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Ti3O(SC6H5)3Cl4(CH3CN)5*CH3CN*(C2H5)2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

287957-78-2

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287957-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287957-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,9,5 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 287957-78:
(8*2)+(7*8)+(6*7)+(5*9)+(4*5)+(3*7)+(2*7)+(1*8)=222
222 % 10 = 2
So 287957-78-2 is a valid CAS Registry Number.

287957-78-2Downstream Products

287957-78-2Relevant academic research and scientific papers

The synthesis and structural characterization of [Et4N]2[Ti(SPh)6] and trimeric [Ti3O(SPh)3Cl4(CH3CN)5] · CH3CN · (C2H5)2O complexes

Kim, Jun Tae,Park, Jung Woo,Koo, Sang Man

, p. 1139 - 1143 (2008/10/08)

The reaction of TiCl4 with 6 equiv. of NaSPh in the presence of organic cations such as Et4N+ or PPh4+ proceeds to yield a novel homoleptic arylthiolate Ti(IV) complex, [Ti(SPh)6]2-. The Et4N salt of [Ti(SPh)6]2- has been structurally determined. The coordination geometry around the metal ion is a regular octahedron in which the central titanium ion is located on the crystallographic inversion center. The infrared (IR) spectrum of compound I exhibits the characteristic Ti-S bond stretching vibrations of thiophenolate ligands at 480 and 430 cm-1, and the 1H NMR spectrum in CD3CN displays characteristic Et4N+ resonance peaks and six thiophenolate resonance peaks which are consistent with the solid state structure. The reaction of TiCl4 with 3 or 4 equiv. of NaSPh in CH3CN yields the unexpected mixture of dark purple [TiCl3(CH3CN)3] and dark red [Ti3O(SPh)3Cl4(CH3CN)5] · CH3CN · (C2H5)2O (II) complexes. Complex II has been structurally determined by single X-ray crystallography. The IR spectrum of complex II exhibits a μ3-O stretching vibration at 600 cm-1 and Ti-S vibrations of the thiophenolate ligand at 481 and 429 cm-1. (C) 2000 Elsevier Science Ltd.

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