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Journal articles on the topic 'Diorganotin'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Ryyis Arraq, Rafid, Hadeer Jasem, and Angham G. Hadi G. Hadi. "Synthesis, evaluation, and structural characterization of antioxidant diorganotin(IV) Complexes derived from ampicillin: a comprehensive study." Bulletin of the Chemical Society of Ethiopia 38, no. 5 (2024): 1291–300. http://dx.doi.org/10.4314/bcse.v38i5.8.

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This study offerings the preparation, structural analysis, and estimation of novel diorganotin(IV) complexes derived from an ampicillin as a ligand in terms of their antioxidant activity. The diorganotin complexes were yielded by a direct reaction between ampicillin and a different number of diorganotin(IV) chloride precursors. Various spectroscopic techniques, including CHNS, FTIR and nuclear magnetic resonance (1H, 13C, 119Sn NMR), were used to explain the molecular structures of the produced complexes. Through in vitro experiments such as the CUPRAC and DPPH (2,2-diphenyl-1-picrylhydrazyl)

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2

Hadi, Angham G., Emad Yousif, Gamal A. El-Hiti, et al. "Long-Term Effect of Ultraviolet Irradiation on Poly(vinyl chloride) Films Containing Naproxen Diorganotin(IV) Complexes." Molecules 24, no. 13 (2019): 2396. http://dx.doi.org/10.3390/molecules24132396.

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As poly(vinyl chloride) (PVC) photodegrades with long-term exposure to ultraviolet radiation, it is desirable to develop methods that enhance the photostability of PVC. In this study, new aromatic-rich diorganotin(IV) complexes were tested as photostabilizers in PVC films. The diorganotin(IV) complexes were synthesized in 79–86% yields by reacting excess naproxen with tin(IV) chlorides. PVC films containing 0.5 wt % diorganotin(IV) complexes were irradiated with ultraviolet light for up to 300 h, and changes within the films were monitored using the weight loss and the formation of specific fu

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3

Yadav, Jyoti, and Jai Devi. "Antimicrobial and Antioxidant Activities of Diorganotin(IV) Complexes Synthesized from 1,2,4-Triazole Derivatives." Asian Journal of Chemistry 32, no. 10 (2020): 2553–58. http://dx.doi.org/10.14233/ajchem.2020.22819.

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Novel diorganotin(IV) complexes were synthesized from 1,2,4-triazole Schiff base ligands which were synthesized by reaction between the 4-amino-5-phenyl-1,2,4-triazole-3-thiol and salicyaldehyde derivatives. The bonding and geometry of the diorganotin(IV) complexes were evaluated by using different spectroscopic techniques such as FT-IR, mass, 1H, 13C & 119Sn NMR. The different spectroscopic techniques revealed the tridentate (ONS) mode of chelation of Schiff base ligands and pentacoordinated environment around the central tin metal which was satisfied with azomethine nitrogen, phenolic ox

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4

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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5

López-Cardoso, Marcela, Cristina Rodríguez-Narváez, Gabriela Vargas-Pineda, et al. "Synthesis, spectroscopic characterization and crystal structures of diorganotin (IV) complexes of 2-N-propyl and 2-N-benzyl-amino-1-cyclopentene-1-carbodithioates." Main Group Metal Chemistry 38, no. 1-2 (2015): 1–8. http://dx.doi.org/10.1515/mgmc-2014-0019.

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6

Ali, Saqib, Muhammad Danish, and Muhammad Mazhar. "Redistribution reactions of diorganotin dicarboxylates and diorganotin dihalides: A convenient method for the preparation of halo-diorganotin carboxylates." Heteroatom Chemistry 8, no. 3 (1997): 273–78. http://dx.doi.org/10.1002/(sici)1098-1071(1997)8:3<273::aid-hc11>3.0.co;2-o.

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7

Reuter, Hans, and Martin Reichelt. "Reaction products of diorganotin(IV) oxides, R2SnO, with nitric acid. Part 2 – R = n-butyl and t-butyl." Canadian Journal of Chemistry 92, no. 6 (2014): 484–95. http://dx.doi.org/10.1139/cjc-2013-0514.

