Osmium carbonyl clusters with alkynes

Heterometal alkoxide precursors, for ceramics, 12, 60-61 Heterometal chalcogenides, synthesis, 12, 62 Heterometal cubanes, as metal-organic precursor, 12, 39 Heterometallic alkenes, with platinum, 8, 639 Heterometallic alkynes, with platinum, models, 8, 650 Heterometallic clusters as heterogeneous catalyst precursors, 12, 767 in homogeneous catalysis, 12, 761 with Ni—M and Ni-C cr-bonded complexes, 8, 115 Heterometallic complexes with arene chromium carbonyls, 5, 259 bridged chromium isonitriles, 5, 274 with cyclopentadienyl hydride niobium moieties, 5, 72 with ruthenium—osmium, overview, 6, 1045—1116 with tungsten carbonyls, 5, 702 Heterometallic dimers, palladium complexes, 8, 210 Heterometallic iron-containing compounds cluster compounds, 6, 331 dinuclear compounds, 6, 319 overview, 6, 319-352... 

Alkynes containing methylene (—CHi—) functionalities a to the triple bond readily undergo thermal C-H activation under conditions necessary to initiate reaction with group VIII metal carbonyls (54). The allenyl clusters obtained isomerize thermally via a 1,2-hydrogen atom shift to afford the thermodynamically more favorable 1,3-dimetalloallyl clusters (Table 1) (49,55). A similar chemistry has been recognized for osmium clusters, albeit under more severe conditions. 

Reactions of ruthenium and osmium cluster carbonyls with heteroatom-substituted and functionalized alkynes (metallocycles) 00IZV1. 

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