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Click chemistry functionalization improving the wideband optical-limiting performance of fullerene derivatives

机译:单击化学功能化可改善富勒烯衍生物的宽带光限制性能

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A novel kind of monodonor-bisacceptor (D-A-A) C60 charge-transfer complex was synthesized by the high-yielding [2+2] click chemistry reaction and the Prato reaction. Both electrochemical and UV-vis spectra studies were carried out and they proved that the side groups of the fullerene derivatives played an important role in the energy gaps, and also affected the third-order non-linear optical response. The experimental investigation on the third-order non-linear optical phenomena of the fullerene derivatives was measured using the Z-scan technique at different wavelengths (532 nm and 1064 nm). All the compounds exhibited very special non-linear optical properties when pumped by 21 ps pulses at 532 nm which suggested that there were two different types of reversible photo-isomerization. The optical-limiting performance has also been studied which proved indirectly the mechanism models of the reversible photo-isomerization.
机译:通过高产的[2 + 2]点击化学反应和普拉托反应,合成了一种新型的单给体-双受体(D-A-A)C60电荷转移复合物。进行了电化学和紫外可见光谱研究,他们证明了富勒烯衍生物的侧基在能隙中起着重要作用,并且还影响了三阶非线性光学响应。使用Z扫描技术在不同波长(532 nm和1064 nm)下测量了富勒烯衍生物的三阶非线性光学现象的实验研究。当以532 nm的21 ps脉冲泵浦时,所有化合物均表现出非常特殊的非线性光学性质,这表明存在两种不同类型的可逆光异构化。还研究了光限制性能,间接证明了可逆光异构化的机理模型。

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