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Co2(μ-bis(tert-butylsulfonyl)ethyne)(CO)5(dibenzyl sulfide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

250129-22-7

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250129-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250129-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,1,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250129-22:
(8*2)+(7*5)+(6*0)+(5*1)+(4*2)+(3*9)+(2*2)+(1*2)=97
97 % 10 = 7
So 250129-22-7 is a valid CAS Registry Number.

250129-22-7Relevant academic research and scientific papers

Alkyne Dicobalt Carbonyl Complexes with Sulfide Ligands. Synthesis, Crystal Structure, and Dynamic Behavior

Verdaguer, Xavier,Moyano, Albert,Pericàs, Miquel A.,Riera, Antoni,Alvarez-Lárena, Angel,Piniella, Joan-F.

, p. 4275 - 4285 (2008/10/08)

Hexacarbonyl dicobalt complex of bis(tert-butylsulfonylethyne) [Co2(μ-ButSO2C)2(CO) 26, 3] experiences a thermally induced ligand exchange process with methyl p-tolyl sulfide, dibenzyl sulfide, and diethyl sulfide to give the corresponding stable sulfide complexes [Co2(μ-But-S02C)2(CO) 5SR2] 4, 5, and 6, respectively, in good yield (59-65%). The reaction with tetrahydrothiophene gives a disubstituted complex 7 in 74% yield. Oxathiane 9, derived from (+)-(2R)-10-mercaptoisoborneol, also reacts with 3 to generate a chiral sulfide complex 8 (58%). The solid-state structures of 5 and 8 have been established by X-ray crystallography and reveal the preference of the incoming sulfur ligand to occupy an equatorial coordination site. Further structural studies on 5 have been performed by low-temperature 1H NMR analysis and by theoretical procedures at the PM3(tm) level of theory. Analysis of the low-temperature 1H NMR spectrum of 5 shows a signal splitting consistent with the freezing of an equilibrium between two equatorially coordinated sulfides, and the computational study of the different isomers of 5 shows that the equatorially coordinated complex is 3.9 kcal mol-1 lower in energy than the most stable axially coordinated one, in agreement with solid-state and solution studies. Finally, ligand exchange experiments have been performed in order to provide an explanation for the Pauson - Khand reactivity of alkynes containing ancillary sulfide ligands and were found to support the experimentally observed rate enhancements.

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