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Investigation of the Reactivity of Phosphate Esters.

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dc.contributor.author Dr. M. Younas
dc.date.accessioned 2021-07-06T09:54:37Z
dc.date.available 2021-07-06T09:54:37Z
dc.date.issued 1984-06-01
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/12315
dc.description.abstract It is a well recognised fact that phosphate esters play a vital role in Living system. There is hardly any thing going on in the living cell that does not involve phosphate esters in one form or the other. To understand the chemistry of life it is necessary to understand the behaviour of simple phosphate esters, acting as model compounds for naturally occurring substances, particularly towards hydrolysis. Although phosphate mono- and diesters have been thoroughly investigated, only scattered information is available about the phosphate triesters. In the present investigation, three phosphate triesters belonging to the series diphenyl substituted-aryl phosphates have been prepared and the rates of their hydrolysis to diphenyl phosphate with the release of a phenolate anion, under different conditions, have been measured. As a result of these investigations, a general pattern of their behaviour towards hydrolysis has become clear and an extended study leading to the possible mechanistic interpretations of the biological reactions, can now conveniently be made. It has also been observed that the alkaline hydrolysis of diphenyl p-nitrophenyl phosphate is catalysed by β-Cyclodextrin, suggesting that cyclodextrin might be a suitable species for catalysing the hydrolysis reactions of a wide variety of organic phosphate esters en_US
dc.description.sponsorship PSF en_US
dc.language.iso en en_US
dc.publisher Institute of Chemistry, University of the Punjab, Lahore-1. en_US
dc.relation.ispartofseries (PP-05);PSF/RES/P-PU/CHEM(130)
dc.title Investigation of the Reactivity of Phosphate Esters. en_US
dc.type Technical Report en_US


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