Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Dendrimer photoisomerisation

The stilbene carbon unit has also been peripherally bound to POPAM cores. Although it does not strictly belong to the hydrocarbon dendrimers, the formula of a G2 dendrimer of this type (Fig. 4.21) is depicted here as an example. It was obtained by alkylation of the corresponding eightfold mono-sulphonamide with 4-(bromomethyl)stilbene. Its fluorescence, E/Z isomerisation, photoisomerisation (see Section 5.2.2), and excimer formation were compared with those of non-dendritic stilbenes. The quantum yields of photoisomerisation (0.30) and fluorescence of the E isomer (0.014) of the dendrimer proved to be substantially lower [38]. [Pg.101]

A light-controlled dendritic box was investigated in analogous fourth-generation POPAM dendrimers whose periphery alternately bore azobenzene and naphthyl moieties. Measurements of photoisomerisation at a wavelength of 365 nm in dichloromethane showed that not all azobenzene units in the E form are transformed into the Z form, but that, for example, four units remain in the E form and some 28 units isomerise to the Z form. At pH 7, six eosin molecules per host molecule were taken up by this mixture of isomers. On the other hand, the dendrimer having all azobenzene groups in the E form takes... [Pg.211]


See other pages where Dendrimer photoisomerisation is mentioned: [Pg.176]    [Pg.177]    [Pg.179]    [Pg.181]    [Pg.183]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.191]    [Pg.191]    [Pg.211]    [Pg.238]   
See also in sourсe #XX -- [ Pg.176 ]




SEARCH



Antenna effect and photoisomerisation of dendrimers

Photoisomerisation

© 2024 chempedia.info