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| 联吡啶钌配合物[Ru(Htcterpy)X3]3-[X=NCS,CN,Cl]的电子结构和光谱性质的理论研究 | |
| 引用本文： | 李明霞,周欣,潘清江,张红星,付宏刚,孙家锺. 联吡啶钌配合物[Ru(Htcterpy)X3]3-[X=NCS,CN,Cl]的电子结构和光谱性质的理论研究[J]. 高等学校化学学报, 2007, 28(12): 2377-2380 |
| 作者姓名： | 李明霞 周欣 潘清江 张红星 付宏刚 孙家锺 |
| 作者单位： | 1. 吉林大学理论化学研究所,理论化学计算国家重点实验室,长春,130021;黑龙江大学化学化工与材料学院,哈尔滨,150080 2. 吉林大学理论化学研究所,理论化学计算国家重点实验室,长春,130021 3. 黑龙江大学化学化工与材料学院,哈尔滨,150080 |
| 摘 要： | 利用DFT中的B3LYP方法优化了3个联吡啶钌配合物[Ru(Htcterpy)X3]3-[tcterpy=4,4',4"-tricarboxy-2,2'∶6',2"-terpyridine, X=NCS(1), CN(2), Cl(3)]的基态几何结构, 得到的几何参数与实验结果吻合得很好. 采用TD-DFT方法, 得到了配合物1~3在气态和溶液(乙醇溶液和水溶液)中的激发态电子结构和电子吸收光谱. 利用SCRF方法中的CPCM模型来模拟溶剂化效应. 研究结果表明, 配合物1~3在气态和溶液中的吸收跃迁性质相似, 低能吸收均被指认为MLCT和LLCT的混合跃迁, 高能吸收均被指认为三联吡啶配体内的π→π*跃迁. 溶剂化效应使配合物1~3在溶液中的吸收光谱蓝移. |
| 关 键 词： | 联吡啶钌配合物 电荷转移 吸收光谱 密度泛函理论 含时密度泛函理论 |
| 文章编号： | 0251-0790（2007）12-2377-04 |
| 收稿时间： | 2006-12-12 |
| 修稿时间： | 2006-12-12 |
Theoretical Studies on Electronic Structures and Spectroscopic Properties of [ Ru (Htcterpy) X3 ] 3 - [ X = NCS, CN, CI] |
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| LI Ming-Xia,ZHOU Xin,PAN Qing-Jiang,ZHANG Hong-Xing,FU Hong-Gang,SUN Chia-Chung. Theoretical Studies on Electronic Structures and Spectroscopic Properties of [ Ru (Htcterpy) X3 ] 3 - [ X = NCS, CN, CI][J]. Chemical Research In Chinese Universities, 2007, 28(12): 2377-2380 | |
| Authors: | LI Ming-Xia ZHOU Xin PAN Qing-Jiang ZHANG Hong-Xing FU Hong-Gang SUN Chia-Chung |
| Affiliation: | State Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun 130021, China;;School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080, China |
| Abstract: | The ground-structures of [Ru(Htcterpy)X3]3-[X=NCS(1), CN(2), Cl(3), tcterpy=4,4',4"-tricarboxy-2,2:6',2"-terpyridine,] are optimized by DFT method(B3LYP). The calculated geometry parameters are in agreement with the experimental values. Absorption spectra in gas phase and in solutions(ethanol and water) are predicted at the TD-DFT/B3LYP level. The solvent effects are seriously considered by using the conductor-like polarizable continuum model(CPCM). For complexes 1—3, in gas phase and solution, the low-energy absorptions have a mixed MLCT/LLCT character, whereas the high-energy absorption are attributed to the intra-ligand π→π* charge transfer transitions. Our calculations reveal the blue-shift of the absorption spectra in solution with respect to those in gas phase, agreeing with experimental observations. |
| Keywords: | Ruthenium complex Charge transfer Absorption spectra DFT TD-DFT |
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