19680-83-2Relevant articles and documents
Molybdenum-catalyzed episulfidation of (E)-cycloalkenes with elemental sulfur
Adam,Bargon
, p. 1910 - 1911 (2001)
Episulfidation of (E)-cyclooctene and (E)-cyclononene was achieved with elemental sulfur by using a catalytic amount of a molybdenum oxo complex.
ORGANIC MOLYBDENUM COMPOUNDS AND LUBRICATING COMPOSITIONS COMPRISING SAID COMPOUNDS
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Page/Page column 60, (2008/12/07)
The present inventon provides organic molybdenum compounds which can be represented by the general formula (1) which is indicated below. General Formula (1) In this formula A1 and A2 are groups each selected individually from the group comprising heterocyclic rings, which may have substituent groups, and the dialkylamino groups.
Tris(dialkyldithiocarbamato)diazenido(1-) and hydrazido(2-) molybdenum complexes: Synthesis and reactivity in acid medium
Riveros, Pablo C.,Perilla, Isabel C.,Poveda, Arnulfo,Keller, Heimo J.,Pritzkow
, p. 2327 - 2335 (2008/10/08)
A series of new molybdenum complexes, [Mo(NNH-CO-Ph){S2CN (C2H5)2}3] (1), [Mo(NN-CO-C6H4-NO2){S2CN (C2H5)2}3] (2), [Mo(NNH-CO-Ph){S2CN(CH3)2}3] (3), [Mo(NN-CO-C6H4-NO2){S2CN (CH3)2}3] (4) have been synthesized, with p-nitrobenzoyldiazenido(1-) and benzoylhydrazido(2-) as ligands, and dialkyldithio-carbamatos as coligands. Reactions of these compounds with aqueous and methanolic HCl were carried out but the attempted separation of the aroyl group was unsuccessful. Only the reaction of 1 and 2 with HCl in methanol gave a product, identified as [Mo{S2CN(C2H5)2}4] [MoCl4(OCH3)2]. The complexes were characterized by elemental analysis, IR spectroscopy, 1H and 13C NMR, and mass spectrometry. Single crystals of 2 were obtained and the crystal structure was determined. The Mo atom is heptacoordinated; one diazenido(1-) and three diethyldithiocarbamatos act as ligands. From the latter one sulfur is in trans-position to the diazenido-nitrogen atom and the other five sulfur atoms lie in a plane giving a distorted pentagonal-bipyramidal coordination.
Aminomethylene complexes of divalent tungsten and molybdenum
Cook, Darren J.,Hill, Anthony F.
, p. 5616 - 5617 (2008/10/08)
Convenient routes are reported to aminomethylene complexes of divalent molybdenum and tungsten: [M(=CHNiPr2)(CO)2(S2CA)2] (M = Mo, W; A = NMe2, NEt2, N(CH2)4, OEt).
Reactions of chlorosilanes with dioxomolybdenum(VI) complexes
Arzoumanian, Henri,Krentzien, Heinz,Corao, Carolina,Lopez, Rafael,Agrifoglio, Giuseppe
, p. 2887 - 2892 (2008/10/09)
Various trialkylchlorosilanes were reacted with a number of molybdenum-oxo complexes in order to establish the main factors which influence the process of addition of the Si-Cl function across the Mo=O bond. A novel intermolecular mode of hexaalkyldisiloxane formation was observed in onecase.
Heterobinuclear Oxo-Bridged Complexes. III. CrIIIOMoV Compounds-Synthesis and Magnetic Properties
Elliot, Robyn L.,Kruger, Paul,Murray, Keith S.,West, Bruce O.
, p. 889 - 896 (2007/10/02)
Redox reactions between CrVO(P) (P is porphyrin dianion) and MoIVO(dtc)2 (dtc is a dithiocarbamate anion) result in the formation of two oxo-bridged CrIIIOMoIV compounds.The variation of magnetic susceptibility with temperature to 25 K shows evidence for strong antiferromagnetic coupling for the pyrrolidyldithiocarbamate complex with J = -300 cm-1.