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Cyano compounds geometry

Starting from the assumption that the geometry relaxation after excitation is of primary importance with respect to the luminescence response, we decided to employ a solid polymer matrix to suppress conformational changes of the oligomers. For the measurements, dilute blends with polysulfone as the transparent host matrix were prepared. In Figure 16-13, the PL decay curves for the two cyano compounds in both chloroform and polysulfone are presented, as are the PL spectra of Ooct-OPV5-CN in chloroform and polysulfone [69J. [Pg.300]


See other pages where Cyano compounds geometry is mentioned: [Pg.118]    [Pg.527]    [Pg.611]    [Pg.611]    [Pg.5]    [Pg.398]    [Pg.8]    [Pg.618]    [Pg.4]    [Pg.236]    [Pg.176]    [Pg.131]    [Pg.352]    [Pg.296]    [Pg.1096]    [Pg.81]    [Pg.538]    [Pg.1049]    [Pg.247]    [Pg.3092]    [Pg.223]    [Pg.547]    [Pg.391]    [Pg.54]    [Pg.4]    [Pg.161]    [Pg.1096]    [Pg.568]    [Pg.690]    [Pg.927]    [Pg.537]    [Pg.1048]    [Pg.568]    [Pg.214]    [Pg.62]    [Pg.645]    [Pg.627]    [Pg.198]    [Pg.200]    [Pg.203]    [Pg.206]    [Pg.212]    [Pg.213]    [Pg.880]    [Pg.286]    [Pg.591]    [Pg.591]    [Pg.90]   
See also in sourсe #XX -- [ Pg.117 , Pg.118 ]




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Cyano compounds

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