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Deep-Red Emissive BODIPY-Chlorin Arrays Excitable with Green and Red Wavelengths

机译:激发波长为绿色和红色的深红色发射BODIPY-Chlorin阵列

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摘要

We report here the synthesis and characterization of BODIPY-chlorin arrays containing a chlorin subunit, with tunable deep-red (641-685 nm) emission, and one or two BODIPY moieties, absorbing at 504 nm. Two types of arrays were examined: one where BODIPY moieties are attached through a phenylacetylene linker at the 13- or 3,13-positions of chlorin, and a second type where BODIPY is attached at the 10-position of chlorin through an amide linker. Each of the examined arrays exhibits an efficient (>= 0.80) energy transfer from BODIPY to the chlorin moiety in both toluene and DMF and exhibits intense fluorescence of chlorin upon excitation of BODIPY at similar to 500 nm. Therefore, the effective Stokes shift in such arrays is in the range of 140-180 nm. Dyads with BODIPY attached at the 10-position of chlorin exhibit a bright fluorescence in a range of solvents with different polarities (i.e., toluene, MeOH, DMF, and DMSO). In contrast to this, some of the arrays in which BODIPY is attached at the 3- or at both 3,13-positons of chlorin exhibit significant reduction of fluorescence in polar solvents. Overall, dyads where BODIPY is attached at the 10-position of chlorin exhibit similar to 5-fold brighter fluorescence than corresponding chlorin monomers, upon excitation at 500 nm.
机译:我们在此报告BODIPY-二氢卟酚阵列的合成和表征,该阵列包含二氢卟酚亚基,具有可调的深红色(641-685 nm)发射,以及一个或两个BODIPY部分,在504 nm处吸收。检查了两种类型的阵列:一种是通过苯乙炔连接基将BODIPY部分连接在二氢卟酚的13位或3,13位,另一种是通过酰胺连接基将BODIPY连接在二氢卟酚的10位。每个检查的阵列在甲苯和DMF中均显示出有效的(> = 0.80)从BODIPY到二氢卟酚部分的能量转移,并在BODIPY激发类似于500 nm时显示出强烈的二氢卟酚荧光。因此,在这种阵列中的有效斯托克斯位移在140-180nm的范围内。在二氢卟酚的10位上连接了BODIPY的染料在一系列极性不同的溶剂(例如甲苯,MeOH,DMF和DMSO)中显示出明亮的荧光。与此相反,在BODIPY在二氢卟酚的3-或两个3,13位上均连接的某些阵列中,极性溶剂中的荧光显着降低。总体而言,在500 nm激发时,BODIPY连接在二氢卟酚10位的二元组显示出比相应二氢卟酚单体亮5倍的荧光。

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