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Closo-decaborate

Both electrolytic and protolytic methods of decomposition of iodo-benzenenonahydro-closo-decaborate(l—), B,0H9IPh, led to the formation of B10H9T. 52... [Pg.104]

C12H3 8B14C0N, Tetraethylammonium 2,2 -commo-bis(nonahydrodicarba-2-cobalta-closo-decaborate), 38B, 639 C12H40B18N2Ni, N,N -Dimethyltriethylenediammonium bis-(3)-1,2-dicar-bollylnickelate, 35B, 431... [Pg.312]

However, the chemistry of c/oi o-decaborate is much less studied than the c/oio-dodecaborate chemistry. The carba-c/oio-dodecaborate anion [CB,H,2] combines advantages of both its iso-structural and isoelectronic analogs, [C2B10H12] and [B,2H,2] the good solubility in water as the sodium salt and the presence of carbon atom available for functionalization using standard methods of organic chemistry [20], It should be noted that the practical importance of the cwha-closo-dodecaborate anion was very limited up to recently when convenient methods for the synthesis of the parent cluster and its C-phenyl derivatives were developed [21], A few examples of incorporation of [CBiiHi2] into various porphyrins have been reported quite recently [22],... [Pg.183]

A similar approach was applied for the synthesis of benzoic acids derived from the closo-dodecaborate [45], cZoio-decaborate [43], and cobalt bis(dicarbollide) [46,47] anions. [Pg.625]


See other pages where Closo-decaborate is mentioned: [Pg.802]    [Pg.72]    [Pg.802]    [Pg.461]    [Pg.460]    [Pg.66]    [Pg.66]    [Pg.78]    [Pg.311]    [Pg.579]    [Pg.815]    [Pg.39]    [Pg.802]    [Pg.72]    [Pg.802]    [Pg.461]    [Pg.460]    [Pg.66]    [Pg.66]    [Pg.78]    [Pg.311]    [Pg.579]    [Pg.815]    [Pg.39]    [Pg.50]    [Pg.144]    [Pg.144]    [Pg.67]    [Pg.133]    [Pg.323]    [Pg.819]   
See also in sourсe #XX -- [ Pg.2 , Pg.50 , Pg.72 , Pg.77 ]




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