کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1336051 | 1500247 | 2015 | 11 صفحه PDF | دانلود رایگان |
Pd(II) chloride organometallics with 2-phenylpyridine and pyridines of general formula [Pd(2ppy∗)LCl] (2ppy∗ = C(2′)-deprotonated form of 2-phenylpyridine (2ppy), acting as N(1),C(2′)-chelating ligand; L = NH3, pyridine, 2-, 3-, 4-methylpyridine, 2,3-, 2,4-, 2,6-, 3,5-dimethylpyridine, 2,4,6-trimethylpyridine) were studied by 1H, 13C and 15N NMR. 1H, 13C and 15N NMR coordination shifts (i.e. differences of chemical shifts for the same atom in the complex and ligand molecules) were discussed in relation to the molecular structures. Single crystal X-ray structure of trans(N,N)-[Pd(2ppy∗)(2,4,6col)Cl] was solved. The analysis of 15N NMR coordination shifts for the whole series of the studied organometallics exhibited that all of them had an analogous trans(N,N) geometry.
1H, 13C and 15N NMR coordination shifts of [Pd(2-phenylpyridine∗)LCl] organometallics (2-phenylpyridine∗ = C(2′)-deprotonated form of 2-phenylpyridine (2ppy), acting as N(1),C(2′)-chelating ligand; L = NH3, pyridine, various mono-, di-, trimethylpyridines) exhibit that all compounds have the trans(N,N)-geometry like the X-ray studied [Pd(2-phenylpyridine∗)(2,4,6-trimethylpyridine)Cl] molecule.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 92, 28 May 2015, Pages 41–51