Dppm-substituted ruthenium clusters with capping sulfido and selenido ligands derived from thiourea, tetramethylthiourea and elemental selenium
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摘要
Treatment of [Ru3(CO)10(μ-dppm)] (4) [dppm = bis(diphenylphosphido)methane] with tetramethylthiourea at 66 °C gave the previously reported dihydrido triruthenium cluster [Ru3(μ-H)23-S)(CO)7(μ-dppm)] (5) and the new compounds [Ru33-S)2(CO)7(μ-dppm)] (6), [Ru33-S)(CO)73-CO)(μ-dppm)] (7) and [Ru33-S){η1-C(NMe2)2}(CO)63-CO)(μ-dppm)] (8) in 6%, 10%, 32%and 9%yields, respectively. Treatment of 4 with thiourea at the same temperature gave 5 and 7 in 30%and 10%yields, respectively. Compound 7 reacts further with tetramethylthiourea at 66 °C to yield 6 (30%) and a new compound [Ru33-S)21-C(NMe2)2}(CO)6(μ-dppm)] (9) (8%). Thermolysis of 8 in refluxing THF yields 7 in 55%yield. The reaction of 4 with selenium at 66 °C yields the new compounds [Ru33-Se)(CO)73-CO)(μ-dppm)] (10) and [Ru33-Se)(μ33-PhPCH2PPh(C6H4)}(CO)6(μ-CO)] (11) and the known compounds [Ru3(μ-H)23-Se)(CO)7(μ-dppm)] (12) and [Ru43-Se)4(CO)10(μ-dppm)] (13) in 29%, 5%, 2%and 5%yields, respectively. Treatment of 10 with tetramethylthiourea at 66 °C gives the mixed sulfur-selenium compounds [Ru33-S)(μ3-Se)(CO)7(μ-dppm)] (14) and [Ru33-S)(μ3-Se){η1-C(NMe2)2}(CO)6(μ-dppm)] (15) in 38%and 10%yields, respectively. The single-crystal XRD structures of 6, 7, 8, 10, 14 and 15 are reported.

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