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  • Articles: DFG German National Licenses  (2)
  • Physical Chemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 705-711 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dioxotetracyanomolybdate(IV) has been found to form a 1 : 2 complex with 2,2′-bipyridyl. The kinetics of the reaction has been studied over the pH range 5.3-8.7 by visible spectrophotometry under pseudo conditions. The effect of the 2,2′-bipyridyl and dioxotetracyanomolybdate(IV), temperature, ionic strength, and pH on the reaction rate was determined. The reaction follows first-order kinetics with respect to dioxotetracyanomolybdate(IV) ion and fractional-order kinetics with respect to 2,2′-bipyridyl. Values for the outer-sphere complex formation constant (Kos2) and rate constants (k2) were also calculated from the kinetic data. It was found that rate of the reaction increases with the decreasing pH. The following rate equation based on the outersphere complexation equilibrium preceding the associative interchange has been derived.\documentclass{article}\pagestyle{empty}\begin{document}$$\rm {{1}\over{{\it k}_{obs}}}={{1+K_{a2}[H^+]}\over{B_1[2,2\prime-bipyridyl]}}+B_2$$ ${\rm where}$ $\rm B_1={\it k}_1K_{os1}+{\it k}_2K_{os2}[H^+]K_{a2}$ ${\rm and}$ $\rm B_2={{K_{os1}+K_{a2}K_{os2}[H^+]}\over {{\it k}_1K_{os1}+{\it k}_2K_{os2}[H^+]K_{a2}}}.$\end{document}On the basis of the observed results probable mechanism has been proposed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 819-824 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An investigation is presented on the kinetics of complexation of aqueous solution of octacyanomolybdate (IV) and -tungstate (IV) after photoinitiation with one of the mixed group ligands containing both N and O, diethanolamine (DEOA), [NH(CH2CH2OH)2]. Under the steady state conditions and with approximation k3 〉 k4 over a range of concentrations, the observed rate law is:\documentclass{article}\pagestyle{empty}\begin{document}$$ \cal{k}_{\rm obs.}={\cal{k}_{2}\cal{k}_{4}\rm {I}_{a}[\rm {OH}^{-}][\rm {NH}(\rm{CH}_{2}\rm{CH}_{2}\rm{OH})_{2}]\over \rm{I}+\it \cal{k}_{2}[\rm {OH}^{-}]} $$\end{document}The complexes show shift in electronic transition supporting the mechanism of association of the ligand followed by the abstraction of some small molecules and then substitution by the ligand. The presence of the specific isobestic point also contributes towards the stability of the complex. The rate constant and quantum yield values are dependent on both the concentration of the metal cyanide and the ligand predicting the mechanism to be an associative one. The complexes have strong absorption in the visible range and are assigned metal-to-ligand electron transfer transition. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 819-824, 1997
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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