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- W2079270930 abstract "The diorganophosphinous-N-(N′, N′, N″, N″-tetramethyl) guanidinides 1a and 1b and the organophosphonous-bis-N-(N′, N′, N″, N″-tetramethyl)guanidinides 2 and 3 are used as ligands towards carbonyls of zerovalent transition metals. In most cases coordination via phosphorus is observed. 1b and 2 act as PN-donors towards the (tetracarbonyl)molybdenum fragment, forming chelate complexes involving one five-membered ring. 3 acts as a PNN′-donor towards molybdenum carbonyls, forming a bicyclic chelate complex. X-ray structure determinations were performed for the octacarbonyldimanganese compound 7, the tricarbonylnickel complex 8 and the tetracarbonyliron derivative 10. The dimanganese compound 7 was found to be diaxially substituted with short MnC bonds but standard MnP bond lengths. The nickel compound 8 exhibited short PNi bonds, long NiC bonds and short CO bonds, consistent with enhanced π-back donation from metal to phosphorus. The coordination geometry at the iron atom in 10 was found to be trigonal bipyramidal with phosphorus in the axial position, strongly distorted towards square pyramidal." @default.
- W2079270930 created "2016-06-24" @default.
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- W2079270930 date "1997-02-01" @default.
- W2079270930 modified "2023-09-24" @default.
- W2079270930 title "N-(N′, N′, N″, N″-tetramethyl) guanidine-substituted phosphines as monodentate, bidentate or tridentate ligands in transition metal chemistry" @default.
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- W2079270930 doi "https://doi.org/10.1016/s0022-328x(96)06444-3" @default.
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