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Circular dichroism self-assembled molecules, chirality

The systems discussed up to now all showed chiral susceptibilities that were of the same order of magnitude or smaller than the achiral susceptibility components. The system that we discuss in this section has chiral susceptibilities that dominate the nonlinear optical response.53 The material is a chiral helicenebisquinone derivative shown in Figure 9.22. In bulk samples, the nonracemic, but not the racemic, form of the material spontaneously organizes into long fibers clearly visible under an optical microscope. These fibers comprise columnar stacks of helicene molecules.54,55 Similar columnar stacks self-assemble in appropriate solvents, such as n-dodecane, when the concentration exceeds 1 mM. This association can be observed by a large increase in the circular dichroism (CD) of the solutions. [Pg.559]


See other pages where Circular dichroism self-assembled molecules, chirality is mentioned: [Pg.282]    [Pg.302]    [Pg.135]    [Pg.167]    [Pg.212]    [Pg.2147]    [Pg.455]    [Pg.10]    [Pg.122]   


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Chiral molecules

Chiral molecules chirality

Chiral self-assembly

Circular dichroism chiral molecules

Molecules assemblies

Molecules self-assembly

Self-assembled molecules

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