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The reaction of diorganotin(IV) oxides, R2SnO with R = n-butyl and t-butyl, with nitric acid in different stoichiometric ratios resulted in the formation of different products depending on the organic groups attached to the tin atom: the diorganotin(IV) dinitrate dihydrates, n-Bu2Sn(NO3)2·2H2O (2d) and t-Bu2Sn(NO3)2·2H2O (2e), the mixed diorganotin(IV) nitrate methoxide oxide n-Bu2Sn(NO3)(n-Bu2SnOMe)O (6), and the diorganotin(IV) nitrate hydroxide hydrate t-Bu2Sn(NO3)(OH)·H2O = [t-Bu2Sn(OH)(H2O)][NO3] (7). On examination of the solubility of the primary reaction products in different solvents,

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8

T., N. SRIVASTAVA, and A. SIDDIQUI M. "Some Semlcarbazone Derivatives of Diorganotin(Iv)." Journal of Indian Chemical Society Vol. 64, Aug 1987 (1987): 500–501. https://doi.org/10.5281/zenodo.6200742.

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9

Yadav, Shipra, Imtiyaz Yousuf, Mohammad Usman, Musheer Ahmad, Farukh Arjmand, and Sartaj Tabassum. "Synthesis and spectroscopic characterization of diorganotin(iv) complexes of N′-(4-hydroxypent-3-en-2-ylidene)isonicotinohydrazide: chemotherapeutic potential validation by in vitro interaction studies with DNA/HSA, DFT, molecular docking and cytotoxic activity." RSC Advances 5, no. 63 (2015): 50673–90. http://dx.doi.org/10.1039/c5ra06953j.

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10

Singh, Pooja, Amita Singh, Ayushi Singh, et al. "New 1D diorganotin(iv) dithiolate coordination polymers: crystallographic, computational, Hirshfeld surface and thermal analyses." CrystEngComm 22, no. 11 (2020): 2049–59. http://dx.doi.org/10.1039/c9ce01917k.

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11

Roy, Manojit, Subhadip Roy, Keisham Surjit Singh, Janmoni Kalita, and S. Sureshkumar Singh. "Synthesis, characterization and anti-diabetic assay of diorganotin(iv) azo-carboxylates: crystal structure and topological studies of azo-dicarboxylic acid ligand and its cyclic tetranuclear dimethyltin(iv) complex." New Journal of Chemistry 40, no. 2 (2016): 1471–84. http://dx.doi.org/10.1039/c5nj02637g.

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12

Shang, Xianmei, Bin Zhao, Guangya Xiang, M. Fátima C. Guedes da Silva та Armando J. L. Pombeiro. "Dimeric diorganotin(iv) complexes with arylhydrazones of β-diketones: synthesis, structures, cytotoxicity and apoptosis properties". RSC Advances 5, № 56 (2015): 45053–60. http://dx.doi.org/10.1039/c5ra06658a.

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13

SANGEETA, BHARGAVA, AGIWAL MANJU, JAIN SUNITA, T. PARDASANI R., and SINGH PAHUP. "Diorganotin(Iv) Chelates of naturally occurring Hydroxynaphthoquinones." Journal of Indian Chemical Society Vol. 70, Mar 1993 (1993): 234–36. https://doi.org/10.5281/zenodo.5917557.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 <em>Manuscript received 6 September 1991, revised 23 April 1992, accepted 12 November 1992</em> Diorganotin(Iv) Chelates of naturally occurring Hydroxynaphthoquinones

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14

Smith, Frank E., Lian Ee Khoo, Ngoh Khang Goh, Rosemary C. Hynes, and George Eng. "The synthesis, and molecular and crystal structure of diphenyl(2-oxidonaphthylmethyl-iminoacetato)tin(IV)." Canadian Journal of Chemistry 74, no. 11 (1996): 2041–47. http://dx.doi.org/10.1139/v96-233.

