Two new dendronized nonlinear optical (NLO) polyfluorenes were synthesized with high azochromophore loading density by the introduction of high generation chromophore dendrons on the side chains. Thanks to the advantages of Sharpless' click chemistry reaction, the dendrons were conveniently bonded to the backbone of polyfluorene with the conversion of 100%, although they were really very bulky. The new-formed triazole rings in the dendrons acted as suitable isolation groups to minimize the strong dipole-dipole interactions among the polar chromophore moieties to improveNLO effects, according to the results obtained from UV-vis spectra and order parameters. All the polymers were well characterized and exhibited good solubility, high thermal ability, wide optical window, and largeNLOeffects (up to 106.0 pm/V). In addition, the testedNLOresults of these dendronzied polymers demonstrated a deviation from the dipolar frustration that typically limits the NLO effect in conventional chromophore/polymer composite materials, indicating that the frequently observed asymptotic dependence of electro-optic activity on chromophore density may be overcome through rational design.

A novel series of indole-based conjugated oligomers were synthesized by Wittig-Horner-Emmons olefination from the aryl-bridged bisindole aldehydes and the corresponding bisphosphonates. The introduction of indole into the light-emitting materials made these oligmers exhibit favorable properties. They were thermally stable, and the UV-vis spectra of the oligomers could be modulated by the arylenevinylene units; their PL and EL spectra also showed similar properties that can be further modulated. The highest luminance achieved in a device with the configuration ITO/PEDOT:PSS/oligomer/Ba/Al was 2536 cd/m2 at 7.5 V for oligomer P6, and the highest external EL quantum efficiency of 0.39% and luminous efficiency of 0.97 cd/A were attained by oligomer P1.

Two indole-based organic dyes were conveniently prepared and well characterized. The triphenylamine or carbazole moieties were bonded to the indole group acting as a potential electron donor, which can tune the HOMO and LUMO levels of the resultant dye, and another triphenylamine or carbazole group was linked to the pyrrole ring on the nitrogen atom, which was expected to suppress the aggregation of the dye in the solid state to some degree. These two dyes were utilized as dye sensitizers in dye-sensitized solar cells and demonstrated efficient photon-to-electron conversion properties.

In this paper, two new series of main-chain and side-chain second-order nonlinear optical (NLO) polyurethanes have been successfully prepared, in which isolation groups with different sizes were introduced to adjust the NLO property of the resultant polymers, according to the concept of "suitable isolation groups". The second harmonic generation (SHG) experiments demonstrated that all the polymers exhibited large second harmonic generation (SHG) coefficients of d33 values (up to 105.6 pm/V) with excellent thermal stability and filmforming ability, indicating that the introduction of isolation groups could alleviate the "nonlinearity-stability trade off" efficiently. In addition, for both main-chain and side-chain polymers, BOP acted as the suitable isolation group. It was also found that the positive influence of the linked suitable isolation spacer was more obvious in the main-chain polymers, in comparison with those in the side-chain polymers.

A series of new carbazole-based luminophores (1-12) were synthesized and well characterized, which demonstrated aggregation-induced emission enhancement (AIEE) properties. The obtained experimental results demonstrated that the attachment of aromatic rotors to luminophore moieties would lead to the decreased quantum yields (measured in diluted solutions); the more rotors attached, the smaller the quantum yields tested. This further confirmed that the AIEE phenomena were caused by the restriction of the intramolecular vibrational and rotational motions in an indirect manner.