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[Ir(2-triphenylsilylbenzenethiolate)(CO)(PPh3)2] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170472-37-4

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170472-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170472-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,4,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 170472-37:
(8*1)+(7*7)+(6*0)+(5*4)+(4*7)+(3*2)+(2*3)+(1*7)=124
124 % 10 = 4
So 170472-37-4 is a valid CAS Registry Number.

170472-37-4Downstream Products

170472-37-4Relevant academic research and scientific papers

Synthesis of Complexes of Re(V), Ru(II), Os(II), Rh(I), Ir(I) and Ir(III). Crystal and Molecular Structures of , and

Ahmet, Mustafa T.,Lu, Canzhong,Dilworth, Jonathan R.,Miller, John R.,Zheng, Yifan,et al.

, p. 3143 - 3152 (1995)

The rhenium(V) precursors (X = Cl or Br) reacted with 2-triphenylsilylbenzenethiol in methanol in the presence of base to give 1 and 2 respectively.In the presence of NaBH4 and no base the blue thiolate polyhydride 3 was formed in high yield.The crystal structures of 2 and 3 were determined and showed 2 to be monomeric with distorted trigonal-bipyramidal geometry and the oxide and hydroxide ligands in equatorial sites.The thiolate and phosphine ligands of 3 are in a tetrahedral array with the hydride ligands assumed to be in capping sites on the tetrahedral faces.Reaction of the thiol with in methanol in the presence of NEt3 gave 4 in good yield.Its crystal structure revealed the geometry about the Ir to be pseudo-octahedral with mer phosphine ligands and cis thiolates, and the hydride presumed to be in a vacant site trans to a thiolate ligand.The complex reacted under similar conditions to give monomeric 6 whereas gave 5; gave 7 whereas formed 8.The potentially bidentate thiol SiPh2(C6H4SH-2)2 gave a series of products with the same precursors which proved difficult to characterise unequivocally in the absence of X-ray structural data.The geometry adopted by the SC6H4SiPh3-2 ligand was analysed in some detail and contrasted with symmetrically 2,6-disubstituted aromatic thiolates.

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