Ngoy Bokolombe P, May Aviwe K, Mack John, Nyokong Tebello
Department of Chemistry, Institute for Nanotechnology Innovation, Rhodes University, Makhanda, South Africa.
Département de Chimie, Université de Kinshasa, Kinshasa, Democratic Republic of the Congo.
Front Chem. 2019 Oct 31;7:740. doi: 10.3389/fchem.2019.00740. eCollection 2019.
The optical limiting (OL) properties of a 3,5-di--benzyloxystyrylBODIPY dye with an -acetamidophenyl moiety at the -position have been investigated by using the open-aperture Z-scan technique at 532 nm with 10 ns laser pulses. There is a ca. 140 nm red shift of the main spectral band to 644 nm relative to the corresponding BODIPY core dye, due to the incorporation of -benzyloxystyryl groups at the 3,5-positions. As a result, there is relatively weak absorbance across most of the visible region under ambient light conditions. Analysis of the observed reverse saturable absorbance (RSA) profiles demonstrates that the dye is potentially suitable for use in optical limiting applications as has been reported previously for other 3,5-distyrylBODIPY dyes. Time-resolved transient absorption spectroscopy and kinetic studies with femtosecond and nanosecond scale laser pulses provide the first direct spectral evidence that excited state absorption (ESA) from the S state is responsible for the observed OL properties.
通过使用开孔Z扫描技术,在532nm波长下用10ns激光脉冲研究了一种在β位带有α-乙酰氨基苯基部分的3,5-二-β-苄氧基苯乙烯基BODIPY染料的光学限幅(OL)特性。相对于相应的BODIPY核心染料,由于在3,5位引入了β-苄氧基苯乙烯基,主光谱带出现了约140nm的红移,至644nm。因此,在环境光条件下,该染料在大部分可见光区域的吸光度相对较弱。对观察到的反向饱和吸收(RSA)曲线的分析表明,该染料可能适用于光学限幅应用,正如之前报道的其他3,5-二苯乙烯基BODIPY染料一样。飞秒和纳秒级激光脉冲的时间分辨瞬态吸收光谱和动力学研究提供了首个直接光谱证据,表明来自S态的激发态吸收(ESA)是观察到的OL特性的原因。