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Journal articles on the topic 'Diorganotin dichloride'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Deep, Gagan, Deepali Chaturvedi, and A. K. Narula. "Guanylurea derivatives of diorganotin(IV) dichloride." Journal of Coordination Chemistry 62, no. 12 (2009): 2058–66. http://dx.doi.org/10.1080/00958970902756044.

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2

Al-Allafb, Talal A. K., and Amer Abdul-Rahman. "Diorganotin (IV) Dichloride Complexes of some N-Arylfurfuralnitrones." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 27, no. 7 (1997): 985–96. http://dx.doi.org/10.1080/00945719708000241.

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3

Ma, Chunlin, Junhong Zhang, and Rufen Zhang. "Syntheses, characterization, and X-ray crystal structures of diorganotin(IV) derivatives of 2-pyridinethiolato-N-oxide." Canadian Journal of Chemistry 81, no. 10 (2003): 1070–75. http://dx.doi.org/10.1139/v03-134.

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The diorganotin(IV) dichloride reacts with sodium 2-pyridinethiolato-N-oxide in a 1:1 ratio to produce [Me2SnCl(2-SpyO)] (1), [Et2SnCl(2-SpyO)] (2), [Bu2SnCl(2-SpyO)] (3), [Ph2SnCl(2-SpyO)] (4), and [(PhCH2)2SnCl(2- SpyO)] (5). The new complexes have been characterized by elemental analysis and IR and NMR (1H, 119Sn, and 13C) spectroscopy. On the basis of 119Sn NMR data the effective coordination number in solution is five. The structures 1 and 4 have been confirmed by X-ray crystallography. Crystals of 1 are triclinic with space group P[Formula: see text] and those of 4 are monoclinic, P21/n.

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4

Abbas, Zahoor, Manoj Kumar, Hardeep Singh Tuli, et al. "Synthesis, Structural Investigations, and In Vitro/In Silico Bioactivities of Flavonoid Substituted Biguanide: A Novel Schiff Base and Its Diorganotin (IV) Complexes." Molecules 27, no. 24 (2022): 8874. http://dx.doi.org/10.3390/molecules27248874.

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Quercetin is one of the most powerful bioactive dietary flavonoids. The in vivo biological study of quercetin is extremely difficult due to its very low solubility. However, diorganotin complexes of quercetin are more useful when contrasted with quercetin due to increased solubility. In the present study, quercetin, substituted biguanide synthesized in the form of Schiff base and its di-alkyl/aryl tin (IV) complexes were obtained by condensing Schiff base with respective di-alkyl/aryl tin (IV) dichloride. Advanced analytical techniques were used for structural elucidation. The results of biolo

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5

PADAM, NABH NAGAR. "Addition Complexes of Dialkyl Phosphonates with Tin(IV) and Organotin(IV) Chlorides." Journal of Indian Chemical Society Vol. 67, Sep 1990 (1990): 703–5. https://doi.org/10.5281/zenodo.6204126.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 <em>Manuscript received 15 May 1989, revised 19 February 1990, accepted 11 May 1990</em> Addition complexes of dialkyl phosphonates with tin(IV) chloride, diorganotin dichloride and triorganotin chloride have been prepared and characterised on the basis of ir and nmr (<sup>1</sup>H, <sup>31</sup>P and <sup>1 1 9</sup>Sn) spectral data. Dialkyl phosphonates are bound to the metal atom via the phosphoryl (P = O) oxygen and the effectiveness of coordination depends upon the donor strength of the ligand and the environment of the cen

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6

Mahmoudpour, Asiyeh, Shohreh Nafisi, Ezzatollah Najafi, and Behrouz Notash. "Synthesis, characterization and electroluminescence properties of a new mixed-ligand diorganotin(IV) complex." Main Group Metal Chemistry 42, no. 1 (2019): 51–59. http://dx.doi.org/10.1515/mgmc-2019-0005.

