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Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5)

Base Information Edit
  • Chemical Name:Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5)
  • CAS No.:21135-20-6
  • Molecular Formula:Au*C5H5*C18H15P
  • Molecular Weight:524.352
  • Hs Code.:
  • Mol file:21135-20-6.mol
Au<sup>(1+)</sup>*P(C<sub>6</sub>H<sub>5</sub>)3*C<sub>5</sub>H<sub>5</sub><sup>(1-)</sup> = Au(P(C<sub>6</sub>H<sub>5</sub>)3)(C<sub>5</sub>H<sub>5</sub>)

Synonyms:Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5)

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Chemical Property of Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5) Edit
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Technology Process of Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5)

There total 3 articles about Au(1+)*P(C6H5)3*C5H5(1-) = Au(P(C6H5)3)(C5H5) 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 tetrahydrofuran; (Ar), a susp. of BF4-salt, NaH and C5H6 in THF stirred at 0°C for 15 min, soln. diluted with petroleum ether cooled to 0°C, filtered, poured in ice water with stirring; separated, washed with cold ethanol and ether, dried in vac.;
Guidance literature:
With Na(OC2H5); In ethanol; byproducts: NaCl, C2H5OH; sodium ethoxide and cyclopentadiene added to a suspn. of Au-compound; stirred overnight; IR, NMR;
DOI:10.1039/DT9860000411
Guidance literature:
In tetrahydrofuran; to a soln. of AuBrPPh3 in THF added soln. of NaC5H5 in THF at -35°C, after 40 min mixture heated to 0°C, poured into ice water with stirring; filtered, washed with water and cold acetone, dissolved in 4:1 acetone-THF mixture cooled to 0°C, ice water added;
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