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Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine
N,N-dimethyl-N′-picryl-4,4′-stilbenediamine (DMPSDA) was prepared, purified and crystallised in a form of black lustrous crystals, and its absorption and fluorescence spectra were recorded in cyclohexane, acetonitrile and dimethyl sulfoxide. Non-emissive intramolecular charge transfer state (ICT) wa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799324/ https://www.ncbi.nlm.nih.gov/pubmed/25106474 http://dx.doi.org/10.1007/s10895-014-1425-9 |
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author | Papper, Vladislav Wu, Yuanyuan Kharlanov, Vladimir Sukharaharja, Ayrine Steele, Terry W. J. Marks, Robert S. |
author_facet | Papper, Vladislav Wu, Yuanyuan Kharlanov, Vladimir Sukharaharja, Ayrine Steele, Terry W. J. Marks, Robert S. |
author_sort | Papper, Vladislav |
collection | PubMed |
description | N,N-dimethyl-N′-picryl-4,4′-stilbenediamine (DMPSDA) was prepared, purified and crystallised in a form of black lustrous crystals, and its absorption and fluorescence spectra were recorded in cyclohexane, acetonitrile and dimethyl sulfoxide. Non-emissive intramolecular charge transfer state (ICT) was clearly observed in this molecule in all three solvents. Theoretical calculations demonstrating a betaine electronic structure of the trinitrophenyl group in the ground state of the molecule and a charge transfer nature of the long wavelength transition S(0) → S(1) supported the experimental observations of the ICT formation in the molecule. |
format | Online Article Text |
id | pubmed-5799324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-57993242018-02-12 Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine Papper, Vladislav Wu, Yuanyuan Kharlanov, Vladimir Sukharaharja, Ayrine Steele, Terry W. J. Marks, Robert S. J Fluoresc Original Paper N,N-dimethyl-N′-picryl-4,4′-stilbenediamine (DMPSDA) was prepared, purified and crystallised in a form of black lustrous crystals, and its absorption and fluorescence spectra were recorded in cyclohexane, acetonitrile and dimethyl sulfoxide. Non-emissive intramolecular charge transfer state (ICT) was clearly observed in this molecule in all three solvents. Theoretical calculations demonstrating a betaine electronic structure of the trinitrophenyl group in the ground state of the molecule and a charge transfer nature of the long wavelength transition S(0) → S(1) supported the experimental observations of the ICT formation in the molecule. Springer US 2014-08-09 2018 /pmc/articles/PMC5799324/ /pubmed/25106474 http://dx.doi.org/10.1007/s10895-014-1425-9 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Papper, Vladislav Wu, Yuanyuan Kharlanov, Vladimir Sukharaharja, Ayrine Steele, Terry W. J. Marks, Robert S. Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title | Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title_full | Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title_fullStr | Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title_full_unstemmed | Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title_short | Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine |
title_sort | theoretical and experimental studies of n,n-dimethyl-n′-picryl-4,4′-stilbenediamine |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799324/ https://www.ncbi.nlm.nih.gov/pubmed/25106474 http://dx.doi.org/10.1007/s10895-014-1425-9 |
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