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Abstract A new mixed-ligand diorganotin(IV) complex, [μ-(4-dpe){Me2Sn(cup)2}2] (1), was synthesized by reacting dimethyltin(IV) dichloride with 1,2-di(4-pyridyl)ethylene (4-dpe) and ammonium N-Nitroso-N-phenylhydroxylamine (cup). The prepared complex was fully characterized by PXRD, 1H, 13C and 119Sn NMR, IR, and UV spectra and elemental analysis (CHN). The structural analysis of complex 1 by X-ray diffraction showed that this compound consists of centrosymmetric binuclear units that crystallize in the monoclinic system with the space group of P21/c. Thermal behavior of this complex was interr

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7

Kumar, Amal K., and Tapas K. Chattopadhyay. "Catalytic role of diorganotin dichloride in esterification of carboxylic acids." Tetrahedron Letters 28, no. 32 (1987): 3713–14. http://dx.doi.org/10.1016/s0040-4039(00)96364-0.

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8

Dey, Dilip Kumar, Brajagopal Samanta, Antonin Lycka, and Lutz Dahlenburg. "Simple Synthesis, Characterization and Structure of Diorganotin(IV) Complexes Containing the N-(2-Salicylidene)-N'-benzoylhydrazone Ligand." Zeitschrift für Naturforschung B 58, no. 4 (2003): 336–44. http://dx.doi.org/10.1515/znb-2003-0415.

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Two diorganotin(IV) complexes of general formula R2Sn[2-OC6H4CH=NDN=C(O)Ph] (R = Ph, 1; R = Me, 2) have been synthesized from the corresponding diorganotin(IV) dichloride and the Schiff base derived from salicylaldehyde and benzoyl hydrazide. The two compounds have been characterized by elemental analysis, IR and NMR (1H, 13C, 15N, 119Sn) spectra, and their structures have been confirmed by single crystal X-ray structure analysis. Crystals of complex 1 re triclinic, space group P1̄ , a = 11.1631(5), b = 13.462(2), c = 16.511(1) Å , α = 106.193(9), β = 106.379(8), γ = 94.932(8)°, Z = 4, R1 = 0.

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9

Ee Khoo, Lian, Yan Xu, Ngoh Khang Goh, Lian Sai Chia, and Lip Lin Koh. "Molecular adducts of diorganotin dichloride with N-(2-oxidoarylideneaminoacidato) diorganotin(IV) complexes. Crystal structure of [Ph2Sn(2-OC10H6CH-NCH2COO)]SnPh2Cl2." Polyhedron 16, no. 4 (1997): 573–76. http://dx.doi.org/10.1016/0277-5387(96)00334-8.

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10

Tamas, Melinda, Roxana A. Butuza, Monica Dan, and Anca Silvestru. "Diorganotin(IV) Complexes of Organoselenolato Ligands with Pyrazole Moieties—Synthesis, Structure and Properties." Molecules 30, no. 7 (2025): 1648. https://doi.org/10.3390/molecules30071648.

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Diorganotin(IV) compounds of types RR′Sn(SeCH2CH2pz)2 [R = R′ = nBu (2), Ph (3); R = 2-(Me2NCH2)C6H4, R′ = Me (4), nBu (5), Ph (6)], and RR′SnX(SeCH2CH2pz) [R = 2-(Me2NCH2)C6H4, R′ = nBu, X = Cl (7), R′ = Me, X = SCN (9)], as well as [2-(Me2NCH2)C6H4](Me)Sn(NCS)2 (8), and the tin(II) Sn(SeCH2CH2pz)2 (10) (pz = pyrazole), were prepared by salt metathesis reactions between the appropriate diorganotin(IV) dichloride or dipseudohalide and Na[SeCH2CH2pz], with the latter freshly prepared from (pzCH2CH2)2Se2 (1). The solution behaviour of these compounds was investigated by multinuclear NMR (1H, 13C

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11

Sharma, Arti, Asha Jain, and Sanjiv Saxena. "Diorganotin(IV) complexes of flexible N-protected amino acids and ketoximes: preparation and structure – antimicrobial activity relationship." Canadian Journal of Chemistry 94, no. 2 (2016): 155–62. http://dx.doi.org/10.1139/cjc-2015-0126.

