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(cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate

Base Information
  • Chemical Name:(cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate
  • CAS No.:94904-42-4
  • Molecular Formula:C30H30P2PtS2*2F6P
  • Molecular Weight:1001.66
  • Hs Code.:
(cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate

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Chemical Property of (cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate
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Technology Process of (cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate

There total 2 articles about (cis-6,17-diphenyl-6,17-diphospha-2,13-dithiatricyclo{16.4.0.0(7.12)}docosa-7(12),8,10,1(18),19,21-hexaene-κ(2)S,κ(2)P)platinum(II) dihexafluorophosphate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In ethanol; dichloromethane; addn. of (1,5-cyclooctadiene) platinum(II) dichloride to a stirred soln. of phosphino-ligand in CH2Cl2, treating with 95% EtOH to give a clear soln., addn. of PF6(1-)-salt in EtOH, stirring for 2 h; filtration, concg., recrystn. (MeCN/C6H6), elem. anal.;
Guidance literature:
In ethanol; dichloromethane; AgPF6 is added to a soln. of macrocycle and (1,5-cyclooctadiene)PtCl2 in ethanol and CH2Cl2; concn. and extn. with MeCN, filtn. through celite and concn., resulting solid is recrystd. from MeCN/benzene, then dried at 80°C for 1 h under high vac., elem. anal.;
DOI:10.1021/ja00293a052
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