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Synthesis, crystal structure, spectroscopic characterization and nonlinear optical properties of manganese (II) complex of picolinate: A combined experimental and computational study

机译:吡啶甲酸锰(II)配合物的合成,晶体结构,光谱表征和非线性光学性质:实验和计算研究相结合

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A novel manganese (II) complex with picolinic acid (pyridine 2-carboxylic acid, Hpic), namely, [Mn(pi-c)(2)(H2O)(2)] was prepared and its crystal structure was fully characterized by using single crystal X-ray diffraction. Picolinate (plc) ligands were coordinated to the central manganese(II) ion as bidentate N,O-donors through the nitrogen atoms of pyridine rings and the oxygen atoms of carboxylate groups forming five-membered chelate rings. The spectroscopic characterization of Mn(II) complex was performed by the applications of FT-IR, Raman, UV-vis and EPR techniques. In order to support these studies, density functional theory (DFT) calculations were carried out by using B3LYP level. IR and Raman spectra were simulated at B3LYP level, and obtained results indicated that DFT calculations generally give compatible results to the experimental ones. The electronic structure of the Mn(II) complex was predicted using time dependent DFT (TD-DFT) method with polarizable continuum model (PCM). Molecular stability, hyperconjugative interactions, intramolecular charge transfer (ICT) and bond strength were investigated by applying natural bond orbital (NBO) analysis. Nonlinear optical properties of Mn(II) complex were investigated by the determining of molecular polarizability (alpha) and hyperpolarizability (beta) parameters. (C) 2015 Elsevier B.V. All rights reserved.
机译:制备了一种新的与吡啶甲酸的锰(II)配合物(吡啶2-羧酸,Hpic),即[Mn(pi-c)(2)(H2O)(2)],并通过使用单晶X射线衍射。吡啶甲酸(plc)配体通过吡啶环的氮原子和形成五元螯合环的羧基的氧原子配位为中心锰(II)离子作为二齿N,O供体。 Mn(II)配合物的光谱表征是通过FT-IR,拉曼,UV-vis和EPR技术进行的。为了支持这些研究,使用B3LYP水平进行了密度泛函理论(DFT)计算。在B3LYP水平上模拟了IR和拉曼光谱,获得的结果表明DFT计算通常与实验结果具有可比性。 Mn(II)配合物的电子结构是使用具有极化连续体模型(PCM)的时间依赖性DFT(TD-DFT)方法预测的。通过应用自然键轨道(NBO)分析研究了分子稳定性,超共轭相互作用,分子内电荷转移(ICT)和键强度。通过确定分子极化率(alpha)和超极化率(beta)参数,研究了Mn(II)配合物的非线性光学性质。 (C)2015 Elsevier B.V.保留所有权利。

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