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trans-(trichlorostannato)bis(triethylphosphine)phenylplatinum(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15170-02-2

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15170-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15170-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,7 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15170-02:
(7*1)+(6*5)+(5*1)+(4*7)+(3*0)+(2*0)+(1*2)=72
72 % 10 = 2
So 15170-02-2 is a valid CAS Registry Number.

15170-02-2Downstream Products

15170-02-2Relevant academic research and scientific papers

195Pt, 119Sn AND 31P NMR STUDIES OF ALKYL, ARYL AND ACYL TRICHLOROSTANNATE COMPLEXES OF PLATINUM(II). THE CRYSTAL STRUCTURE OF trans-

Albinati, Alberto,Gunten, Urs von,Pregosin, Paul S.,Ruegg, Hubert J.

, p. 239 - 256 (2007/10/02)

195Pt, 119Sn and 31P NMR characteristics of the complexes tans-).The values of 1J(195Pt, 119Sn) vary from 2376 to 11895 Hz with the COPh ligand having the smallest and the C6H5 ligand the largest value, making a total range for this coupling constant, when the dimer syn-trans-2 is includeed, of ca. 33000 Hz.In the meta- and para-substituted phenyl complexes 1J(195Pt, 119Sn) (a) is greater for electron withdrawing substituents, (b) varies more for the meta-substituted derivatives (5634 to 7906 Hz) than for the para analogues (6088 to 7644 Hz) and (c) has the lowest values when the group is the meta- or para-substituent.The direction of the change in 1J(195Pt, 119Sn) is opposite to that found for 1J(195Pt, 31P).For the aryl complexes linear correlations are observed between δ(119Sn),1J(195Pt, 119Sn), 1J(195Pt, 31P), 2J(119Sn, 31P) and the Hamett substituent consatnt ?n. δ(119Sn) and 1J(195Pt,119Sn) are related linearly to ν(Pt-H) in the complexes trans-; δ(119Sn) and δ(1H) (hydride) are also linearly related.Based on 1J(195Pt,119Sn), the acyl ligand is suggested to have a very large NMR trans influence.The differences in the NMR parameters for (1a-e) are rationalized in terms of differing ?- and ?-bonding abilities of the carbon ligands.The structure of 1c has been determined by crystallographic methods.The complex has a slightly distorted square planar geomety with trans-PEt3 ligands.Relevant bond lengths (Angstroem) and bond angles (deg) are: Pt-Sn, 2.634(1), Pt-P, 2.324(4) and 2,329(4), Pt-C, 2.05(1); P-Pt-P, 170.7(6), Sn-Pt-C, 173.0(3), Sn-Pt-P, 92.1(19, 91.7(1), P-Pt-C, 88.8(4) and 88.3(4).The Pt-Sn bond separation is the longest yet observed for square-planar platinum trichlorostannate complexes, and would be consistent with a large crystallographic trans influence of the benzoyl ligand.The Pt-Sn bond separation is shown to correlate with 1J(195Pt, 119Sn).

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