Synthesis, Spectroscopic Characterization: (IR, Multinuclear NMR, 119mSn Mössbauer and Mass Spectrometry), and Biological Activity (Antibacterial, Antifungal, and Cytotoxicity) of Di‐ and Triorganotin(IV) Complexes of (E)‐3‐(4‐Chlorophenyl)‐2‐phenylpropenoic Acid

Sadiq-ur-Rehman, Saqib Ali, A. Badshah, M. Mazhar, Xueqing Song, G. Eng, K. Khan
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引用次数: 10

Abstract

Abstract In an effort to develop new organotin(IV) compounds of industrial and biological importance, a series of di‐ and triorganotin(IV) complexes of (E)‐3‐(4‐chlorophenyl)‐2‐phenylpropenoic acid with the general formula R4‐n SnL n have been synthesized by the reaction of the corresponding organotin chlorides with the sodium salt of (E)‐3‐(4‐chlorophenyl)‐2‐phenylpropenoic acid (C15H10ClO2Na) where, R = CH3, C2H5, n‐C4H9, C6H5, C6H5 · CH2, n = 1 or 2 and L = acid anion (C15H10ClO2 −). The dimeric tetraorganodicarboxylatodistannoxanes [(Me2SnL)2O]2 compound (2) and [(Bu2SnL)2O]2 compound (4), L = C15H10ClO2 −, were synthesized by the reaction of R2SnO with the ligand acid (HL) in 1:1 molar ratio with azeotropic removal of water. The structures of the complexes are discussed on the basis of IR, multinuclear (1H, 13C, 119Sn) NMR, 119mSn Mössbauer spectroscopies and mass spectrometry. The spectroscopic results substantiate that all the diorganotin(IV) derivatives possess trigonal‐bipyramidal structures in solution and octahedral geometry in the solid state. A linear polymeric trigonal‐bipyramidal structure in the solid state and a tetrahedral environment around the tin atom in non‐coordinating solvents has been proposed for the triorganotin(IV) derivatives. The Δν [Δν = νasym(COO) − νsym(COO)] values obtained from the IR data, in comparison to the ligand acid and its sodium salt, fall in the range which shows that the ligand may act as a bidentate coordinating group through the carboxyl (COO) oxygen atoms. The biological activity and LD50 data of the synthesized compounds are also reported. The triorganotin(IV) complexes exhibit significantly better activities than the diorganotin(IV) derivatives. The LD50 data show that most of the investigated compounds are cytotoxic.
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合成,光谱表征:(IR,多核磁共振,119mSn Mössbauer和质谱),以及(E)‐3‐(4‐氯苯基)‐2‐苯基丙烯酸二和三有机锡(IV)配合物的生物活性(抗菌,抗真菌和细胞毒性)
抽象,以开发新的有机锡化合物(IV)的工业和生物的重要性,一系列的di》triorganotin (IV)复合物(E)检测3量高chlorophenyl区域(4)量2 phenylpropenoic酸与一般公式R4检测n SnL被相应的反应合成有机锡氯化物的钠盐(E)量3量高chlorophenyl区域(4)量2列车phenylpropenoic酸(C15H10ClO2Na), R = CH3 C2H5, n高C4H9 C6H5, C6H5·CH2, n = 1或2和L =酸阴离子(C15H10ClO2−)。用R2SnO与配体酸(HL)以1:1的摩尔比反应共沸脱水,合成了四有机二羧酸二聚体[(Me2SnL)2O]2化合物(2)和[(Bu2SnL)2O]2化合物(4),L = C15H10ClO2−。利用红外光谱、多核(1H, 13C, 119Sn) NMR、119mSn Mössbauer光谱和质谱分析对配合物的结构进行了分析。光谱结果证实所有的二有机锡(IV)衍生物在溶液中具有三角双锥体结构,在固体中具有八面体结构。本文提出了三有机锡(IV)衍生物在固体状态下的线性聚合物三角双锥体结构和在非配位溶剂中锡原子周围的四面体环境。红外数据得到的Δν [Δν = νsym(COO)−νsym(COO)]值与配体酸及其钠盐相比,落在该范围内,表明配体可能通过羧基(COO)氧原子作为双齿配位基。并报道了所合成化合物的生物活性和LD50数据。三有机锡(IV)配合物的活性明显优于二有机锡(IV)衍生物。LD50数据表明,大多数所研究的化合物具有细胞毒性。
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