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(CO)5Cr(μ-CN)Cu(PPh3)3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

178693-52-2

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178693-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178693-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,6,9 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178693-52:
(8*1)+(7*7)+(6*8)+(5*6)+(4*9)+(3*3)+(2*5)+(1*2)=192
192 % 10 = 2
So 178693-52-2 is a valid CAS Registry Number.

178693-52-2Upstream product

178693-52-2Downstream Products

178693-52-2Relevant academic research and scientific papers

Cyanide-Bridged Heterobimetallic Complexes of the Group 6 Metal Carbonyls and Copper(I). X-ray Structures of (CO)5MCNCu(PPh3)3 (M = Cr, W) Derivatives

Darensbourg, Donald J.,Yoder, Jeffrey C.,Holtcamp, Matthew W.,Klausmeyer, Kevin K.,Reibenspies, Joseph H.

, p. 4764 - 4769 (1996)

The cyanide-bridged compounds (CO)5MCNCu(PPh3)3 where M = W in 1, and M = Cr in 2 have been prepared by the reaction of NaM(CO)5CN with Cu(CH3CN)4BF4 and PPh3, and their solid-state structures have been determined crystallographically. In 1, the CN bond length was 1.15(2) A?, and the bridge was slightly bent with angles of W-C(6)-N(1) = 175.9(14)° and Cu-N(1)-C(6) = 176(2)°. Crystal data for 1: monoclinic, space group P21/n, a = 20.376(4) A?, b = 12.436(3) A?, c = 22.423(5) A?, β= 97.28(3)°, Z = 4, R = 7.90percent. The chromium analog, complex 2, was isomorphous with 1. In addition, the isocyanide-bridged complex (CO)5WNCCu-(PPh3)3 (3) was prepared by the reaction of CuCN with PPh3 and W(CO)5(THF) at -78°C. The structure of this compound was determined by infrared and 13C NMR measurements. The isocyanide-bridged 3 was found to undergo thermal rearrangement to yield the cyanide-bridged 1. In the 13C NMR spectrum of 1 at room temperature, the CN peak is very broad (fwhh = 47 Hz) and can be found at 147.8 ppm. Dynamic 13C NMR measurements on 1 revealed that this complex undergoes an equilibrium reaction in THF-d8 solution. Two possibilities are presented which are consistent with the observations. One is a contact ion pair/solvent-separated ion pair exchange reaction which involves breakage of the Cu-N bond and insertion of a solvent molecule. The second is dissociation/ recoordination of a triphenylphosphine ligand from Cu(I). Differentiation between the two is impossible on the basis of the available data. In the slow-exchange limit, the 13CN peak of 1 is found at 149.0 ppm, shows 183W satellites (Jwc = 96 Hz), and has a line width of 12 Hz. In the 13C NMR spectrum of 3 at room temperature, the CN peak is sharp (fwhh = 0.75 Hz) and can be found at 160.7 ppm. Dynamic 13C NMR measurements on 3 revealed no ion pair exchange as high as 40°C. The 13C NMR spectrum of Cu13CN(PPh3)3 was also recorded at room temperature, and the CN peak can be found at 152.3 ppm with a line width of 15 Hz.

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