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Diorganotin(IV) complexes of flexible N-protected amino acids and ketoximes having the compositions Me2Sn [[Formula: see text]CHRCOO][ON = C6H10] (where R = –CH2CH(CH3)2, –CH(CH3)C2H5,–CH2C6H5, –CH(CH3)2) and Me2Sn[[Formula: see text]CHRCOO][ON=CR′R″] (where R = –CH2CH(CH3)2, –CH(CH3)C2H5, –CH2C6H5, R′ = R″ = CH3; R = –CH(CH3)C2H5, –CH2C6H5, –CH(CH3)2, R′ = CH3, R″ = C6H5) were prepared by the reaction of dimethyltin(IV) dichloride with sodium salts of flexible N-protected amino acids and ketoximes in 1:1:1 molar ratio in refluxing dry benzene. The synthesized complexes were characterized by e

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12

Shankar, Ravi, Meenal Asija, Nisha Singla, Gabriele Kociok-Köhn, and Kieran C. Molloy. "Synthesis, characterization and hydrolytic stability of diorganotin(IV)bis(O-alkyl alkylphosphonate)s." Canadian Journal of Chemistry 92, no. 6 (2014): 549–55. http://dx.doi.org/10.1139/cjc-2013-0486.

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Diorganotinbis(O-alkyl alkylphosphonate)s, R2Sn(O2P(OR1)R1)2 [R1 = Me, R = Me (1), Et (2), n-Bu (3); R1 = Et, R = Me (4), Et (5), n-Bu (6)] have been synthesized from the reaction between dimethyl/diethyl/di-n-butyltin dichloride and dialkyl alkylphosphonates, (R1O)2P(O)R1, in a solvent-free medium (120 °C, 18 h). X-ray crystal structure of 1 reveals two independent molecules in the unit cell that form one-dimensional polymeric motifs by virtue of bridging bidentate phosphonate groups. The structural attribute of each polymeric chain represents an orderly infinite array of -[Sn-O-P-O-]2 8-memb

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13

Amin, Nur Adibah Mohd, Rusnah Syahila Duali Hussen, See Mun Lee, Kae Shin Sim та Suerialoasan Navanesan. "Synthesis, structural characterization, cytotoxicity and encapsulation studies of N,Nʹ-(1, 2-dicyano-1,2-vinylene)-bis(4-hydroxysalicylideneaminato) di(p-chlorobenzyl)tin as potential anticancer drug". Main Group Metal Chemistry 42, № 1 (2019): 94–101. http://dx.doi.org/10.1515/mgmc-2019-0010.

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Abstract Two new diorganotin(IV) complexes with the general formula (RC7H6)2Sn(L) (where RC7H6 = p-ClBn, C1; and p-FBn, C2) were prepared based on the reaction of 2,3-bis(4-hydroxysalicylidene-amino)-maleic nitrile (L) with substituted dibenzyltin(IV) dichloride. The structures were confirmed by elemental analysis, Fourier transform infrared (FT-IR), proton and carbon nuclear magnetic resonance (1H and 13C NMR). They were tested against several cancer cell lines by using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. C1, which was most effective against MCF-7 bre

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14

Singh, Neetu, Subrato Bhattacharya, Heinrich Nöth, and Peter Mayer. "Synthesis, Characterization and Reactivity of a Diorganotin Thiocarboxylate: Dimethyl(thioacetato)-tin(IV) Chloride and its Reactions with Nucleophiles Exhibiting Desulfurization." Zeitschrift für Naturforschung B 64, no. 1 (2009): 116–22. http://dx.doi.org/10.1515/znb-2009-0116.

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Dimethyl(thioacetato)tin chloride (1) was synthesized by the reaction of dimethyltin dichloride with thioacetic acid in the presence of triethylamine. Compound 1 was subjected to hydrolysis under different reaction conditions in order to obtain sulfido/hydrosulfidotin compounds. Except for one case where the product was hexamethyl-1,3,5-trithia-2,4,6-tristannacyclohexane, (Me2SnS)3 (4), all other reactions led to desulfurization, and the products obtained were organostannoxane compounds, dinuclear tetramethyl-oxo-dichloroditin, {Me2SnCl2.Me2SnO}2 (2), and tetraacetatodioxotetra( dimethyltin),

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15

El-Sherif, Ahmed A., M. R. Shehata, Mohamed M. Shoukry, and N. Mahmoud. "Potentiometric Study of Speciation and Thermodynamics of Complex Formation Equilibria of Diorganotin(IV) Dichloride with 1-(2-Aminoethyl)piperazine." Journal of Solution Chemistry 45, no. 3 (2016): 410–30. http://dx.doi.org/10.1007/s10953-016-0450-5.

