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3,5-Dianilino Substituted Difluoroboron Dipyrromethene: Synthesis, Spectroscopy, Photophysics, Crystal Structure, Electrochemistry, and Quantum-Chemical Calculations

机译:3,5-二苯胺基取代的二氟硼双吡咯烷:合成,光谱学,光物理,晶体结构,电化学和量子化学计算

摘要

4,4-Difluoro-3,5-bis(phenylamino)-8-(4-tolyl)-4-bora-3a,4a-diaza-s-indacene (1), a symmetric fluorescent difluoroboron dipyrromethene dye, has been synthesized by nucleophilic substitution of 3,5-dichloro-4,4-ifluoro-8-(4-tolyl)-4-bora-3a,4a-diaza-s-indacene with aniline. The solvent-dependent spectroscopic and photophysical properties have been investigated by means of UV-vis spectrophotometry and steady-state and time-resolved fluorometry and are compared to those of the nonsymmetrically substituted 5-chloro-4,4-ifluoro-3-phenylamino-8-(4-tolyl)-4-bora-3a,4a-diaza-s-indacene (2). A new, generalized treatment of the solvent effect, proposed by Catalan (J. Phys. Chem. B 2009, 113, 5951-5960) and based on a set of four mutually independent, empirical scales (dipolarity, polarizability, acidity, and basicity of the medium) is the most appropriate for describing the solvatochromic shifts of the UV-vis absorption and fluorescence emission of 1 and 2. In contrast to the nonsymmetric compound 2, the symmetric dye 1 has higher fluorescence quantum yields (0.45-0.86) and longer fluorescence lifetimes (3.36-4.03 ns) in all solvents studied and its emission maxima are shifted bathochromically by similar to 45 rim. Large differences are also evident in the redox electrochemistry of the two dyes, with the symmetric analogue 1 possessing a much lower oxidation potential (similar to 600 mV) than the nonsymmetric 2. The absorption bandwidths and Stokes shifts of symmetric 1 are much smaller than those for nonsymmetric 2. For both dyes, the value of the fluorescence rate constant, [k(f) = (1.7 +/- 0.3) x 10(8) s(-1)], does not depend much on the solvent tested. X-ray diffraction analysis of 1 shows that the BODIPY core possesses a planar structure. Quantum-chemical calculations support the different photophysical behavior of the symmetric derivative 1 vis-a-vis the nonsymmetric 2.
机译:4,4-二氟-3,5-双(苯氨基)-8-(4-甲苯基-4--4-硼-3a,4a-二氮杂-s-茚并四烯(1),已经合成了对称的荧光二氟硼二吡咯亚甲基染料通过用苯胺亲核取代3,5-二氯-4,4-ifluoro-8-(4-甲苯基)-4-bora-3a,4a-diaza-s-indacene。已通过紫外可见分光光度法,稳态和时间分辨荧光法研究了溶剂依赖性光谱和光物理性质,并将其与非对称取代的5-氯-4,4-i氟-3-苯基氨基- 8-(4-甲苯基)-4-硼-3a,4a-二氮杂-s-茚并二烯(2)。加泰罗尼亚语(J. Phys。Chem。B 2009,113,5951-5960)提出了一种新的,通用的溶剂效应处理方法,该方法基于一组四个相互独立的经验尺度(偶极性,极化性,酸度和碱度)最适合于描述1和2的紫外可见吸收和荧光发射的溶剂化变迁。与非对称化合物2相比,对称染料1的荧光量子产率更高(0.45-0.86),而在所有研究的溶剂中都有更长的荧光寿命(3.36-4.03 ns),并且其发射最大值在红移方向上发生了约45个边缘的红移。两种染料的氧化还原电化学反应也存在明显差异,对称类似物1的氧化电位(类似于600 mV)比非对称染料2的氧化电位低得多。对称染料1的吸收带宽和斯托克斯位移远小于对称染料1的吸收带宽和斯托克斯位移。对于非对称2。对于两种染料,荧光速率常数[k(f)=(1.7 +/- 0.3)x 10(8)s(-1)]的值在很大程度上与测试的溶剂无关。 1的X射线衍射分析表明,BODIPY芯具有平面结构。量子化学计算支持对称衍生物1与非对称化合物2的不同光物理行为。

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