Experimental and quantum-chemical studies of N-15 NMR coordination shifts in palladium and platinum chloride complexes with pyridine, 2,2 '-bipyridine and 1,10-phenanthroline

Warning

This publication doesn't include Faculty of Economics and Administration. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

PAZDERSKI Leszek SZLYK Edward SITKOWSKI Jerzy KAMIENSKI Bohdan KOZERSKI Lech TOUŠEK Jaromír MAREK Radek

Year of publication 2006
Type Article in Periodical
Magazine / Source Magnetic Resonance in Chemistry
MU Faculty or unit

Faculty of Science

Citation
Web DOI: 10.1002/mrc.1740
Doi http://dx.doi.org/10.1002/mrc.1740
Field Physical chemistry and theoretical chemistry
Keywords NMR; Quantum chemical calculations
Description A series of Pd and Pt chloride complexes with pyridine (py), 2,2'-bipyridine (bpy) and 1,10-phenanthroline (phen), of general formulae trans-/cis-[M(pY)(2)Cl-2], [M(py)(4)]Cl-2, trans-/cis-[M(py)(2)Cl-4], [M(bpy)Cl-2], [M(bPy)Cl-4], [M(phen)Cl-2], [M(phen)Cl-4], where M = Pd, Pt, was studied by H-1, Pt-195, and N-15 NMR. The 90-140 ppm low-frequency N-15 coordination shifts are discussed in terms of such structural features of the complexes as the type of platinide metal, oxidation state, coordination sphere geometry and the type of ligand. The results of quantum-chemical NMR calculations were compared with the experimental N-15 coordination shifts, well reproducing their magnitude and correlation with the molecular structure.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.