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{((C5H5)2Ti(SCH2CH2CH2S)2Ti(C5H5)2)Ag}(1+)*B(C6H5)4(1-)={((C5H5)2Ti(SCH2CH2CH2S)2Ti(C5H5)2)Ag}B(C6H5)4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137232-45-2

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137232-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137232-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,3 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137232-45:
(8*1)+(7*3)+(6*7)+(5*2)+(4*3)+(3*2)+(2*4)+(1*5)=112
112 % 10 = 2
So 137232-45-2 is a valid CAS Registry Number.

137232-45-2Downstream Products

137232-45-2Relevant academic research and scientific papers

Redox-active macrocycles as metalloligands: Synthesis, electrochemistry, and structure of silver(I) and copper(I) complexes of Cp2Ti(μ-S(CH2)nS)2TiCp 2 (n = 2, 3)

Timothy Nadasdi,Stephan, Douglas W.

, p. 116 - 122 (2008/10/08)

The reactions of Cp2TiCl2 with the dithiols HS(CH2)nSH (n = 2, 3) in the presence of imidazole proceed with formation of imidazole hydrochloride, affording insoluble titanocene dithiolate derivatives 1 and 2, respectively. In the case of propanedithiol, the product 2 can also be synthesized via reaction of Cp2TiCl2 with Mg and (SCH2CH2CH2S)2 or by reaction of Cp2Ti(PMe3)2 with (SCH2CH2CH2S)2. Alternatively, 2 can be prepared via the reaction of Cp2TiPh2 with dithiols. The spectroscopic and analytical data are consistent with the formulation of 1 and 2 as the bimetallic compounds Cp2Ti(μ-S(CH2)nS)2TiCp 2 (n = 2, 1; n = 3, 2). The 1H NMR data suggest an open macrocyclic structure for 2. In contrast, the temperature dependence of the 1H NMR spectra for 1 is consistent with a fluxional process involving the twisted conformations of 1 in which two of the four sulfur atoms bridge the two Ti centers. Molecules 1 and 2 are shown to act as metalloligands and react with AgBPh4 and [Cu(NCMe)4]BF4 to yield the complexes [(Cp2Ti(μ-S(CH2)nS)2TiCp 2)M]+X- (n = 2, M = Cu(I), 3; n = 3, M = Ag(I), 4). A crystallography study of 4 confirms the formulation of 4 in which 2 acts as a macrocyclic metalloligand presenting a four-sulfur coordination sphere to the encapsulated silver ion. The complex [(Cp2Ti(μ-SCH2CH2CH2S) 2TiCp2)Ag]BPh4 (4) crystallizes as 4·H2O·0.75CH2Cl2 in the space group P21/n with a = 24.610 (9) A?, b = 17.098 (5) A?, c = 25.453 (15) A?, β = 111.76 (3)°, Z = 8, and V = 9947 (14) A?3. Electrochemical studies of 1-4 by cyclic voltammetry are reported. The macrocycles exhibit only irreversible reductions. In contrast, the complexes 3 and 4 undergo quasi-reversible one-electron reductions at -0.93 and -1.26 V vs Ag/AgCl, respectively. A second irreversible wave is also observed at -1.56 and -1.53 V for 3 and 4, respectively. This redox behavior is interpreted in terms of Ti(IV)/Ti(III) redox couples. The chemical generation of the one-electron-reduction products, i.e. [(Cp2Ti(μ-S(CH2)nS)2TiCp 2)M]0 (n = 2, M = Cu(I), 5; n - 3, M = Ag(I), 6) is achieved via reactions of 3 and 4 with Cp2Co. The EPR spectrum of 5 reveals 63Cu, 65Cu hyperfine coupling, while 107Ag, 109Ag hyperfine coupling is seen for 6. The results of these studies are discussed, and the implications of the data are considered.

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