作者: Robert E. Stevens , Douglas E. Fjare , Wayne L. Gladfelter
DOI: 10.1016/0022-328X(88)80161-X
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摘要: Abstract Decarbonylnitrosyltriruthenate, [Ru3(CO)10(NO)]−, exhibits reactivity at both the nitrosyl ligand and metal core. The NO bond can be cleaved in a thermal reaction to give [Ru5N(CO)14]− low yield, whereas [Ru3(NCO)(CO)11]− formed quantitatively when [Ru3(CO)10(NO)]− is photolyzed under CO. carbonyl ligands of cluster are readily substituted by triphenylphosphine trimethylphosphite giving [Ru3(CO)9L(NO)]− (where L = PPh3, P(OCH3)3). Under an atmosphere 13CO complete exchange with observed. clusters have been characterized infrared NMR spectroscopies as well their reactions acids HRu3(CO)9L(NO). With anionic nucleophile, PPN(NO2), photochemically reacts CO form [Ru(CO)3NO)]−. This new carbonylmetalate also prepared from PPN (NO2) Ru(CO)5.