We have studied the structural and optical properties of four 2,5-diphenyl-1,4-distyrylbenzene derivatives with all cis double bonds. These compounds belong to a class of nonplanar conjugated compounds possessing a typical Aggregation-Induced Emission (AIE) property that has no emission in solution but intense emission in crystal. The four molecules are packed in different stacking modes with different intermolecular interactions, resulting in different crystalline state photoluminescence (PL) efficiency. The torsional molecular configuration increases the intermolecular distances effectively in the crystalline state, which decreases the difference of the optical properties from the frozen isolated molecules to the crystalline state. The Stokes shifts of these compounds are very large and the PL spectra have only one broad emission band with poor structure, due to the relatively large configuration difference between the ground state and the first singlet excited state, and the abundant vibration energy levels of the torsional molecule with changeable conformation.
The mechanism of DNA assembly is revealed by analyzing the energy barriers during nucleation and growth. The assembly is controlled by two competing parameters: the conformation adjustment rate of DNA strands and the spreading rate of new strands on the nuclei surface, both of which are temperature dependent and can be tuned by sequence design.
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