Electrooxidation of molybdenum halide complexes of the type CpMo(CO)3−n(PR3)nX
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference12 articles.
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4. Electrochemical oxidation-reduction of carbonyl(η-cyclopentadienyl) dichalcogenocarbamatomolybdenum(II), (η-C5H5)Mo(CO)n (XYCNMe2) (n = 2, XY SeSe, SeS, SS, SeO, SO; n = 3, XY SeO, SO)
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1. Electrochemical study of methylfulvalene and methylcyclopentadiene molybdenum complexes;Journal of Organometallic Chemistry;1998-10
2. Stabilization of 17-electron metal-centered species. Electrochemical study of [WX(CO)3(η5-C5H5)] (X=Cl, Br, I) and [WI(CO)2(PCy3)(η5-C5H5)];Journal of Organometallic Chemistry;1998-03
3. Four-legged piano stool molybdenum(II) compounds without carbonyl ligands—3 cyclopentadienyl and indenyl complexes containing the tridentate ligand Ph2PCH2CH2P(Ph)CH2CH2PPh2(triphos) via reduction of molybdenum(III) precursors;Polyhedron;1996-07
4. The Organometallic Chemistry of Halocarbonyl Complexes of Molybdenum(II) and Tungsten(II);Advances in Organometallic Chemistry;1996
5. Cyclopentadienyl Complexes of Chromium, Molybdenum and Tungsten;Comprehensive Organometallic Chemistry II;1995
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