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				<datestamp>2011-12-31T08:09:40Z</datestamp>
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	<dc:title xml:lang="en-US">Studies on ion-pairing effects of the kinetics of aquation of bromopentaammine cobalt(III) complex in malonate media</dc:title>
	<dc:creator>Zeitouni, Farah Samih</dc:creator>
	<dc:creator>El-Subruiti, Gehan Moustafa</dc:creator>
	<dc:creator>Younes, Ghassan Omar</dc:creator>
	<dc:creator>Amira, Mohammad Fawzi</dc:creator>
	<dc:subject xml:lang="en-US">Ion-pair</dc:subject>
	<dc:subject xml:lang="en-US">Aquation</dc:subject>
	<dc:subject xml:lang="en-US">Solvent effect</dc:subject>
	<dc:subject xml:lang="en-US">Cobalt(III) complex</dc:subject>
	<dc:subject xml:lang="en-US">Dicarboxylic acid</dc:subject>
	<dc:subject xml:lang="en-US">Tert-butanol</dc:subject>
	<dc:description xml:lang="en-US">The aquation of bromopentaamminecobalt(III) ion in the presence of ion-pairing malonate anion in mixed solvent media of water with tert-butanol (10%-50%) v/v have been investigated spectrophotometrically at different temperatures (30-60 oC). Nonlinear plots of Log (kip) ion-pair rate constants against the reciprocal of the dielectric constant D, Log of water concentration and Grunwald-Winstein Y values were found. The thermodynamic and extrathermodynamic analyses of the kinetic data have been discussed in terms of solvent effect on the ion-pair aquation reactions. The obtained isokinetic temperatures of these systems indicate the existence of compensation effect arising from solute-solvent interaction. The extrema found in the change of ∆Hip* and ∆Sip*with the mole fraction of the co-solvent can be attributed to the change of the physical properties of the solvent-water mixture with the solvent structure. Application of a free energy cycle is performed to compare between the stability of the initial and the transition state of the complex. However, small changes in ∆Gip*with the mole fraction of the co-solvent was found, indicating a compensating effects between ∆Hip* and ∆Sip*</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-12-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/440</dc:identifier>
	<dc:identifier>10.5155/eurjchem.2.4.489-494.440</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 4 (2011): December 2011; 489-494</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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