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Synthesis, spectroscopy, and X-ray structures of fac-(CO)3(dppe)MnSC(S)H, fac-(CO)3(dppe)ReSC(S)H, fac-(CO)3(dppp)ReSC(S)H, and fac-(CO)3(dppb)ReSC(S)H
Authors:Jaquay Cook  Ashleigh Hicks  Tyan Frazier  David M Kimari  Theodore A Budzichowski  Jeanette A Krause Bauer  Santosh K Mandal
Institution:(1) Department of Chemistry, Morgan State University, Baltimore, Maryland, 21251;(2) Department of Chemistry, University of Maryland Baltimore County, Baltimore, Maryland;(3) Department of Chemistry, University of Cincinnati, Cincinnati, Ohio
Abstract:The monodentate dithioformato complexes, fac-(CO)3(dppe)MnSC(S)H (1), fac- (CO)3(dppe)ReSC(S)H (2), fac-(CO)3(dppp)ReSC(S)H (3), and fac-(CO)3 (dppb)ReSC(S)H (4), where dppe is 1,2-bis(diphenylphosphino)ethane, dppp is 1,3-bis(diphenylphosphino)propane, and dppb is 1,4-bis(diphenylphosphino)butane, were synthesized from the treatment of the corresponding hydrides, fac-(CO)3 (P-P)MSC(S)H with CS2. Compounds 1–4 crystallize in the monoclinic crystal system: for 1, space group = P21/c, a = 15.3139(3) Å, b = 9.7297(4) Å, c = 19.0991(6) Å, beta = 105.928(1)cir, V = 2736.5 Å3, Z = 4; for 2, space group = P21/c, a = 15.6395(8) Å, b = 9.8182(5) Å, c = 19.4153(11) Å, beta = 106.741(1)cir, V = 2854.9(3) Å3, Z = 4; for 3, space group = P21/n, a = 11.3570(10) Å, b = 19.465(2) Å, c = 15.5702(14) Å, beta = 104.776(2)cir, V = 3328.3(5) Å3, Z = 4; and for 4, space group = C2/c, a = 32.078(2) Å, b = 10.4741(6) Å, c = 19.0608(9) Å, beta = 94.315(2)cir, V = 6386.1(6) Å3, Z = 8.
Keywords:Dithioformato complexes  X-ray crystal structure  monodentate bonding mode  synthesis
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