Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆

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Chemical Name:Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆
CAS No.:1338579-22-8
Molecular Formula:C₄₄H₃₉Au₂P₂S*F₆Sb
Molecular Weight:1291.48
Hs Code.:

Au<sub>2</sub>(P(C<sub>6</sub>H<sub>5</sub>)3)2(SCH<sub>2</sub>CH<sub>2</sub>C<sub>6</sub>H<sub>5</sub>)<sup>(1+)</sup>*SbF<sub>6</sub><sup>(1-)</sup>=Au<sub>2</sub>(P(C<sub>6</sub>H<sub>5</sub>)3)2(SC<sub>2</sub>H<sub>4</sub>C<sub>6</sub>H<sub>5</sub>)SbF<sub>6</sub>

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Chemical Property of Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆

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Technology Process of Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆

There total 1 articles about Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆ 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:

: 16925-25-0
sodium hexafluoroantimonate

: 4410-99-5
2-mercaptophenylethane

: gold(III) tetrachloride trihydrate

: 603-35-0
triphenylphosphine

: 1338579-22-8
Au₂(P(C₆H₅)3)2(SCH₂CH₂C₆H₅)⁽¹⁺⁾*SbF₆^(1-)=Au₂(P(C₆H₅)3)2(SC₂H₄C₆H₅)SbF₆

: 17Au*8Au⁽¹⁺⁾*10P(C₆H₅)3*5SC₂H₄C₆H₅^(1-)*2Cl^(1-)*SbF₆^(1-)=Au₂₅(P(C₆H₅)3)10(SC₂H₄C₆H₅)5Cl₂SbF₆

Guidance literature:: With tetraoctylammonium bromide; NaBH₄; In dichloromethane; HAuCl4*3H2O in water and (C8H17)4NBr in toluene were stirred for 15 min,PPh3 in thenaol was added to toluene soln., NaBH4 in ethanol was added, 2 h at room temp. in air, rotary evapd., C6H5C2H4SH in CH2Cl2 was added , stirred for 12 h at room temp.; rotary evapd., washed with hexane, extd. with ethanol, NaSbF6 in CH2Cl2 was added for 15 min, centrifuged, dried, redissolved in CH2Cl2/ethanol (1:1), 1-2 days;
DOI:10.1021/ic2012292