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[Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2]

Base Information Edit
  • Chemical Name:[Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2]
  • CAS No.:960069-54-9
  • Molecular Formula:C26H35Mo2O3P
  • Molecular Weight:618.416
  • Hs Code.:
  • Mol file:960069-54-9.mol
[Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2]

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Chemical Property of [Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2] Edit
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Technology Process of [Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2]

There total 1 articles about [Mo2(η5-cyclopentadienyl)2(μ-dicyclohexylphosphide)(μ-methoxycarbyne)(carbonyl)2] 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 toluene; byproducts: CO; (N2); stirring toluene soln. of molybdenum compd. at 333 K for 45 min; evapn., addn. of CH2Cl2 and petroleum ether, chromy. (alumina, CH2Cl2/petroleum ether (1:2)) at 253 K, evapn., elem. anal.;
DOI:10.1021/om700735g
Guidance literature:
In toluene; under N2, Schlenk techniques; HCCCOOMe added to soln. of Mo2Cp2(μ-COMe)(μ-PCy2)(CO)2 in toluene, mixt. stirred at 333 K for 2 h; evapn. under vac., residue extd. with CH2Cl2/petroleum ether (1/5), extract chromd. (Al2O3, 273 K); elem. anal.;
DOI:10.1016/j.jorganchem.2010.03.020
Guidance literature:
In toluene; under N2, Schlenk techniques; MeOOCCCCOOMe added to soln. of Mo2Cp2(μ-COMe)(μ-PCy2)(CO)2 in toluene, mixt. stirred at 333 K for 2.5 h; evapn. under vac., residue extd. with THF/petroleum ether (1/4), extractchromd. (Al2O3, 253 K), cis-isomer (44%) eluted with THF/petroleum ethe r (1/4), trans-isomer (39%) eluted with THF/petroleum ether (1/1);
DOI:10.1016/j.jorganchem.2010.03.020
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