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Spirooxazine-based multifunctional molecular switches with tunable photochromism and nonlinear optical response

机译:具有可调光致变色和非线性光学响应的​​基于螺恶嗪的多功能分子开关

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摘要

A new type of organic photochromic spirooxazine has been synthesized, incorporating increasing numbers of thiophene units by vinyl bridges. These compounds exhibit tunable photochromic properties that are sensitive to low-energy visible light compared with traditional UV. Furthermore, the ring-opening mechanism is put in relation to the interaction of fragment molecular orbitals. The result shows that the effective excitation with significant intensity is centred mainly on the naphthoxazine part and vinyl thiophene plays a crucial role in the photochemical and photophysical process. Density functional calculations are performed to rationalize the "on and off" switching nonlinear optical behaviors of compounds, showing the potential for applying the materials in nonlinear optical switches.
机译:已经合成了一种新型的有机光致变色螺恶嗪,其通过乙烯基桥结合了越来越多的噻吩单元。与传统的UV相比,这些化合物具有可调谐的光致变色特性,对低能可见光敏感。此外,开环机理与片段分子轨道的相互作用有关。结果表明,高强度的有效激发主要集中在萘并恶嗪部分上,乙烯基噻吩在光化学和光物理过程中起着至关重要的作用。进行密度泛函计算以合理化化合物的“开和关”切换非线性光学行为,显示出将材料应用于非线性光学开关的潜力。

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