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Ir(H)C6H3(CH3)2(P(C4H9)2O)2C6H2F is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

686274-29-3

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686274-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 686274-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,6,2,7 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 686274-29:
(8*6)+(7*8)+(6*6)+(5*2)+(4*7)+(3*4)+(2*2)+(1*9)=203
203 % 10 = 3
So 686274-29-3 is a valid CAS Registry Number.

686274-29-3Downstream Products

686274-29-3Relevant academic research and scientific papers

Synthesis and Properties of Iridium Bis(phosphinite) Pincer Complexes (p-XPCP)IrH2, (p-XPCP)Ir(CO), (p-XPCP)Ir(H)(aryl), and {(p-XPCP)Ir}H2{μ-N2} and Their Relevance in Alkane Transfer Dehydrogenation

Goettker-Schnetmann, Inigo,White, Peter S.,Brookhart, Maurice

, p. 1766 - 1776 (2008/10/09)

A series of bis(phosphinite) (p-XPCP)IrH2 pincer complexes {[PCP = η3-5-X-C6H2[OP-(tBu)2] 2-1,3], X = MeO (6a), Me (6b), H (6c), P (6d), C6F 5 (6e), and ArF [=3,5-bis-(trifluoromethyl)phenyl] (6f)} have been synthesized by dehydrochlorination of (p-XPCP)-IrHCl precursor complexes 4a-f with NaOtBu in the presence of hydrogen. Dehydrochlorination of 4f in the presence of nitrogen yields {(p-ArFPCP)Ir} 2{μ-N2} (11f), which was analyzed by X-ray diffraction. Complexes 6a-f exhibit identical catalytic activity in the transfer dehydrogenation of cyclooctane (COA) with tert-butylethylene (TBE) when compared to mixtures of precatalysts 4a-f and NaOtBu. The electronic properties of the fragments (p-XPCP)Ir (Aa-f) are discussed on the basis of the vCO of (p-XPCP)Ir(CO) complexes (8a-f) as well as on VHD coupling constants of monodeuterated complexes (p-XPCP)IrHD (6a-f-d1). Reaction of 4a-f with NaOtBu in arene solvents generates (p-XPCP)Ir(aryD(H) complexes (9 and 10), which undergo rapid arene exchange on the NMR time scale. Exchange rates are zero-order in free arene, implying a dissociative exchange mechanism. More electron-deficient complexes, e.g., (p-C6F5PCP)Ir(m-xylyl) (H) (10e) or (p-ArFPCP)Ir(m-xylyl)(H) (10f), reductively eliminate m-xylene significantly faster than the more electron-rich complexes, e.g., (p-MeOPCP)Ir(m-xylyD(H) (10a), on the basis of the line widths δv 1/2(0°C) of the hydridic NMR resonances of (p-XPCP)Ir(m-xylyl)(H) complexes 10a-f. The same correlation with substituent effects applies to the catalytic activity (initial turnover frequencies) of complexes 6a-f in the transfer dehydrogenation of COA with TBE.

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