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1.4- Diynes special

A subsidiary approach involves nuclear modification of the arylsilanes so obtained. The requisite organometallics can be prepared from aryl halides, or by deprotonation of a suitably activated (c.g. methoxy-substituted) arene. A more specialized route involves cycloaddition between alkynylsilanes and diynes. [Pg.114]

Special cases are 39 and 41 in which two diyne moieties are separated by a bicyclic framework. In both compounds the sharp and easily recognizable PE bands of the triple bonds can be used to investigate long-range interactions. In 39 the interaction between both acetylenic moieties was found to be small i. In 41, however, a splitting of 0.5 eV has been detected (see Figure 10). It has been traced back to a strong interaction between the valence orbitals of the bicyclo[l. 1. Ijpentane moiety and the tt-MOs of the triple bonds . ... [Pg.163]


See other pages where 1.4- Diynes special is mentioned: [Pg.89]    [Pg.368]    [Pg.368]    [Pg.357]    [Pg.374]    [Pg.994]    [Pg.464]    [Pg.21]    [Pg.228]    [Pg.54]    [Pg.267]    [Pg.206]    [Pg.2184]    [Pg.149]    [Pg.228]    [Pg.91]    [Pg.246]    [Pg.232]    [Pg.283]    [Pg.222]    [Pg.54]    [Pg.234]    [Pg.237]    [Pg.348]   


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Diynes

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