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The new diorganotin complex ((C6H5)2Sn(OC10H6CH=NCH2COO)) was prepared and characterized by 1H NMR, IR, elemental analysis, and a single crystal X-ray diffraction study. The crystals are monoclinic, space group P21/a with a = 16.9167(9) Å, b = 19.1276(16) Å, c = 26.538(2) Å, β = 100.534(6)°, V = 8442.5(11) Å3, Z = 16, and Dcalc = 1.574 Mg m−3. The final discrepancy factors are RF = 0.030, and RW = 0.021 for 6524 significant reflections. The tin atom has a distorted trigonal bipyramidal coordination, with no short intermolecular contacts. The two axial Sn—O bonds of 2.12 Å and 2.09 Å and the eq

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15

Schmiedgen, Ralf, Friedo Huber, Arturo Silvestri, Giuseppe Ruisi, Mario Rossi, and Renato Barbieri. "Diorganotin(IV)-2-mercaptopyrimidine complexes." Applied Organometallic Chemistry 12, no. 12 (1998): 861–71. http://dx.doi.org/10.1002/(sici)1099-0739(199812)12:12<861::aid-aoc819>3.0.co;2-0.

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16

Wrackmeyer, Bernd, Gerald Kehr та Roland Boese. "π-Coordination of Diorganotin Dications". Angewandte Chemie International Edition in English 30, № 10 (1991): 1370–72. http://dx.doi.org/10.1002/anie.199113701.

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17

Tang, Liang-Fu, Pei-Juan Zhu, and Ji-Tao Wang. "Synthesis and Crystal Structure of Diorganotin(IV) Derivatives Containing the bis(3,5-dimethylpyrazol-1-yl) Acetate Ligand." Journal of Chemical Research 2002, no. 8 (2002): 370–71. http://dx.doi.org/10.3184/030823402103172536.

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Two new diorganotin(IV) derivatives containing the heteroscorpionate ligand have been synthesised by reaction of diphenyltin halides with bis(3,5-dimethylpyrazol-1-yl)acetate lithium and have been characterised by X-ray analysis.

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18

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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19

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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20

Dakternieks, Dainis, Bernhard Zobel, Klaus Jurkschat, Marcus Schürmann, and Edward R. T. Tiekink. "A Spacer-Linked Molecular Diorganotin Oxide." Organometallics 22, no. 6 (2003): 1343–45. http://dx.doi.org/10.1021/om020749d.

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21

Mundorff, E., F. Caruso, A. Cingolani, F. Marchetti, C. Pettinari та M. Rossi. "Diorganotin complexes of β-diketonate ligands". Acta Crystallographica Section A Foundations of Crystallography 52, a1 (1996): C291. http://dx.doi.org/10.1107/s0108767396087880.

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22

Jiménez-Pérez, Víctor M., Henrich Nöth, Armando Ariza-Castolo, Angelina Flores-Parra, and Rosalinda Contreras. "Optically active pentacyclic binuclear diorganotin compounds." Journal of Organometallic Chemistry 691, no. 8 (2006): 1584–89. http://dx.doi.org/10.1016/j.jorganchem.2005.11.072.

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23

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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24

Mokal, Vijaya B., and Vimal K. Jain. "Diorganotin(IV) Dialkoxyphosphinothioates: Synthesis and Characterization." Bulletin of the Chemical Society of Japan 68, no. 4 (1995): 1149–54. http://dx.doi.org/10.1246/bcsj.68.1149.

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25

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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26

Das, Mrinal K., Matilal Nath, and Somnath De. "Synthesis and Ligand Exchange Reaction of Some Organotin(IV) Bis(N-arylsulphonyl-N-arylhydroxylaminates)." Zeitschrift für Naturforschung B 48, no. 2 (1993): 185–88. http://dx.doi.org/10.1515/znb-1993-0209.

