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Polyborane carbonyls

Polyborane carbonyls with B—C attachments are prepared by displacement " ... [Pg.183]

Diborane is not unique among the boron hydrides in its ability to form a carbonyl. High pressure reaction of either pentaborane-f / or tetra-borane-10 with carbon monoxide forms a substance which behaves like borane-carbonyl in its manner of decomposition. The formula of this polyborane-carbonyl has recently been established as OC B Hg (mp, — 114.5° bp, 59.6°) 41a). It reacts with trimethylamine without release of carbon monoxide. [Pg.301]

Fig. 13. The stmctures of closo metallaboranes where O represents BH , CH (a) [< /(9j 0-( q -C H )Ni(B22H22)] (b) closo-l]l-[v[-Q ]) -l]l-53i] pri Closo metallaboranes can also be formed by the direct interaction of polyborane and metal carbonyl clusters. For example. Fig. 13. The stmctures of closo metallaboranes where O represents BH , CH (a) [< /(9j 0-( q -C H )Ni(B22H22)] (b) closo-l]l-[v[-Q ]) -l]l-53i] pri Closo metallaboranes can also be formed by the direct interaction of polyborane and metal carbonyl clusters. For example.
Closo metallaboranes can also he formed by the direct interaction of polyborane and metal carbonyl clusters. For example,... [Pg.243]

Recently, Wade has pointed out a formal analogy between the electronic structures of carboranes and polyboranes and those of metal carbonyl clusters based on the assumption that certain triangulated polyhedra require the same number of skeletal orbitals whether there are BH or CH units as well as transition metal atoms at their apices (120). This assumption is quite reasonable as the synthesis of a large number of polyboranes and carboranes in which a transition metal atom takes the place of a BH skeletal unit may be carried out (70). [Pg.337]


See other pages where Polyborane carbonyls is mentioned: [Pg.232]    [Pg.232]    [Pg.160]    [Pg.68]   


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