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Ir(OCH(CH3)2)(C12H6F4)(P(C6H11)3) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167425-07-2

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167425-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167425-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,2 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167425-07:
(8*1)+(7*6)+(6*7)+(5*4)+(4*2)+(3*5)+(2*0)+(1*7)=142
142 % 10 = 2
So 167425-07-2 is a valid CAS Registry Number.

167425-07-2Relevant academic research and scientific papers

Oxidative addition of HSnR3 (R = Ph, nBu) to the square-planar iridium(I) compounds Ir(XR)(TFB)(PCy3) (XR = OMe, OEt, OiPr, OPh, SnPr) and Ir(C2Ph)L2(PCy3) (L2 = TFB, 2CO)

Esteruelas, Miguel A.,Lahoz, Fernando J.,Oliván, Montserrat,O?ate, Enrique,Oro, Luis A.

, p. 3486 - 3496 (2008/10/09)

The synthesis of the compounds Ir(OR)(TFB)(PCy3) (R = Et (2), iPr (3), Ph (4); TFB = tetrafluorobenzobarrelene), Ir2(CO)6(PCy3)2 (5), Ir(SnPr)(TFB)(PCy3) (6), [Ir(μ-SnPr)(CO)-(PCy3)]2 (7), Ir(C2R)(TFB)(PCy3) (R = Ph (9), Cy (10), CO2Me (11), SiMe3 (12)), and Ir(C2Ph)-(CO)2(PCy3) (13) is described. The complexes 2-4 and 6 react with HSnR′3 in a 1:2 molar ratio to give IrH2(SnR′3)(TFB)(PCy3) (R′ = Ph (14), nBu (15)) and RXSnR′3 (X = O, S). The structure of 14 was determined by an X-ray investigation. Compound 14 crystallizes in the space group P1 (No. 2) with a = 10.923(1) A?, b = 10.943(1) A?, c = 19.679(1) A?, α = 75.076(5)°, β = 77.504(5)°, γ = 72.606(5)°, and Z = 2. The coordination geometry around the iridium atom could be rationalized as being derived from a highly distorted octahedron with the triphenylstannyl group and the tricyclohexylphosphine ligand occupying pseudo-trans positions (Sn-Ir-P = 129.46(3)°). In solution 14 and 15 are fluxional. The fluxional process, with values for ΔH? of 13.4 ± 0.9 (14) and 12.7 ± 0.7 (15) kcal/mol and for ΔS? of 3.0 ± 3.0 (14) and -1.6 ± 2.0 (15) eu, involves the relative positions of the diolefin atoms. The alkynyl derivative 9 reacts with HSnR′3 to afford IrH(C2Ph)(SnR′3)(TFB)(PCy3) (R′ = Ph (19), nBu (20)). Under carbon monoxide atmosphere, 19 leads to IrH(C2Ph)(SnPh3)(CO)2(PCy3) (21) and tetrafluorobenzobarrelene. Compound 21, and the related derivative IrH(C2Ph)(SnnBu3)-(CO)2(PCy 3) (22) can be also obtained by oxidative addition of the corresponding stannanes to 13. The complexes 14, 19, and 21 catalyze the addition of HSnPh3 to phenylacetylene, and from all experiments cis-PhCH=CH(SnPh3) and trans-PhCH=CH(SnPh3) were obtained.

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