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AbstractSeveral diorganotin(IV)-bis(N-arylsulphonyl-N-arylhydroxylaminates) of the general formula R2Sn[ON(R1)SO2R2]2 have been synthesized and characterized by elemental analyses and by IR and 1H NMR spectra. A representative ligand exchange reaction with N-benzoyl- N-phenylhydroxylamine has been carried out.

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27

J., C.TREHAN, R.K.SHARMA, KUMAR N., P. SHARMA C., S. GARG B. та P. SINGH R. "Spectroscopic Studies of some New Diorganotin(IV)- β-diketonate Complexes". Journal of Indian Chemical Society Vol. 62, Oct 1985 (1985): 777–78. https://doi.org/10.5281/zenodo.6324692.

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National Physical Laboratory, Hillside Road, New Delhi-110 012 Department of Chemistry, University of Delhi, Delhi-110 007 <em>Manuscript received 26 June 1984, revised 30 April 1985, accepted 29 October 1985</em> Spectroscopic Studies of some New Diorganotin(IV)- <em>β</em>-diketonate Complexes  

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28

Xie, Yun-Peng, Jian-Fang Ma, Jin Yang, and Min-Zhong Su. "Monoorganooxotin cage, diorganotin ladders, diorganotin double chain and triorganotin single chain formed with phosphonate and arsonate ligands." Dalton Trans. 39, no. 6 (2010): 1568–75. http://dx.doi.org/10.1039/b915255e.

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29

Wiecek, Joanna, Dimitra Kovala-Demertzi, Zbigniew Ciunik, Maria Zervou, and Mavroudis A. Demertzis. "Diorganotin Complexes of a Thiosemicarbazone, Synthesis: Properties, X-Ray Crystal Structure, and Antiproliferative Activity of Diorganotin Complexes." Bioinorganic Chemistry and Applications 2010 (2010): 1–9. http://dx.doi.org/10.1155/2010/867195.

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The synthesis and spectral characterization of novel diorganotin complexes with 3-hydroxypyridine-2-carbaldehyde thiosemicarbazone,(1), [(L)](2), [(L)](3), and [(L)](4)are reported. The single-crystal X-ray structure of complex [(L)(DMSO)](5)shows that the ligand is doubly deprotonated and is coordinated as tridentate ligand. The six coordination number is completed by two carbon atoms of phenyl groups. There are two similar monomers5a(Sn1) and5b(Sn51) in the asymmetric unit. The monomers5aand5bare linked through intermolecular hydrogen bonds of N–H–O and C–H–S type. , intermolecular interacti

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30

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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31

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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32

Lee, See Mun, H. Mohd Ali, and Kong Mun Lo. "Synthesis, structures and characterization of diorganotin complexes." Acta Crystallographica Section A Foundations of Crystallography 66, a1 (2010): s271. http://dx.doi.org/10.1107/s0108767310093815.

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33

Shankar, Ravi, Archana Jain, Atul Pratap Singh, and Kieran C. Molloy. "Diorganotin Sulfonate and Phosphonate-Based Coordination Polymers." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 6 (2011): 1375–78. http://dx.doi.org/10.1080/10426507.2010.543110.

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34

Sandhu, G. K., S. Dass, and N. S. Boparoy. "Diorganotin(IV) Adducts with Amine N-Oxides." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 20, no. 4 (1990): 393–408. http://dx.doi.org/10.1080/00945719008048143.

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35

Sandhu, G. K., R. Gupta, S. S. Sandhu, L. S. Moore, and R. V. Parish. "Diorganotin(IV) complexes of N-protected dipeptides." Journal of Organometallic Chemistry 311, no. 3 (1986): 281–88. http://dx.doi.org/10.1016/0022-328x(86)80250-9.

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36

Lee, F. L., E. J. Gabe, L. E. Khoo, W. H. Leong, G. Eng, and F. E. Smith. "Synthesis and structural studies of diorganotin iminodiacetates." Inorganica Chimica Acta 166, no. 2 (1989): 257–61. http://dx.doi.org/10.1016/s0020-1693(00)80818-x.