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16

Ma, Chunlin, Yinfeng Han, and Rufen Zhang. "Investigation on the coordination modes: Syntheses, characterization and crystal structures of diorganotin (IV) dichloride with 4(5)-imidazoledithiocarboxylic acid." Inorganica Chimica Acta 358, no. 11 (2005): 3084–92. http://dx.doi.org/10.1016/j.ica.2005.03.053.

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17

Momeni, Badri Z., Nastaran Fathi, Milad Moghadasi, Abbas Biglari та Jan Janczak. "New insight into the reactions of organoplatinum(II) complexes with diorganotin dichloride and diisothiocyanate: Oxidative addition, reductive elimination and α-elimination". Journal of Organometallic Chemistry 880 (лютий 2019): 368–77. http://dx.doi.org/10.1016/j.jorganchem.2018.11.022.

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18

Bonire, Josiah J., G. Adefikayo Ayoko, Philip F. Olurinola, Joseph O. Ehinmidu, Neelam S. N. Jalil, and Andrew A. Omachi. "Synthesis and Antifungal Activity of Some Organotin(IV) Carboxylates." Metal-Based Drugs 5, no. 4 (1998): 233–36. http://dx.doi.org/10.1155/mbd.1998.233.

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Six diorganotin(IV) carboxylates prepared by reacting diorganotin(IV) dichlorides with the respective silver carboxylate have been tested for antifungal activity against Aspergillus. niger, Aspergilluus flavus and Pencillium. citrinum in Sabourand dextrose broth. The compounds generally exhibit greater fungitoxicity than the diorganotin(IV) dichlorides and the carboxylic acids from which they were synthesized. In keeping with the generally accepted notion that the organotin moiety plays an important role in deciding the antifungal activity of an organotin compound, the diphenyltin(IV) compound

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19

Girasolo, M. Assunta, Domenico Schillaci, Clelia Di Salvo, Giampaolo Barone, Arturo Silvestri, and Giuseppe Ruisi. "Synthesis, spectroscopic characterization and in vitro antimicrobial activity of diorganotin(IV) dichloride adducts with [1,2,4]triazolo-[1,5-a]pyrimidine and 5,7-dimethyl-[1,2,4]triazolo-[1,5-a]pyrimidine." Journal of Organometallic Chemistry 691, no. 4 (2006): 693–701. http://dx.doi.org/10.1016/j.jorganchem.2005.10.007.

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20

Bengtson, Annemette, Ngoh Khang Goh, Alan Hazell, et al. "Reactions of 8-Aminoquinoline with Diorganotin Dichlorides." Acta Chemica Scandinavica 50 (1996): 1020–24. http://dx.doi.org/10.3891/acta.chem.scand.50-1020.

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21

El‐Khaldy, Adnan A. S. "Monothiophosphorylation of Diorganotin Dichlorides. Synthesis and Characterization." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 33, no. 2 (2003): 183–94. http://dx.doi.org/10.1081/sim-120017778.

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22

Turek, Jan, Zdeňka Padělková, Mikhail S. Nechaev, and Aleš Růžička. "Reduction of C,N-chelated Diorganotin(IV) Dichlorides." Journal of Organometallic Chemistry 695, no. 15-16 (2010): 1843–47. http://dx.doi.org/10.1016/j.jorganchem.2010.04.019.

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23

Whitesell, James K., and Richard Apodaca. "Trimethylsilylcyanation of aldehydes and ketones catalyzed by diorganotin dichlorides." Tetrahedron Letters 37, no. 15 (1996): 2525–28. http://dx.doi.org/10.1016/0040-4039(96)00386-3.

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24

WHITESELL, J. K., and R. APODACA. "ChemInform Abstract: Trimethylsilylcyanation of Aldehydes and Ketones Catalyzed by Diorganotin Dichlorides." ChemInform 27, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199629055.

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25

Zahra, Asadi, Asadi Mozaffar, and Khoshkharam Soror. "Thermodynamic studies of adduct formation reactions between organotin(IV)dichlorides and NiII macrocycles." Journal of Indian Chemical Society Vol. 91, May 2014 (2014): 813–22. https://doi.org/10.5281/zenodo.5719986.

