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- W2034950254 abstract "Cyclopalladated azido dimers having various C,N-donor ligands, [Pd(μ-N3)(C,N-Ln)]2 (L1H = 2-(2′-thienyl)pyridine; L2H = azobenzene; L3H = 3,3′-dimethylazobenzene; L4H = N,N′-dimethylbenzylamine; L5H = 2-phenylpyridine), underwent cleavage with tertiary (or chelating) phosphines to form the cyclopalladated [Pd(N3)(PR3)(C,N-L)], the σ-bonded [Pd(N3)(PR3)2(C-L)], or the dinuclear-cyclopalladated [PdN3(PR3)(C,N-L)]2(μ-P∼P) complexes. In particular, treating [Pd(μ-N3)(C,N-L)]2 with the basic chelating phosphine (depe or dmpe) produced the homoleptic bis(chelating) complex [Pd(C,N-Ln)2] (n = 1–3). Complex [Pd(N3)(PR3)(C,N-L4)] or [Pd(N3)(PR3)2(C-L4)] reacted with aryl isocyanides to selectively give the imidoyl [Pd(N3)(–CN–Ar)(PR3)(N-L4)] or the imidoyl carbodiimido complex [Pd(NCN–Ar)(–CN–Ar)(PR3)(N-L4)], which was formed by the CN–Ar insertion into the orthometallated Pd–C bond on the phenyl moiety or the interaction into the Pd–N3 bond of the supporting ligand. In addition, reactions of [Pd(N3)(PR3)2(C-Ln)] (n = 1, 2, 4) with R–NCS {R = i-Pr, C6H4–NCS, (CH3)3Si} gave the S-coordinated tetrazole–thiolato Pd(II) complexes. Finally, the catalytic activity of the cyclopalladated azido complexes was evaluated." @default.
- W2034950254 created "2016-06-24" @default.
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- W2034950254 creator A5065385226 @default.
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- W2034950254 date "2009-01-01" @default.
- W2034950254 modified "2023-10-18" @default.
- W2034950254 title "Cyclopalladated azido complexes containing C,N-donor (HC∼N = 2-(2′-thienyl)pyridine, azobenzene, 3,3′-dimethyl azobenzene, N,N′-dimethylbenzylamine, 2-phenylpyridine) ligands: reactivity towards organic unsaturated compounds and catalytic properties" @default.
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- W2034950254 doi "https://doi.org/10.1039/b907324h" @default.
- W2034950254 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19672502" @default.
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