Dinuclear tethered pyridine, diimine complexes
نویسندگان
چکیده
منابع مشابه
Cyclopentadienyl chromium diimine and pyridine-imine complexes: ligand-based radicals and metal-based redox chemistry.
Paramagnetic CpCr(III) complexes with antiferromagnetically-coupled anionic radical diimine and pyridine-imine ligands were prepared and characterized. The diimine chloro CpCr[(ArNCR)(2)]Cl complexes (1: Ar = 2,6-iPr(2)C(6)H(3) (Dpp), R = H; 2: Ar = 2,6-Me(2)C(6)H(3) (Xyl), R = Me; 3: Ar = 2,4,6-Me(3)C(6)H(2) (Mes), R = Me) were synthesized by treatment of previously reported Cr(diimine)(THF)(2...
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The syntheses and X-ray crystal structures of dinuclear μ-azido and μ-nitrido bridged iridium complexes bearing the pyridine, diimine ligand (PDI) are reported. Their electronic structures and formal oxidation states of the metal centers are analyzed by theoretical and experimental methods, revealing the non-innocence of the PDI and nitrido ligands.
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Reduction of Cp*2UI(THF) with KC8 in the presence of a pyridine(diimine) ligand ((Mes)PDI(Me)) results in the formation of Cp*U(PDI)(THF), which features a triply reduced PDI ligand. This species performs four electron cleavage of azobenzene to generate the uranium bis(imido), Cp*(PDI)U(NPh)2.
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The electrochemical behaviour of the complexes [Re(CO)(3)X(α-diimine)], X = Cl or Br, α-diimine = 1,4-di-tert-butyl-1,4-diaza-1,3-diene, was reinvestigated using cyclic voltammetry accompanied by IR and UV-vis spectroelectrochemistry. While the reduction results in the loss of halide, as necessary for the electrocatalytic activity of related diimine compounds, a reversible oxidation could be ob...
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A series of dissymmetric dinuclear complexes were synthesized, as dual site catalysts in ethylene polymerization, by coupling the allylated a-diimine complexes of the metals Ti, Zr, V, Ni and Pd with the ansa-zirconocene complex [C5H4-SiH(Me)-C5H4]ZrCl2 possessing a hydride silane moiety. The different stages of syntheses included the formation of bis(cyclopentadienide)methyl silane which was u...
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ژورنال
عنوان ژورنال: Dalton Transactions
سال: 2018
ISSN: 1477-9226,1477-9234
DOI: 10.1039/c8dt02347f