Big Chemical Encyclopedia

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

Articles Figures Tables About

Morphology conjugated chains

Rotations around torsional barriers induce changes in chain conformation. For conjugated systems like polydiacetylenes, flow-induced changes in chain conformation can have a profound influence on the photon absorption and electronic conductivity properties of the material [73]. Flow-induced changes in molecular conformation form the basis for several technically important processes, the best known examples are the production of oriented fibers by gel spinning [74], the compatibility enhancement [75] and the shear-induced modification of polymer morphology [76]. [Pg.103]

Schwartz BJ (2003) Conjugated polymers as molecular materials how chain conformation and film morphology influence energy transfer and interchain interactions. Annu Rev Phys Chem 54 141-172... [Pg.384]

Although the above mobilities in isolated chains of conjugated polymers and in solid phases are much larger than values inferred from ToF experiments, in no case do they come close to the value of 1,000 cm /V s expected for a perfect onedimensional 7i-bonded polymer chain. Moreover, they are morphology-sensitive. [Pg.44]

Nguyen TQ, Martini IB, Liu J, Schwartz BJ (2000) Controlling interchain interactions in conjugated polymers the effects of chain morphology on exciton-exciton annihilation and aggregation in MEH-PPV films. J Phys Chem B 104 237... [Pg.206]

Pu reported the synthesis of axially chiral-conjugated polymer 82 bearing a chiral binaphthyl moiety in the main chain by the cross-coupling polymerization of chiral bifunctional boronic acid 80 with dibromide 81 (Equation (39)). The polymer is soluble in common organic solvents, such as THE, benzene, toluene, pyridine, chlorobenzene, dichloromethane, chloroform, and 1,2-dichloroethane. The polymer composed of racemic 80 was also synthesized, and the difference of characteristics was examined. Optically active polymer 82 was shown to enhance fluorescence quantum yield up to = 0.8 compared with the racemic 82 ( = 0.5). Morphologies of the optically active and racemic polymers were also compared with a systematic atomic-force microscopy (AEM). [Pg.666]


See other pages where Morphology conjugated chains is mentioned: [Pg.56]    [Pg.402]    [Pg.171]    [Pg.544]    [Pg.564]    [Pg.250]    [Pg.311]    [Pg.341]    [Pg.87]    [Pg.149]    [Pg.97]    [Pg.22]    [Pg.50]    [Pg.203]    [Pg.207]    [Pg.855]    [Pg.856]    [Pg.241]    [Pg.36]    [Pg.307]    [Pg.7]    [Pg.47]    [Pg.57]    [Pg.285]    [Pg.335]    [Pg.311]    [Pg.363]    [Pg.201]    [Pg.241]    [Pg.36]    [Pg.53]    [Pg.53]    [Pg.1551]    [Pg.1587]    [Pg.159]    [Pg.192]    [Pg.171]    [Pg.154]    [Pg.216]    [Pg.206]    [Pg.115]    [Pg.191]    [Pg.197]    [Pg.340]    [Pg.650]   
See also in sourсe #XX -- [ Pg.87 ]




SEARCH



Chain conjugation

Conjugated chain

Conjugated morphology

© 2024 chempedia.info