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[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2](1+)*ClO4(1-)=[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2]ClO4

Base Information Edit
  • Chemical Name:[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2](1+)*ClO4(1-)=[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2]ClO4
  • CAS No.:301647-76-7
  • Molecular Formula:C75H61OP4Pt*ClO4
  • Molecular Weight:1396.73
  • Hs Code.:
  • Mol file:301647-76-7.mol
[Pt(C<sub>6</sub>H<sub>4</sub>P(C<sub>6</sub>H<sub>5</sub>)2CHCOCHP(C<sub>6</sub>H<sub>5</sub>)3)(P(C<sub>6</sub>H<sub>5</sub>)3)2]<sup>(1+)</sup>*ClO<sub>4</sub><sup>(1-)</sup>=[Pt(C<sub>6</sub>H<sub>4</sub>P(C<sub>6</sub>H<sub>5</sub>)2CHCOCHP(C<sub>6</sub>H<sub>5</sub>)3)(P(C<sub>6</sub>H<sub>5</sub>)3)2]ClO<sub>4</sub>

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Chemical Property of [Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2](1+)*ClO4(1-)=[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2]ClO4 Edit
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Technology Process of [Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2](1+)*ClO4(1-)=[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2]ClO4

There total 1 articles about [Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2](1+)*ClO4(1-)=[Pt(C6H4P(C6H5)2CHCOCHP(C6H5)3)(P(C6H5)3)2]ClO4 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:
With sodium hydride; In tetrahydrofuran; byproducts: H2, NCCH3, NaClO4; excess of P(C6H5)3 added to suspn. of Pt complex in THF, NaH (excess) added, mixt. stirred at 25°C overnight; filtered, filtrate evapd. to dryness, extd. with CH2Cl2, filtered, soln.evapd. to dryness, solid collected with Et2O, dried on air; elem. anal.;
DOI:10.1039/b002848g
Guidance literature:
In dichloromethane; byproducts: S(CH2)4; ClAuS(CH2)4 added to soln. of Pt complex in CH2Cl2, stirred at 25°C for 15 min; evapd. to dryness, residue treated with Et2O;
DOI:10.1039/b002848g
upstream raw materials:

triphenylphosphine

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