Synthesis of the mixed-metal clusters [Ru5RhC(CO)14(cod)Y][Y = H, Au(PEt3) or Au(PPh3); cod = cycloocta-1,5-diene]; reactions of [Ru5RhC(CO)14(cod){Au(PR3)}](R = Ph or Et) and crystal structure of [Ru5RhC(CO)14(cod){µ3-Au(PPh3)}]

Synthesis of the mixed-metal clusters [Ru5RhC(CO)14(cod)Y][Y = H, Au(PEt3) or Au(PPh3); cod = cycloocta-1,5-diene]; reactions of [Ru5RhC(CO)14(cod){Au(PR3)}](R = Ph or Et) and crystal structure of [Ru5RhC(CO)14(cod){µ3-Au(PPh3)}]
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[Ru5RhC(CO)14(cod)Y][Y = H, Au(PEt3) 或 Au(PPh3) 的合成; cod = cycloocta-1,5-diene] 反应; )14(cod){Au(PR3)}](R = Ph 或 Et) 和 [Ru5RhC(CO)14(cod){µ3-Au(PPh3)}] 的晶体结构

DOI:
10.1039/dt9940003069
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发表时间:
1994
期刊:
Journal of The Chemical Society-dalton Transactions
影响因子:
--
通讯作者:
Jill Morris
Jill Morris
中科院分区:
--
文献类型:
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作者:
T. Adatia;H. Curtis;B. Johnson;Jack Lewis;M. Mcpartlin;Jill Morris

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用过量的[Rh(Cod)2][SbF 6](cod =环辛-1,5-二烯)处理五钌盐[N(PPh 3)2]2[Ru 5C(CO)14],得到单阴离子[Ru 5 RhC(CO)14(cod)]-,其分离为[N(PPh 3)2]+盐1。一价阴离子与HBF_4·Et_2O反应,生成配体[Ru_5RhH(C)(CO)_(14)(cod)]_2。化合物1分别与金盐[Au(PPh 3)]Cl和[Au(PEt 3)]Cl反应,得到簇合物[Ru 5 RhC(CO)14(cod){Au(PPh 3)}]3和[Ru 5 RhC(CO)14(cod){Au(PEt 3)}]4。化合物3的晶体属于三斜晶系空间群P(no.2),a= 15.993(3),B= 9.728(2),c= 13.900(3)A,α= 90.29(2),β= 99.97(2),γ= 88.36(2)°。金属核几何结构由中心Ru 5 Rh八面体组成,其中一个Ru 3面被µ3-Au(PPh 3)片段覆盖[Ru-Ru 2.787(1)-3.093(1); Ru-Rh 2.892(1)-2.952(1); Ru-Au 2.735(1)-3.082(1)A]。报道了化合物3和4与降冰片二烯、PPh_3和P(OMe)_3的反应。
Treatment of the pentaruthenium salt [N(PPh3)2]2[Ru5C(CO)14] with an excess of [Rh(Cod)2][SbF6](cod = cycloocta-1,5-diene) yielded the monoanion [Ru5RhC(CO)14(cod)]– which has been isolated as its [N(PPh3)2]+ salt 1. Reaction of the monoanion with HBF4·Et2O gave the hydrido derivative [Ru5RhH(C)(CO)14(cod)]2. Compound 1 reacted with the gold salts [Au(PPh3)]Cl and [Au(PEt3)]Cl, respectively, to yield the cluster compounds [Ru5RhC(CO)14(cod){Au(PPh3)}]3 and [Ru5RhC(CO)14(cod){Au(PEt3)}]4. Compound 3 crystallises in the triclinic space group P(no. 2) with a= 15.993(3), b= 9.728(2), c= 13.900(3)A, α= 90.29(2), β= 99.97(2), γ= 88.36(2)°. The metal core geometry consists of a central Ru5Rh octahedron with one Ru3 face capped by a µ3-Au(PPh3) fragment [Ru–Ru 2.787(1)–3.093(1); Ru–Rh 2.892(1)–2.952(1); Ru–Au 2.735(1)–3.082(1)A]. The reactions of 3 and 4 with norbornadiene, PPh3 and P(OMe)3 are reported.