Abstract
Oligosilanyl-bridged systems are expected to give rise to unique optoelectronic properties because of σ-πconjugation between the Si-Si σ orbital and the aryl πorbital. Herein, we synthesized a small series of novel biscarbazoles bridged with permethylated oligosilanyl units (-[Si(CH3)2]n-, n = 1-4) and examined their spectroscopic properties in detail. In the target molecules BCzSin, n = 2-4, the efficient σ-πconjugation elevated the highest occupied molecular orbital energy level with no influence on the lowest unoccupied molecular orbital. In the solid state, the emission full width at half-maximum (fwhm) of all the compounds narrowed significantly, while the emission efficiency increased and the emission color of carbazole was retained. This research provided a very simple and general way of subtly manipulating the electronic properties of organic materials to construct an emissive color-retaining system for multifunctional applications.
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CITATION STYLE
Feng, S., Zhou, Z., Xiang, X., Feng, H., Qu, Z., & Lu, H. (2020). Oligosilanyl-Bridged Biscarbazoles: Structure, Synthesis, and Spectroscopic Properties. ACS Omega, 5(30), 19181–19186. https://doi.org/10.1021/acsomega.0c02559
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