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"W2(benzyl)2(O2CNMe2)4" is a complex organometallic compound consisting of a tungsten (W) core with two benzyl groups and four dimethylcarbamoyl ligands. The benzyl groups are organic molecules derived from benzene, with a methyl group attached to the benzene ring, while the dimethylcarbamoyl ligands are composed of a carbonyl group (C=O) bonded to a nitrogen atom, which in turn is bonded to two methyl groups. W2(benzyl)2(O2CNMe2)4 is characterized by its unique structure, where the tungsten atoms are bridged by the benzyl groups, and the dimethylcarbamoyl ligands coordinate to the tungsten, forming a complex with potential applications in catalysis and materials science. The specific arrangement and bonding of these groups give the compound its distinct chemical properties and reactivity.

84913-56-4

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84913-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84913-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,1 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84913-56:
(7*8)+(6*4)+(5*9)+(4*1)+(3*3)+(2*5)+(1*6)=154
154 % 10 = 4
So 84913-56-4 is a valid CAS Registry Number.

84913-56-4Upstream product

84913-56-4Downstream Products

84913-56-4Relevant academic research and scientific papers

The Tungsten-Tungsten Triple Bond. 14. Factors Influencing Triple Bonds between Tungsten Atoms Having Valence Molecular Orbital Configurations of ?2?4 and ?4δ2 and Preparation and Characterization of Bis(neopentyl)bis(acetato)bis(diethyldithiocarbamato)ditungsten

Chisholm, Malcolm H.,Clark, David L.,Huffman, John C.,Van Der Sluys, William G.

, p. 6817 - 6825 (1987)

Compounds having the general formula W2R2(O2CX)4 (R = an alkyl lacking β hydrogens; X = alkyl, aryl, NR2) adopt one of two basic structures with W-W triple bonds of approximate valence MO configurations of either ?4δ2 (I) or ?2?4 (II).The most common structure for X = alkyl or aryl is one in which the alkyl ligands, R, are aligned along the W-W axis and four O2CX ligands span a WW bond of ?4δ2 configuration (I).The other structure, found exclusively for X = NR2, is one in which there are mutually syn-alkyl ligands, and each W atom forms five W-L ? bonds that all lie roughly in a pentagonal plane with a resultant WW bond of ?2?4 configuration (II).Both steric and electronic factors are important in determining the choice of structure I or II.Bulky supporting ligands favor I and appear to show a discriminating factor R > X, but electronic factors can override these steric influences, as in the case of X = NR2.The reaction between W2(np)2(O2CMe)4 (np = neopentyl) and NaS2CNEt2 (2 equiv) in hexane in the presence of MeCOOH yields W2(np)2(O2CMe)2(S2CNEt2)2 with the transformation of the WW bond from ?4δ2 to ?2?4.The reaction between W2(np)2(O2CMe)4 and thioacetic O-acid (MeCOSH) yields W2(np)2(O2CMe)3(SOCMe) with retention of the axial W-np ligands and the ?4δ2 configuration of the WW bond.With the aid of Fenske-Hall calculations we show that there is essentially no electronic energy barrier to the interconversion of ?4δ2 and ?2?4 triple bonds.Conjugation between carboxylate and ? lone-pair orbitals of carbamate ligands has a destabilizing influence on the δ orbital in the ?4δ2 manifold, rendering it unstable with respect to the ?2?4 configuration.A similar effect is invoked in the conversion of W2(np)2(O2CMe)4 to W2(np)2(O2CMe)2(S2CNEt)2.Pertinent distances (Angstroem) for W2(np)2(O2CMe)2(S2CNEt2)2 are W-W = 2.2909 (10) Angstroem, W-O = 2.15 (1) Angstroem (averaged), W-S = 2.52 (1) Angstroem (averaged), and W-C = 2.19 (1) Angstroem.Crystal data (-160 deg C) are as follows: a = 17.092 (12) Angstroem, b = 11.023 (7) Angstroem, c = 17.576 (12) Angstroem, β = 98.19 (4)deg, dcalcd = 1.825 g cm-3, Z = 4, and space group P21/a.

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