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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Novel fluorescent 1,8-naphthalimide derivatives containing thiophene and pyrazole moieties: Synthesis by direct C-H arylation and evaluation of photophysical and electrochemical properties
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Novel fluorescent 1,8-naphthalimide derivatives containing thiophene and pyrazole moieties: Synthesis by direct C-H arylation and evaluation of photophysical and electrochemical properties

机译:含噻吩和吡唑基团的新型荧光1,8-萘二甲酰亚胺衍生物:直接C-H芳基化合成以及光物理和电化学性质的评估

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摘要

A series of novel 1,8-naphthalimide derivatives containing thiophene and pyrazole moities were synthesized by direct Pd-catalyzed C-H arylation and then characterized by 1H NMR,13C NMR,MALDI-HRMS,and elementary analysis.The photophysical and electrochemical properties of the derivatives were also investigated.All compounds have green emission both in diluted CH2Cl2 solution and solid film.The cyclic voltammetry (CV) measurements showed that the target compounds had a lowest unoccupied molecular orbital (LUMO) range from-3.49 eV to-3.29 eV and a highest occupied molecular orbital (HOMO) range from-6.04 eV to-5.81 eV.Quantum chemical calculations were performed to obtain the optimized ground-state geometry as well as the spatial distributions of the HOMO,LUMO levels of the compounds.
机译:通过直接Pd催化的CH芳基化反应合成了一系列含有噻吩和吡唑基团的新型1,8-萘二甲酰亚胺衍生物,然后通过1 H NMR,13 C NMR,MALDI-HRMS以及元素分析对其进行了表征。这些衍生物的光物理和电化学性质稀释的CH2Cl2溶液和固体膜中所有化合物均发射绿色光。循环伏安法(CV)测量表明目标化合物的未占据分子轨道(LUMO)最低,范围为3.49 eV至3.29 eV,最高分子轨道(HOMO)范围为-6.04 eV至-5.81 eV。进行了量子化学计算,以获得了优化的基态几何形状以及化合物的HOMO,LUMO含量的空间分布。

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