Excited-state relaxation of some aminoquinolines

<p>The absorption and fluorescence spectra, fluorescence quantum yields and lifetimes, and fluorescence rate constants (<mml:math> <mml:mrow> <mml:msub> <mml:mi>k</mml:mi> <mml:mi>f</mml:mi> </mml:msub> </mml:mrow> </mm...

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Format: Article
Language:English
Published: Hindawi Limited 2006-01-01
Series:International Journal of Photoenergy
Online Access:http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IJP/2006/35610
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spelling doaj-54d24ee6ec24462695014c259175337b2020-11-24T23:02:05ZengHindawi LimitedInternational Journal of Photoenergy1110-662X2006-01-012006Excited-state relaxation of some aminoquinolines<p>The absorption and fluorescence spectra, fluorescence quantum yields and lifetimes, and fluorescence rate constants (<mml:math> <mml:mrow> <mml:msub> <mml:mi>k</mml:mi> <mml:mi>f</mml:mi> </mml:msub> </mml:mrow> </mml:math>) of 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzoxazolyl)quinoline (<bold>I</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzothiazolyl)quinoline (<bold>II</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-methoxybenzothiazolyl)-quinoline (<bold>III</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzothiazolyl)benzoquinoline (<bold>IV</bold>) at different temperatures have been measured. The shortwavelength shift of fluorescence spectra of compounds studied (23&#8211;49 nm in ethanol) as the temperature decreases (the solvent viscosity increases) points out that the excited-state relaxation process takes place. The rate of this process depends essentially on the solvent viscosity, but not the solvent polarity. The essential increasing of fluorescence rate constant <mml:math> <mml:mrow> <mml:msub> <mml:mi>k</mml:mi> <mml:mi>f</mml:mi> </mml:msub> </mml:mrow> </mml:math> (up to about 7 times) as the solvent viscosity increases proves the existence of excited-state structural relaxation consisting in the mutual internal rotation of molecular fragments of aminoquinolines studied, followed by the solvent orientational relaxation.</p>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IJP/2006/35610
collection DOAJ
language English
format Article
sources DOAJ
title Excited-state relaxation of some aminoquinolines
spellingShingle Excited-state relaxation of some aminoquinolines
International Journal of Photoenergy
title_short Excited-state relaxation of some aminoquinolines
title_full Excited-state relaxation of some aminoquinolines
title_fullStr Excited-state relaxation of some aminoquinolines
title_full_unstemmed Excited-state relaxation of some aminoquinolines
title_sort excited-state relaxation of some aminoquinolines
publisher Hindawi Limited
series International Journal of Photoenergy
issn 1110-662X
publishDate 2006-01-01
description <p>The absorption and fluorescence spectra, fluorescence quantum yields and lifetimes, and fluorescence rate constants (<mml:math> <mml:mrow> <mml:msub> <mml:mi>k</mml:mi> <mml:mi>f</mml:mi> </mml:msub> </mml:mrow> </mml:math>) of 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzoxazolyl)quinoline (<bold>I</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzothiazolyl)quinoline (<bold>II</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-methoxybenzothiazolyl)-quinoline (<bold>III</bold>), 2-amino-3-(<mml:math> <mml:msup> <mml:mn>2</mml:mn> <mml:mo>&#x2032;</mml:mo> </mml:msup> </mml:math>-benzothiazolyl)benzoquinoline (<bold>IV</bold>) at different temperatures have been measured. The shortwavelength shift of fluorescence spectra of compounds studied (23&#8211;49 nm in ethanol) as the temperature decreases (the solvent viscosity increases) points out that the excited-state relaxation process takes place. The rate of this process depends essentially on the solvent viscosity, but not the solvent polarity. The essential increasing of fluorescence rate constant <mml:math> <mml:mrow> <mml:msub> <mml:mi>k</mml:mi> <mml:mi>f</mml:mi> </mml:msub> </mml:mrow> </mml:math> (up to about 7 times) as the solvent viscosity increases proves the existence of excited-state structural relaxation consisting in the mutual internal rotation of molecular fragments of aminoquinolines studied, followed by the solvent orientational relaxation.</p>
url http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IJP/2006/35610
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