dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

Base Information

Chemical Name:dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)
CAS No.:150392-41-9
Molecular Formula:C₄₁H₄₁Cl₂NP₂Ru
Molecular Weight:781.707
Hs Code.:

Synonyms:dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

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Chemical Property of dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

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Technology Process of dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

There total 1 articles about dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II) 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:

Reference yield:

: 1426385-01-4
C₄₁H₄₃Cl₂NOP₂Ru

: 150392-41-9
dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

Guidance literature:: at 80 ℃; Inert atmosphere;
DOI:10.1039/c3dt32909g

Reference yield: 100.0%

: 150392-41-9
dichloro(o-diphenylphosphino-N,N-dimethylaniline)(tris(p-tolyl)phosphine)ruthenium(II)

: 201230-82-2
carbon monoxide

: trans-RuCl2(o-diphenylphosphino-N,N’-dimethylaniline)(P(p-tolyl)3)(CO)

Guidance literature:: In neat (no solvent); at 22 ℃; for 6h; Solvent; Schlenk technique; Inert atmosphere;
DOI:10.1039/c3dt51625c

Reference yield: 100.0%

: 150392-41-9
RuCl₂(o-(diphenylphosphino)-N,N-dimethylaniline)(P(p-tolyl)3)

: 7783-06-4
hydrogen sulfide

: RuCl₂(o-(diphenylphosphino)-N,N-dimethylaniline)(P(p-tolyl)3)(SH₂)

Guidance literature:: In neat (no solvent); absence of air and moisture; stirring under 1 atm H2S at 20°C for2 h; addn. of hexanes, stirring for 15 min, collection (filtration), drying (;
DOI:10.1021/ic9707772