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[Ni(P(o-C6H3-3-SiMe3-2-S)2(o-C6H3-3-SiMe3-2-SH))]2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

956107-45-2

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956107-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956107-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,1,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 956107-45:
(8*9)+(7*5)+(6*6)+(5*1)+(4*0)+(3*7)+(2*4)+(1*5)=182
182 % 10 = 2
So 956107-45-2 is a valid CAS Registry Number.

956107-45-2Relevant academic research and scientific papers

Mononuclear Ni(II)-thiolate complexes with pendant thiol and dinuclear Ni(III/II)-thiolate complexes with Ni...Ni interaction regulated by the oxidation levels of nickels and the coordinated ligands

Lee, Chien-Ming,Chiou, Tzung-Wen,Chen, Hsin-Hung,Chiang, Chao-Yi,Kuo, Ting-Shen,Liaw, Wen-Feng

, p. 8913 - 8923 (2008/10/09)

Compared to [NiII(SePh)(P(o-C6H3-3- SiMe3-2-S)2(o-C6H3-3-SiMe 3-2-SH))]- (1a) and [NiII(Cl)(P(o-C 6H3-3-SiMe3-2-S)2-(o-C 6H3-3-SiMe3-2-SH))]- (3a) with a combination of the intramolecular [Ni...H-S] and [Ni-S...H-S] interactions, complexes [NiII(SePh)(P(o-C6H 3-3-SiMe3-2-S)2(o-C6H 3-3-SiMe3-2-SH))]- (1b) and [Ni II(Cl)(P (o-C6H3-3-SiMe3-2-S) 2-(o-C6H3-3-SiMe3-2-SH))] - (3b) with intramolecular [Ni...H-S] interaction exhibit lower νS-H stretching frequencies (2137 and 2235 cm-1 for 1b and 3b vs 2250 and 2287 cm-1 for 1a and 3a, respectively) and smaller torsion angles (27.2° for 3b vs 58.9 and 59.1° for 1a and 3a, respectively). The pendant thiol interaction modes of 1a, 3a, and 3b in the solid state are controlled by the solvent pairs of crystallization. Oxygen oxidation of dinuclear [NiII-(P(o-C6H3-3- SiMe3-2-S)2(o-C6H3-3-SiMe 3-2-SH))]2 (4) yielded thermally stable dinuclear [Ni III(P(o-C6H3-3-SiMe3-2-S) 2(o-C6H3-3-SiMe3-2-μ-S))] 2 (5). The two paramagnetic d7 NiIII cores (S = 1/2) with antiferromagnetic coupling (J = -3.13 cm-1) rationalize the diamagnetic property of 5. The fully delocalized mixed-valence [Ni(II)-Ni(III)] complexes [Ni2(P(o-C6H 3-3-SiMe3-2-S)3)2]- (6) and [Ni2(P(o-C6H3-3-SiMe3-2-S) 3)(P(o-C6H3-3-SiMe3-2-S) 2(o-C6H3-3-SiMe3-2-SCH 3))] (7) were isolated upon the reduction of 5 and the methylation of 6, respectively. The electronic perturbation from the sulfur methylation of 6 triggers the stronger Ni...Ni interaction and the geometrical rearrangement from the diamond shape of the [NiS2Ni] core to the butterfly structure of [Ni(μ-S)2Ni] to yield 7 with Ni...Ni distances of 2.6088(1) A. The distinctly different Ni...Ni distances (2.6026(7) for 5 and 2.8289(15) A for 6) and the coordination number of the nickels indicate a balance of geometrical requirements for different oxidation levels of [PS3Ni-NiPS3] cores of 5 and 6.

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