量子产额
光化学
发色团
激发态
荧光
斯托克斯位移
化学
平面度测试
溶剂
吸收(声学)
位阻效应
材料科学
光学
有机化学
原子物理学
结晶学
复合材料
物理
作者
Jorge Bañuelos,F. López Arbeloa,Virginia Martínez‐Martínez,Teresa Arbeloa,Íñigo López‐Arbeloa
摘要
UV−vis absorption spectroscopy and fluorescence (steady-state and time-resolved) techniques were used to study the photophysical properties of the pyrromethene 597 (PM597) dye in several solvents, which include a wide range of apolar, polar, and protic media. This dye presents a lower fluorescence quantum yield than the well-known PM567 dye because of an increase in the nonradiative deactivation rate constant. This is attributed to a loss of planarity in the excited state provided by the steric hindrance of the tert-butyl groups at positions 2 and 6 of the chromophore core. Such a geometrical change in the excited state leads to an important Stokes shift, reducing the reabsorption and reemission effects in the detected emission in highly concentrated dye solutions. The highest fluorescence quantum yield of PM597 is observed in polar media.
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