeeva, T. V., ... & Kaafarani, B. R. (2013). Diarylpyrenes vs. diaryltetrahydropyrenes: Crystal structures, fluorescence, and upconversion photochemistry. Journal of Photochemistry and Photobiology A: Chemistry, 272, 49-57.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/6498
publishDate 2013
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repository.name.fl_str_mv
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spelling Diarylpyrenes vs. diaryltetrahydropyrenescrystal structures, fluorescence, and upconversion photochemistryEl-Ballouli, Alaa O.Khnayzer, Rony S.Khalife, Jihane C.Fonari, AlexandrHallal, Kassem M.Timofeeva, Tatiana V.Digambara, PatraWex, BrigitteThe synthesis of two series of substituted 2,7-diaryl-4,5,9,10-tetrahydropyrenes (1a–c) and 2,7-diarylpyrenes (2a–c) is reported; the opposing phenyl tips being terminated with tBu (a), OCH3 (b), or F (c) to impart variation in electronic properties. X-ray crystallographic analysis of the six compounds revealed edge-to-face packing predominately due to van der Waals forces in the solid state in all instances. The photophysical properties of these compounds were investigated in solution and in solid state/thin films. Since the 2,7-bis(4-tert-butylphenyl)tetrahydropyrene 1a possesses unity fluorescence quantum efficiency, it was successfully employed as the emitter in a low power upconversion scheme featuring fac-Ir(ppy)3 [ppy = 2-phenylpyridine] as the photosensitizer.PublishedN/A2017-11-03T10:45:39Z2017-11-03T10:45:39Z20132017-11-03Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1873-2666http://hdl.handle.net/10725/6498https://doi.org/10.1016/j.jphotochem.2013.07.018Ala’a, O., Khnayzer, R. S., Khalife, J. C., Fonari, A., Hallal, K. M., Timofeeva, T. V., ... & Kaafarani, B. R. (2013). Diarylpyrenes vs. diaryltetrahydropyrenes: Crystal structures, fluorescence, and upconversion photochemistry. Journal of Photochemistry and Photobiology A: Chemistry, 272, 49-57.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttp://www.sciencedirect.com/science/article/pii/S1010603013003560enJournal of Photochemistry and Photobiology A: Chemistryinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/64982021-03-19T10:03:27Z
spellingShingle Diarylpyrenes vs. diaryltetrahydropyrenes
El-Ballouli, Alaa O.
status_str publishedVersion
title Diarylpyrenes vs. diaryltetrahydropyrenes
title_full Diarylpyrenes vs. diaryltetrahydropyrenes
title_fullStr Diarylpyrenes vs. diaryltetrahydropyrenes
title_full_unstemmed Diarylpyrenes vs. diaryltetrahydropyrenes
title_short Diarylpyrenes vs. diaryltetrahydropyrenes
title_sort Diarylpyrenes vs. diaryltetrahydropyrenes
url http://hdl.handle.net/10725/6498
https://doi.org/10.1016/j.jphotochem.2013.07.018
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.sciencedirect.com/science/article/pii/S1010603013003560