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Chemistry Department, College of Sciences, Shiraz University, Shiraz, I.R. Iran <em>E-mail</em> : zasadi@susc.ac.ir, zasadi@shirazu.ac.ir Fax : 98-711-2286008 <em>Manuscript received online 15 October 2013, revised 17 October 2013, accepted 24 October 2013</em> This article presents σ-acceptor strength for the diorganotin(IV)dichlorides : dimethyltindichloride, diphenyltindichloride and dibutyltindichloride as Lewis acids toward some macrocyclic nickel(II) complexes. Thermodynamic of the adducts formation of the tin(IV)dichlorides with Ni(II)tetraaza Schiff base complexes such as : [Ni(M

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26

Chandrasekhar, Vadapalli, Ramalingam Thirumoorthi, Ramesh K. Metre, and Bani Mahanti. "Steric control in the reactions of 3-pyrazolecarboxylic acid with diorganotin dichlorides." Journal of Organometallic Chemistry 696, no. 2 (2011): 600–606. http://dx.doi.org/10.1016/j.jorganchem.2010.09.032.

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27

Ettorre, Renato, Daniele Marton, Luca Nodari, and Umberto Russo. "Coordination polymers formed by diorganotin dichlorides with 2,5-bis(4-pyridyl)-1,3,4-thiadiazole." Journal of Organometallic Chemistry 691, no. 4 (2006): 805–8. http://dx.doi.org/10.1016/j.jorganchem.2005.09.054.

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28

Ouyang, Jiexiang, Yan Xu, and Lian Ee Khoo. "Reactions of 8-methoxyquinoline [C10H9ON] and diorganotin dichlorides. Crystal structures of [C10H9ON·H]2Ph2SnCl4 and [C10H9ON·H·NOH9C10]Ph2SnCl3." Journal of Organometallic Chemistry 561, no. 1-2 (1998): 143–52. http://dx.doi.org/10.1016/s0022-328x(98)00509-9.

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29

Asadi, Mozaffar, Khosrow Aein Jamshid, and Ali Hossein Kyanfar. "Nickel(II) salophen-type complexes characterization and their thermodynamic studies with diorganotin(IV) dichlorides in chloroform." Transition Metal Chemistry 32, no. 6 (2007): 822–27. http://dx.doi.org/10.1007/s11243-007-0272-9.

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30

Momeni, B. Z., R. Kia, and S. Ghanbarzadeh. "Reactivity of diorganotin(IV) dichlorides towards N, P, and O donor ligands: crystal structure of [SnMe2Cl2(phendione)]." Monatshefte für Chemie - Chemical Monthly 143, no. 11 (2012): 1479–86. http://dx.doi.org/10.1007/s00706-012-0733-5.

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31

Sedaghat, Tahereh, and Saied Menati. "Synthesis and spectroscopic characterization of new adducts of diorganotin(IV) dichlorides with an asymmetric schiff base ligand." Inorganic Chemistry Communications 7, no. 6 (2004): 760–62. http://dx.doi.org/10.1016/j.inoche.2004.04.003.

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32

Asadi, Mozaffar, Khosrow Aein Jamshid, and Ali Hossein Kyanfar. "Thermodynamic Studies of the Interaction of Nickel(II) Schiff Base Complexes with Diorganotin (IV) Dichlorides in Non‐Aqueous Solvents." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 37, no. 2 (2007): 77–83. http://dx.doi.org/10.1080/15533170601187391.

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33

Asadi, Zahra, Mozaffar Asadi, and Fatemeh Mosalanezhad. "The Interaction of Nickel(II) and Copper(II) Schiff Base Complexes with Diorganotin(IV) Dichlorides in Acetonitrile: A Thermodynamic Study." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 41, no. 9 (2011): 1158–66. http://dx.doi.org/10.1080/15533174.2011.591362.

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34

Aein Jamshid, Khosrow, Mozaffar Asadi, and Ali Hossein Kianfar. "Synthesis, characterization and thermal studies of dinuclear adducts of diorganotin(IV) dichlorides with nickel(II) Schiff-base complexes in chloroform." Journal of Coordination Chemistry 62, no. 7 (2009): 1187–98. http://dx.doi.org/10.1080/00958970802363974.

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35

Azadbakht, Azadeh, Mohammad Bagher Gholivand, and Saeid Menati. "Nanomolar detection of hydrogen peroxide at a nano-structured adducts of diorganotin dichlorides multiwall carbon nanotube modified glassy carbon electrode." Electrochimica Acta 78 (September 2012): 82–91. http://dx.doi.org/10.1016/j.electacta.2012.05.160.

