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Cyclooctatetraene complexes tungsten

Another example concerns the initial electronic reduction of a-nitrostilbene (Todres et al. 1982, 1985, Todres and Tsvetkova 1987, Kraiya et al. 2004). The reduction develops according to direction a in Scheme 2.9 if the mercury cathode as well as cyclooctatetraene dianion are electron sources and according to direction b if the same stilbene enters the charge-transfer complexes with bis(pyridine)-tungsten tetra(carbonyl) or uranocene. For direction b, the charge-transfer bands in the electronic spectra are fixed. So the mentioned data reveal a great difference in electrochemical and chemical reduction processes a and b as they are marked in Scheme 2.9. [Pg.98]

Klavetter and Grubbs presented a versatile and convenient route to polyacetylene films by condensed-phase metathesis polymerization of 1,3,5,7-cyclooctatetraene, using the tungsten-based complexes 3 and 4. ... [Pg.954]


See other pages where Cyclooctatetraene complexes tungsten is mentioned: [Pg.69]    [Pg.7]    [Pg.355]    [Pg.355]    [Pg.343]    [Pg.380]    [Pg.21]    [Pg.398]    [Pg.16]    [Pg.114]    [Pg.114]   
See also in sourсe #XX -- [ Pg.380 ]




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