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首页> 外文期刊>Asian journal of research in chemistry >Spectrophotometric and Spectroscopic studies of charge transfer complexes of Benzamide as an electron donor with Picric acid as an electron acceptor in different polar solvents
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Spectrophotometric and Spectroscopic studies of charge transfer complexes of Benzamide as an electron donor with Picric acid as an electron acceptor in different polar solvents

机译:分光光度法和分光镜研究不同极性溶剂中苯甲酰胺作为电子给体与苦味酸作为电子受体的电荷转移配合物

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The charge transfer complexes of the donor benzamide (BZ),with K-acceptor picric acid (PA) have been studied spectrophotometrically in various solvents such as carbon Jetra chloride, ethanol, and methanol at room temperature using absorption spectrophotometer. The results indicate that formation of CTC in less polar solvent is high. The stoichiometry of the CT complex was found to be 1:1. The physical parameters of CT complex were evaluated by the Benesi-Hildebrand equation. The data are discussed in terms of formation constant (K_(CT)), molar extinction coefficient (εCT), standard free energy (ΔG~0 ), oscillator strength(f), transition dipole moment (nEN), resonance energy (R_N) and ionization potential (I_D). The results indicate that the formation constant (K_(CT() for the complex were shown to be dependent upon the nature of electron acceptor, donor and polarity of solvents which were used. The results show that a charge transfer molecular complex between picric acid and benzamide stabilized by hydrogen bonding. The formation of the complex has been confirmed by UV-visible, FT-IR, ~1H-NMR, TGA/DTA spectral data methods. On the basis of the studies, the structure of CT complex is [(BZ) (PA) , and a general mechanism for its formation is proposed.
机译:在室温下,使用吸收分光光度计,在各种溶剂(如Jetra氯化碳,乙醇和甲醇)中,使用分光光度法研究了供体苯甲酰胺(BZ)与K-受体苦味酸(PA)的电荷转移络合物。结果表明,在极性较小的溶剂中四氯化碳的形成很高。发现CT复合物的化学计量为1:1。通过Benesi-Hildebrand方程评估CT复合体的物理参数。根据形成常数(K_(CT)),摩尔消光系数(εCT),标准自由能(ΔG〜0),振荡器强度(f),跃迁偶极矩(nEN),共振能(R_N)讨论数据和电离势(I_D)。结果表明,配合物的形成常数(K_(CT())取决于电子受体的性质,给体和所用溶剂的极性。结果表明,苦味酸和通过氢键稳定的苯甲酰胺,通过紫外可见光,FT-IR,〜1H-NMR,TGA / DTA光谱数据方法证实了配合物的形成。在研究的基础上,CT配合物的结构为[[( BZ)(PA),并提出了其形成的一般机制。

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