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Bonding mode variations in palladium(II) and platinum(II) azaphosphole complexes: Identification by /sup 1/H, /sup 31/P, and /sup 195/Pt (NMR of N- and P-coordination, Pt-Cl addition to P, and dimerization

Journal Article · · Inorg. Chem.; (United States)
DOI:https://doi.org/10.1021/ic00288a012· OSTI ID:5708306
The 1,2,3-diazaphosphole P/double bond/C(H)C(Me)/double bond/NNMe (L/sub A/) and the 1,2,4,3-triazaphospholes P/double bond/NC(Ph)/double bond/NNMe (L/sub B/) and P/double bond/NN(Me)C(Me)/double bond/N (L/sub C/) react with the halo-bridged dimers (MX/sub 2/(PEt/sub 3/))/sub 2/ (M = Pt/sup II/, Pd/sup II/) to afford a variety of products with MX/sub 2/(PEt/sub 3/)L (L = di- or triazaphosphole) stoichiometry. With (PdCl/sub 2/(PEt/sub 3/))/sub 2/ these azaphospholes produce trans-(PdCl/sub 2/(PEt/sub 3/)L) with /sigma/-N-bonded L. From (PtBr/sub 2/(PEt/sub 3/))/sub 2/ is obtained (PtBr/sub 2/(PEt/sub 3/)L) as a mixture of the cis /sigma/-P coordination isomer with lesser amounts of the trans /sigma/-N isomer. These azaphospholes all afford different products with (PtCl/sub 2/(PEt/sub 3/))/sub 2/; the diazaphosphole L/sub A/ produces mononuclear cis-(PtCl/sub 2/(PEt/sub 3/)L/sub A/) (/sigma/-P bound) whereas the triazaphospholes L/sub B/ and L/sub C/ produce dinuclear species that have symmetric and asymmetric structures, respectively. The new air-sensitive complexes have been principally characterized by a combination of /sup 1/H, /sup 31/P, and /sup 195/Pt NMR solution spectroscopy. 23 refs., 8 figs., 3 tabs.
Research Organization:
Univ. of Amsterdam (Netherlands)
OSTI ID:
5708306
Journal Information:
Inorg. Chem.; (United States), Journal Name: Inorg. Chem.; (United States) Vol. 27:15; ISSN INOCA
Country of Publication:
United States
Language:
English

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