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Author(s):
Al-Ajlouni, A. M.; Gunyar, A.; Zhou, M. D.; Baxter, P. N. W.; Kuhn, F. E.
Title:
Adduct Formation of Dichloridodioxidomolybdenum(VI) and Methyltrioxidorhenium(VII) with a Series of Bidentate Nitrogen Donor Ligands
Abstract:
The stability of a variety of bidentate N-base adducts of MoO(2)Cl(2) and (CH(3))ReO(3) (MTO) was investigated in thf and CH(2)Cl(2) as solvents. The formation constants were determined from the spectrophotometric data based on 1:1 adduct formation. The adduct formation constants for [MoO2Cl(2)L(2)] (L(2) = bidentate nitrogen ligand) are 10(4)-10(6) times higher than those for [(CH(3))ReO(3)L(2)] with the same ligands under the same conditions. The adduct stability of both systems is very sensitive to the electronic nature of the ligands and increases with their donor ability. Hammett correlations of the formation constants against sigma give relatively large negative values for the reaction constants (rho(Re) = -5.9, rho(Mo) = -6.6). The stability is also governed by steric and strain factors. Thus, sterically hindered 6,6'-disubstituted-2,2'-bipyridines do not form adducts with MTO, and only 6,6'-dimethyl- and 6,6'-diphenyl-2,2'-bipyridines form adducts with MoO(2)Cl(2). However, these adducts are much less stable than other methyl derivatives of 2,2'-bipridine adducts. The steric strain between the two methyl groups in 3,3-dimethyl-2,2'-bipyridine influences the bipyridine planarity upon complexation and reduces the adduct stability. The thermodynamic parameters (enthalpy and entropy) were determined from temperature-dependence studies. The adduct stability is mainly due to the strongly exothermic binding of the nitrogen-bidentate ligand. The entropy change is small and has little effect on adduct stability. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Congress title:
ISI Document Delivery No.: 426BT Times Cited: 13 Cited Reference Count: 61 Al-Ajlouni, Ahmad M. Guenyar, Alev Zhou, Ming-Dong Baxter, Paul N. W. Kuehn, Fritz E. Kuhn, Fritz/A-3113-2010 Alexander von Humboldt Foundation; Bavarian elite network NanoCat A. M. A. thanks the Alexander von Humboldt Foundation for a Georg Forster Fellowship. A. G. acknowledges the Bavarian elite network NanoCat for it Ph. D. grant and for financial Support of the project. M.-D. Z. thanks the International Graduate Sch...     »
Journal title:
European Journal of Inorganic Chemistry
Year:
2009
Journal issue:
8
Pages contribution:
1019-1026
Fulltext / DOI:
doi:10.1002/ejic.200801103
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