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36

Buntine, Mark A., Frances J. Kosovel, and Edward R. T. Tiekink. "Supramolecular Sn⋯Cl associations in diorganotin dichlorides and their influence on molecular geometry as studied by ab initio molecular orbital calculations." CrystEngComm 5, no. 58 (2003): 331–36. http://dx.doi.org/10.1039/b308922c.

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37

Asadi, Mozaffar, Zahra Asadi, and Fatemeh Mosalanezhad. "Synthesis, kinetics, and mechanism for adduct formation of tetraaza Schiff base cobalt(II) complexes with diorganotin(IV)dichlorides in dimethylformamide solvent." International Journal of Chemical Kinetics 42, no. 8 (2010): 499–507. http://dx.doi.org/10.1002/kin.20499.

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38

Asadi, Z., M. Asadi, and F. Mosalanezhad. "Kinetics, mechanism and synthesis of adduct formation of tetraaza Schiff base cobalt(II) complexes as donor with diorganotin(IV)dichlorides as acceptor." Journal of the Iranian Chemical Society 8, no. 3 (2011): 794–802. http://dx.doi.org/10.1007/bf03245910.

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39

Asadi, Mozaffar, Khosrow Aein Jamshid, and Ali Hossein Kyanfar. "Synthesis, characterization and equilibrium study of the dinuclear adducts formation between nickel(II) Salen-type complexes with diorganotin(IV) dichlorides in chloroform." Inorganica Chimica Acta 360, no. 5 (2007): 1725–30. http://dx.doi.org/10.1016/j.ica.2006.09.013.

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40

Sousa, Gerimário F. de, Javier Ellena, Valéria R. S. Malta, and José D. Ardisson. "Different coordination modes for disulfoxides towards diorganotin(IV) dichlorides. X-ray crystal structures of 1,2-cis-bis-(phenylsulfinyl)ethene (rac-,cis-cbpse) and adducts [{Ph2SnCl2(meso-bpse)}n] and [{n-Bu2SnCl2(pdtd)}2]." Journal of the Brazilian Chemical Society 20, no. 8 (2009): 1441–47. http://dx.doi.org/10.1590/s0103-50532009000800008.

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41

Sharma, Shobhita, Shobhana Sharma, Shiv Om Meena, and Manish Vashishtha. "Efficacy of Radical‐Scavenging Activity in Novel Diorganotin(IV) Complexes of Schiff Bases of Salicylaldehyde." ChemistrySelect 9, no. 40 (2024). http://dx.doi.org/10.1002/slct.202404204.

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AbstractBiopotent hybrid diorganotin(IV) complexes, derived from salicylaldehyde Schiff bases having general formula R2SnL, where LH = (OH)C6H4HC: NCR′(R″)CHR‴OH] [where R = Me or Bu], were logically designed, generated, and characterized using spectroscopic techniques, single‐crystal X‐ray investigations, and DFT studies. Different diorganotin(IV) complexes were synthesized because of interaction between diorganotin(IV) dichloride and sodium salts of Schiff bases of salicylaldehyde ligand in anhydrous refluxing THF at 1:1 and 1:2 molar ratio (Product A and B). The chelating property of Schiff

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42

KUMAR, A. K., and T. K. CHATTOPADHYAY. "ChemInform Abstract: Catalytic Role of Diorganotin Dichloride in Esterification of Carboxylic Acids." ChemInform 19, no. 2 (1988). http://dx.doi.org/10.1002/chin.198802104.

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43

Kumar, Manoj, Priyanka siwach, Harish Sharma, et al. "New Schiff Base Derived Organotin (IV) Complexes: Synthesis, Characterization, In vitro and In silico Biological Studies." Anti-Infective Agents 22 (April 26, 2024). http://dx.doi.org/10.2174/0122113525305623240409075331.

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Aims: The creation and testing of new Schiff base-based antibacterial organotin (IV) complexes were the objectives of this investigation. background: Due to developed resistance, antibiotics that were once often used to treat microorganisms are no longer effective against them. It is thought that organotin compounds synthesized from Schiff bases have significant pharmacological effectiveness and work well as antibacterial agents Background: Due to developed resistance, antibiotics that were once often used to treat microor-ganisms are no longer effective against them. It is thought that organo

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