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175985-32-7

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175985-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175985-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,9,8 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175985-32:
(8*1)+(7*7)+(6*5)+(5*9)+(4*8)+(3*5)+(2*3)+(1*2)=187
187 % 10 = 7
So 175985-32-7 is a valid CAS Registry Number.

175985-32-7Downstream Products

175985-32-7Relevant articles and documents

Synthesis and Reactivity of Group 4 Homoleptic Selenolates and Tellurolates: Lewis Base Induced Conversion to Terminal and Bridging Chalcogenides

Gerlach, Christopher P.,Christou, Victor,Arnold, John

, p. 2758 - 2766 (2008/10/09)

A combination of either salt metathesis reactions between MCl4 (M = Zr, Hf) and (THF)2LiSeSi(SiMe3)3 (THF = tetrahydrofuran) or between TiCl3(THF)3 and (THF)2LiESi(SiME3)3 (E = Se, Te), or chalcogenolysis reactions between M(CH2Ph)4 (M = Zr, Hf) and HESi(SiMe3)3 (E = Se, Te) afforded the series of compounds M[ESi(SiMe3)3]4 (M = Ti, Zr, Hf; E = Se, Te). The X-ray structures of M[TeSi(SiMe3)3]4 (M = Zr, Hf) and Zr[SeSi(SiMe3)3]4 have been determined and are presented for comparison. Reaction of group 4 tetrabenzyls with 3 equiv of HSeSi(SiMe3)3 gave the complexes M[SeSi(SiMe3)3]3(CH2Ph) (M = Ti, Zr, Hf) in high yields. Treatment of the zirconium and hafnium homoleptic tellurolates with 2 equiv of xylyl isocyanide produced the bis-L trans adducts M[TeSi(SiMe3)3]4[CN(xylyl)]2 (M = Zr, Hf) in moderate yields. The related six-coordinate DMPE adducts M[TeSi(SiMe3)3]4(DMPE) (M = Zr, Hf; DMPE = 1,2-bis(dimethylphosphino)ethane) were similarly prepared. Reaction of the mono-DMPE complexes with a second equilvalent of DMPE led to the elimination of Te[Si(SiMe3)3]2 and the formation of the seven-coordinate bis(tellurolate), bis(DMPE), terminal tellurides M[TeSi(SiMe3)3]2(Te)(DMPE)2 (M = Zr, Hf). Both of the tellurides have been structurally characterized. The homoleptic zirconium selenolate reacts with 1 equiv of DMPE, yielding a bright red material with the stoichiometry Zr[SeSi(SiMe3)3]2(Se)(DMPE). The diphosphine DMPM (DMPM = 1,2-bis(dimethylphosphino)methane) also reacted with M[SeSi(SiMe3)3]4 (M = Zr, Hf) to give the bis(μ-Se), A-frame dimers {M[SeSi(SiMe3)3]2(μ-Se)(μ-η 2-DMPM)}2 (M = Zr, Hf) in relatively low yields (40 and 23percent). The structure of the zirconium derivative has been confirmed using X-ray crystallography. Crystallographic data are as follows: Zr[SeSi(SiMe3)3]4, monoclinic, P21/c, a = 22.6944(34) A?, b = 15.2943(55) A?, c = 22.7758(61) A?, β= 105.695(17)°, Z = 4, R = 5.29, Rw = 3.69; Hf[TeSi(SiMe3)3]4, monoclinic, P21/c, a = 22.494(5) A?, b = 15.609(5) A?, c = 22.742(5) A?, β= 104.480(5)°, Z = 4, R = 4.48, Rw = 5.45; Hf[TeSi(SiMe3)3]2(Te)(DMPE)2, monoclinic, P21, a = 14.795(3) A?, b = 14.289(3) A?, c = 15.4212(2) A?, β= 102.543(3)°, Z = 2, R = 4.78, Rw = 6.70; {Zr[SeSi(SiMe3)3]2(μ-Se)(μ-η 2-DMPM)}2, monoclinic, P21/n, a = 14.7651(13) A?, b = 18.8579(17) A?, c = 18.6072(17) A?, β= 111.031(1)°, Z = 2, R = 8.26, Rw = 8.13.

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