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Vanadium complexes isocyanides

There are scattered reports on isocyanide complexes of other metals including copper and gold, vanadium, and several lanthanides and actinides. [Pg.80]

The complex C5H5V(CO)3CNH arises from protonation of [C5H5V-(CO)jCN] (56). This is the only vanadium isocyanide complex known. [Pg.80]

Insertions of isocyanide into niobium-carbon bonds follow a path similar to that with vanadium, resulting in the formation of the 7]2-iminoacyl complexes, which can then be involved in further chemistry.175 176 The reaction of acetone with cyclopentadienyl complex 110 under a carbon monoxide atmosphere gives the if -acetone compound 111. Complex 111 subsequently undergoes either stepwise insertion of two isocyanides via 112 or double insertion of the isocyanide to give complex 113 (Scheme 48).177... [Pg.427]

The striking advance since 1973 has been the synthesis of homoleptic isocyanides for vanadium and almost all of the post-group-VIA metals up to group IB (see Table I), and this has been helped in some respects by synthetic rationale. For example, the discovery of the simple reductive or nonreduc-tive cleavage of multiple metal-metal bonds in suitable dinuclear complexes of molybdenum and tungsten has provided a high yield route to W(CNPh)6 and [M(CNR)7]2+ (M = Mo, W) and related complexes (5-14). During these studies the series [M(CNR)7]2+ was completed with the isola-... [Pg.210]

No homoleptic isocyanide complexes of niobium, tantalum, titanium, zirconium, and halfnium have yet been synthesized. The vanadium cation... [Pg.220]

Since the vanadium center of vanadocenes is electron-deficient, various vanadium derivatives are formed by the attack with PR3, CO, or unsaturated tt-donating hgands/ This reaction provides a useful synthetic method for the synthesis of jj -alkene complexes as described later. Thus formed Cp 2V(CO) (22) is converted to the cyano derivative (23, see Cyanide Complexes of the Transition Metals) on treatment with the isocyanide (Scheme 12). ( -C5Me5)2V is incubated with O2 at -78 °C to yield [(/u.-)] -C5Me503)V(0)]2 via oxygen insertion into the carbon-vanadium bond." ... [Pg.5044]

Ishida Y, Kawaguchi H. Nitrogen atom transfer from a dinitrogen-derived vanadium nitride complex to carbon monoxide and isocyanide. J Am Chem Soc. 2014 136 16990-16993. [Pg.365]


See other pages where Vanadium complexes isocyanides is mentioned: [Pg.212]    [Pg.417]    [Pg.417]    [Pg.170]    [Pg.244]    [Pg.244]    [Pg.52]    [Pg.31]    [Pg.44]    [Pg.116]    [Pg.154]    [Pg.2578]    [Pg.5051]    [Pg.5054]    [Pg.222]    [Pg.252]    [Pg.253]    [Pg.2577]    [Pg.5050]    [Pg.5053]    [Pg.3311]    [Pg.170]    [Pg.52]    [Pg.172]    [Pg.622]    [Pg.626]    [Pg.171]    [Pg.28]   
See also in sourсe #XX -- [ Pg.462 , Pg.474 ]

See also in sourсe #XX -- [ Pg.220 , Pg.229 , Pg.231 , Pg.243 ]

See also in sourсe #XX -- [ Pg.3 , Pg.462 , Pg.474 ]




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Isocyanide complexes

Isocyanides complexes

Vanadium complexes

Vanadium complexes isocyanide

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