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

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.

[1]  Saqib Ali,et al.  SYNTHESIS AND SPECTRAL STUDIES OF DI- AND TRIORGANOTIN(IV) COMPLEXES WITH 2-(6-METHOXYNAPHTHYL)PROPIONIC ACID (NAPROXEN) , 2002 .

[2]  M. Holčapek,et al.  Structure and in vitro antifungal activity of [2,6‐bis(dimethylaminomethyl)phenyl]diphenyltin(IV) compounds , 2002 .

[3]  M. Nath,et al.  Organotin(IV) complexes of amino acids and peptides , 2001 .

[4]  Saqib Ali,et al.  Synthesis, Spectroscopic Characterization and Biological Studies of Organotin Derivatives of 2- (2,6-dichlorophenyl)aminophenylaceticacid , 2000 .

[5]  M. Lautens,et al.  Metal-catalyzed hydrostannations. , 2000, Chemical reviews.

[6]  M. Sarwar,et al.  Thermal Degradation of Poly (vinyl chloride)-Stabilization Effect of Dichlorotin Dioxine , 2000 .

[7]  E. Tiekink,et al.  Correlating Mossbauer and solution- and solid-state Sn-117 NMR data with X-ray diffraction structural data of triorganotin 2-[(E)-2-(2-hydroxy-5-methylphenyl)-1-diazenyl]benzoates , 1998 .

[8]  Saqib Ali,et al.  1H, 13C, 119Sn NMR, 119mSn Mössbauer, Infrared and Mass Spectrometric Studies of Organotin Carboxylates of 2-(2,3-dimethylphenyl)Aminobenzoic Acid and their Effect on Microorganisms. , 1997 .

[9]  E. Tiekink,et al.  Synthesis, characterization and in vitro antitumour activity of triphenyl- and tri-n-butyltin benzoates, phenylacetates and cinnamates , 1997 .

[10]  Saqib Ali,et al.  Mössbauer, multinuclear magnetic resonance and mass spectrometric studies of organotin carboxylates of m-methyltrans-cinnamic acid , 1995 .

[11]  Saqib Ali,et al.  Organotin esters of 3-(2-furanyl)-2-propenoic acid: their characterization and biological activity , 1995 .

[12]  E. Tiekink,et al.  Structural chemistry of organotin carboxylates. XVII: Diorganotin(IV) derivatives of N-phthaloyl-DL-valine , 1992 .

[13]  G. K. Sandhu,et al.  Diorganotin(IV) Derivatives of Thiophene-2-carboxylic Acid , 1990 .

[14]  P. G. Harrison Chemistry of tin , 1989 .

[15]  E. Tiekink,et al.  Structural chemistry of organotin carboxylates , 1989 .

[16]  E. M. Holt,et al.  Solution and solid-state molecular structures of Me2Sn(OAc)2 and its hydrolyzate, ([Me2Sn(OAc)]2O)2, by solution and solid-state carbon-13 NMR. X-ray diffraction study of the hydrolyzate , 1986 .

[17]  T. Al-Allaf Carbon-13 NMR studies of some organotin(IV) compounds , 1986 .

[18]  D. E. Nichols,et al.  Brine shrimp: a convenient general bioassay for active plant constituents. , 1982, Planta medica.

[19]  J. Otera,et al.  119Sn Chemical Shifts in five- and six-coordinate organotin chelates , 1981 .

[20]  Glen B. Deacon,et al.  Relationships between the carbon-oxygen stretching frequencies of carboxylato complexes and the type of carboxylate coordination , 1980 .

[21]  Y. Kondo,et al.  Antimalarial phenanthrene amino alcohols.1. Fluorine-containing 3- and 6-substituted 9-phenanthrenemethanols. , 1971, Journal of medicinal chemistry.

[22]  W. R. Adams,et al.  Photochemical transformations. XXII. Photoisomerization of substituted acrylic acids and acrylamides to .beta.-lactones and .beta.-lactams , 1968 .

[23]  Saqib Ali,et al.  Synthesis, characterization, and biological studies of tri‐ and diorganotin(IV) complexes with 2′,4′‐difluoro‐4‐hydroxy‐[1,1′]‐biphenyle‐3‐carbolic acid: Crystal structure of [(CH3)3Sn(C13H7O3F2)] , 2002 .

[24]  Atta-ur-Rahman,et al.  Bioassay Techniques for Drug Development , 2001 .

[25]  B. Mahieu,,et al.  ORGANOTIN(IV) DERIVATIVES OF 3,4-(METHYLENEDIOXY) PHENYLACETIC ACID: SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND IN VITRO ANTITUMOUR PROPERTIES , 2000 .

[26]  Saqib Ali,et al.  SYNTHESIS AND SPECTRAL STUDIES OF BIS{DIALKYL- [TRANS-3-(2-THIOPHENYL)-2-PROPENOATO]TIN} OXIDES: CRYSTAL STRUCTURE OF {[(CH3)2SnO2C-CH=CH-C4H3S]2O}2 , 1996 .

[27]  L. Jiang,et al.  PREPARATION, STRUCTURE AND BIOLOGICAL ACTIVITIES OF MIXED METHYLDICYCLOHEXYLTIN CARBOXYLATES , 1996 .

[28]  H. Schönenberger “Metal Complexes in Cancer Chemotherapy”, Edited by Bernhard K. Keppler, VCH Verlagsgesellschaft – Weinheim, New York, Basel, Cambridge, Tokyo, 1993, 436 S., DM 196, ‐ , 1994 .

[29]  B. Keppler Metal complexes in cancer chemotherapy , 1993 .

[30]  S. Shaukat,et al.  Herbicide influence on germination and seedling growth of Vigna mungo (L) Hepper and V. radiata (L) Wilczek. , 1980 .

[31]  D. D. Perrin,et al.  Purification of Laboratory Chemicals , 2022 .