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"WCl2(CH2=CH2)2(PMePh2)2" is a complex organometallic compound, featuring a tungsten (W) center. It is characterized by two chloride (Cl) ligands, two ethylene (CH2=CH2) groups, and two diphenylphosphinoethane (PMePh2) ligands. The ethylene groups are coordinated to the tungsten atom, while the diphenylphosphinoethane ligands act as bidentate ligands, each donating two phosphorus atoms to the metal center. WCl2(CH2=CH2)2(PMePh2)2 is of interest in organometallic chemistry and catalysis due to its potential applications in various chemical transformations, such as olefin polymerization and cross-coupling reactions. The structure of the compound suggests that it could have a role in stabilizing reactive intermediates or facilitating specific types of bond formations, although its exact reactivity and applications would depend on further experimental investigation.

90245-67-3

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90245-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90245-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,4 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90245-67:
(7*9)+(6*0)+(5*2)+(4*4)+(3*5)+(2*6)+(1*7)=123
123 % 10 = 3
So 90245-67-3 is a valid CAS Registry Number.

90245-67-3Relevant academic research and scientific papers

Reactions of WCl2L4 (L = a phosphine). 1. A new class of tungsten(II) ethylene complexes

Sharp, Paul R.

, p. 1217 - 1223 (1984)

WCl2L4 can be prepared by reducing WCl4Ln with 2 equiv of sodium amalgam in the presence of L (L = PMe3, n = 3; L = PMe2Ph and PMePh2, n = 2). Phosphine is displaced from WCl2L4 by ethylene to give first WCl2L3(C2H4) (L = PMe3) and then WCl2L2(C2H4)2. WCl2(PMe3)2(C2H4) 2 reacts with TlBF4, AlCl3, and AlMe3 to give cationic complexes. The X-ray crystal structure of one of these, [WMe-(PMe3)2(C2H4) 2][ClAlMexCl3-x], was determined. The crystals are monoclinic (P21/n) with a = 9.922 (2) ?, b = 7.419 (1) ?, c = 29.241 (4) ?, β = 92.79 (2)°, V = 2150 ?3, and Z = 4. The three-dimensional X-ray data were measured with the θ-2θ scan technique with a scintillation detector. The structure was resolved by Patterson and Fourier methods and refined by full-matrix least-squares calculations to give R(Fo) = 0.025 and Rw(Fo) = 0.032 for 1362 observations above 2σ. The solid state structure consists of monomeric units with cis ethylenes, trans phosphines, and a weakly coordinated aluminate. NMR and conductivity data suggest the equilibrium in solution of this structure with an ionic complex formed by loss of the aluminate. The reaction of this complex with tmeda (N,N,N′,N′ -tetramethylethylenediamine) or other Lewis bases gives neutral WMeCl(PMe3)2(C2H4)2 that loses Cl- in polar, noncoordinating solvents.

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