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mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten

Base Information
  • Chemical Name:mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten
  • CAS No.:118050-80-9
  • Molecular Formula:C32H30O3P2S2W
  • Molecular Weight:772.518
  • Hs Code.:
mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten

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Chemical Property of mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten
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Technology Process of mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten

There total 2 articles about mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithioacetate)tungsten which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In ethanol; acetone; byproducts: CO; Irradiation (UV/VIS); a soln. of W(CO)4(dpp) in acetone is irradiated (125 W-Hg-high pressure lamp), solvent is removed in vac., residue is dissolved at -20°C in a soln. of methyldithioacetate in ethanol, suspn. is warmed to room temp. (under inert gas atmosphere).; ppt. is filtered off, washed with ethanol and dried in vac.; elem. anal.;
DOI:10.1016/0022-328X(87)80246-2
Guidance literature:
In tetrahydrofuran; euilibrium reaction;; mixt. of 65% fac-isomer and 35% mer-isomer obtained; detected by IR and (31)P-NMR-spectroscopy;
DOI:10.1016/0022-328X(87)80246-2
Guidance literature:
With CH3I; In tetrahydrofuran; addn. of CH3I to a soln. of isomer mixt. of the W-compd.; mixt. is kept at room temp. for 3 days; filtration; evapn. of filtrate to dryness; dissolving of residue in ethanol; addn. of NH4PF6 in ethanol/H2O; (under inert gas atmosphere); crystn. at 0°C; isomeric mixt. obtained; elem. anal.;
DOI:10.1016/0022-328X(87)80247-4
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