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dc.contributor.author |
Yousfi, M |
|
dc.contributor.author |
Rahmani, Z |
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dc.contributor.author |
Saidi, M |
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dc.contributor.author |
Dakmouche, M |
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dc.date.accessioned |
2019-06-11T11:14:34Z |
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dc.date.available |
2019-06-11T11:14:34Z |
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dc.date.issued |
2013 |
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dc.identifier.uri |
http://e-biblio.univ-mosta.dz/handle/123456789/10813 |
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dc.description.abstract |
The aim of this work is to determine the partition coefficients log Pwo of eleven compounds, dithiolethiones, dithiolone, nitrone, 1.2-dithiole-3-imine and bromines compounds which is carried out by two experimental methods: UV-VIS and HPLC. According to the procedure of the traditional method shake-flask and we confirm the results by using a theoretical method for calculating the values of log Pwo. Another aim is to obtain the value of the unknown fragmental constant of imine (C= N) and the value found of imine fC= N underlined in the calculatation of log Pwo (N-p-nitrophenyl 5-phenyl-1.2-dithiole-3-imine); then to compare the calculated log Pwo value with the experimental. The results show that:(i) the dithiolones are more hydrophilic than the dithiolethiones;(ii) the values of log Pwo of derivatives bromines, imine and nitrone are lately given in experiments. Our analysis demonstrates good agreement between the experimentally observed and calculated log Pwo values. |
en_US |
dc.publisher |
Asian Journal of Chemistry |
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dc.subject |
Dithiolethiones |
en_US |
dc.subject |
Partition coef ficient |
en_US |
dc.subject |
Hydr ophobe |
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dc.title |
Experimental and theoretical study on lipophilicity of novel 1.2-dithiole-3-thiones synthetic |
en_US |
dc.type |
Article |
en_US |
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