Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base

In this article, we have introduced an intermediate benzyl carbocation (formed as a result of photoionization) which serves as precursor for the synthesis of Schiff’s base. Lifetimes of many carbocations were determined from our laboratory. During the determination of the lifetimes, our endeavor was...

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Main Authors: R. Sanjeev, V. Jagannadham, R. V. Vrath, R. Ravi
Format: Article
Language:English
Published: Chemical Society of Ethiopia 2014-05-01
Series:Bulletin of the Chemical Society of Ethiopia
Subjects:
Online Access:http://www.ajol.info/index.php/bcse/article/view/103691
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author R. Sanjeev
V. Jagannadham
R. V. Vrath
R. Ravi
author_facet R. Sanjeev
V. Jagannadham
R. V. Vrath
R. Ravi
author_sort R. Sanjeev
collection DOAJ
description In this article, we have introduced an intermediate benzyl carbocation (formed as a result of photoionization) which serves as precursor for the synthesis of Schiff’s base. Lifetimes of many carbocations were determined from our laboratory. During the determination of the lifetimes, our endeavor was to obtain a carbocation with high selectivity, s = knu/kH2O. The selectivity is the ratio of the rate constant of the reaction of carbocation with an externally added nucleophile, (nu, aniline) to that of the rate constant of the water. Our intention was to obtain a carbocation with high selectivity, so that one can pave a path for the synthesis of Schiff’s base by the reaction of the carbocation intermediate with aniline. DOI: http://dx.doi.org/10.4314/bcse.v28i2.13
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spelling doaj.art-6ecd63a5699a4d57933b36b5b8522c912022-12-22T02:37:51ZengChemical Society of EthiopiaBulletin of the Chemical Society of Ethiopia1011-39241726-801X2014-05-0128129530010.4314/bcse.v28i2.13Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s baseR. SanjeevV. JagannadhamR. V. VrathR. RaviIn this article, we have introduced an intermediate benzyl carbocation (formed as a result of photoionization) which serves as precursor for the synthesis of Schiff’s base. Lifetimes of many carbocations were determined from our laboratory. During the determination of the lifetimes, our endeavor was to obtain a carbocation with high selectivity, s = knu/kH2O. The selectivity is the ratio of the rate constant of the reaction of carbocation with an externally added nucleophile, (nu, aniline) to that of the rate constant of the water. Our intention was to obtain a carbocation with high selectivity, so that one can pave a path for the synthesis of Schiff’s base by the reaction of the carbocation intermediate with aniline. DOI: http://dx.doi.org/10.4314/bcse.v28i2.13http://www.ajol.info/index.php/bcse/article/view/103691CarbocationSelectivityIntermediatesSolvolysisPhotoionization and Iminodiazonium ion
spellingShingle R. Sanjeev
V. Jagannadham
R. V. Vrath
R. Ravi
Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
Bulletin of the Chemical Society of Ethiopia
Carbocation
Selectivity
Intermediates
Solvolysis
Photoionization and Iminodiazonium ion
title Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
title_full Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
title_fullStr Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
title_full_unstemmed Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
title_short Intermediate obtained from photoionization, serving as precursor for the synthesis of Schiff’s base
title_sort intermediate obtained from photoionization serving as precursor for the synthesis of schiff s base
topic Carbocation
Selectivity
Intermediates
Solvolysis
Photoionization and Iminodiazonium ion
url http://www.ajol.info/index.php/bcse/article/view/103691
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