Lewis-base-catalyzed diimine-ligand-substitution reactions at copper(I)

التفاصيل البيبلوغرافية
العنوان: Lewis-base-catalyzed diimine-ligand-substitution reactions at copper(I)
المؤلفون: Gerhard Geier, Urs M. Frei
المصدر: Inorganic Chemistry. 31:3132-3137
بيانات النشر: American Chemical Society (ACS), 1992.
سنة النشر: 1992
مصطلحات موضوعية: Substitution reaction, chemistry.chemical_classification, Reaction mechanism, Chemistry, Stereochemistry, Ligand, Iodide, Medicinal chemistry, Inorganic Chemistry, chemistry.chemical_compound, Nucleophile, Lewis acids and bases, Physical and Theoretical Chemistry, Acetonitrile, Diimine
الوصف: Substitutions of 2,2'-biguinoline (biq) in Cu(biq) 2 + by 2,9-dimethylphenanthroline (dmp) and 1,10-phenanthroline (phen), in acetone, were found to be catalyzed by Lewis bases, L. The catalyzed pathway involves an intermediate mixed-ligand complex Cu(biq)L + , in which L is rapidly replaced by the incoming diimine ligand. The individual rate constants for L=iodide and acetonitrile were evaluated. Analysis of the respective rate constants, together with the equilibrium constants, clearly shows that the better nucleophile, iodide, is the more efficient catalyst
تدمد: 1520-510X
0020-1669
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c6da21e077cc03d57fcd7962bdddcfc7Test
https://doi.org/10.1021/ic00040a025Test
رقم الانضمام: edsair.doi...........c6da21e077cc03d57fcd7962bdddcfc7
قاعدة البيانات: OpenAIRE