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37

Sandhu, G. K., R. Gupta, S. S. Sandhu, and R. V. Parish. "Diorganotin(VI) complexes of N-acetylamino acids." Polyhedron 4, no. 1 (1985): 81–87. http://dx.doi.org/10.1016/s0277-5387(00)84226-6.

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38

Tiwari, Rashmi, G. Srivastava, R. C. Mehrotra, and A. J. Crowe. "Some new salicyldeneimine complexes of diorganotin(IV)." Inorganica Chimica Acta 111, no. 2 (1986): 167–70. http://dx.doi.org/10.1016/s0020-1693(00)84647-2.

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39

Chilwal, Asha, Gagan Deep, Priti Malhotra, and A. K. Narula. "Diorganotin complexes of carboxylates: synthesis and characterization." Journal of Coordination Chemistry 66, no. 6 (2013): 1046–57. http://dx.doi.org/10.1080/00958972.2013.775428.

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40

Yoder, Claude H., Dian Mokrynka, Suzanne M. Coley, et al. "Stoichiometry of diorganotin dihalide adducts in solution." Organometallics 6, no. 8 (1987): 1679–84. http://dx.doi.org/10.1021/om00151a012.

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41

Jiang, Wujiu, Yuxing Tan, and Yiyuan Peng. "Aroylhydrazone Diorganotin Complexes Causes DNA Damage and Apoptotic Cell Death: From Chemical Synthesis to Biochemical Effects." International Journal of Molecular Sciences 22, no. 24 (2021): 13525. http://dx.doi.org/10.3390/ijms222413525.

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Under microwave irradiation, eighteen new aroylhydrazone diorganotin complexes (1a–9b) were produced through the reaction of aroylhydrazine, 2-ketobutyric acid, and the corresponding diorganotin. Fourier transform infrared spectroscopy, 1H, 13C, and 119Sn nuclear magnetic resonance spectroscopies, high-resolution mass spectroscopy, X-ray crystallography, and thermogravimetric analysis (TGA) were performed to characterize the complexes. The in vitro anticancer activity for complexes were assessed using a CCK-8 assay on human cancer cells of HepG2, NCI-H460, and MCF-7. Complex 4b revealed more i

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42

Nath, Mala, and P. K. Saini. "Synthesis and Characterization of Nanometric Pure Phase SnO2 Obtained from Pyrolysis of Diorganotin(IV) Derivatives of Macrocycles." ISRN Nanomaterials 2012 (October 14, 2012): 1–7. http://dx.doi.org/10.5402/2012/769528.

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Thermal decomposition of diorganotin(IV) derivatives of macrocycles of general formula, R2Sn(L1) and R2Sn(L2) (where R = n-butyl (1/4), methyl (2/5), and phenyl (3/6); H2L1 = 5,12-dioxa-7,14-dimethyl-1,4,8,11-tetraazacyclotetradeca-1,8-diene and H2L2 = 6,14-dioxa-8,16-dimethyl-1,5,9,13-tetraazacyclotetradeca-1,9-diene), provides a simple route to prepare nanometric SnO2 particles. X-ray line broadening shows that the particle size varies in the range of 36–57 nm. The particle size of SnO2 obtained by pyrolysis of 3 and 5 is in the range of 5–20 nm as determined by transmission electron microsc

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43

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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44

Sandhu, G. K., and N. S. Boparoy. "Diorganotin(IV) Derivatives of Thiophene-2-carboxylic Acid." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 20, no. 7 (1990): 975–88. http://dx.doi.org/10.1080/00945719008048189.

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45

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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46

Rotar, Adina, Richard A. Varga, and Cristian Silvestru. "Substitutional disorder in a hypervalent diorganotin(IV) dihalide." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (2007): m45. http://dx.doi.org/10.1107/s1600536807063386.

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47

Rossi, Miriam, and Francesco Caruso. "Trans–cis octahedral interconversion pathway in diorganotin compounds." Journal of Organometallic Chemistry 691, no. 8 (2006): 1535–43. http://dx.doi.org/10.1016/j.jorganchem.2005.12.021.

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Kašná, Blanka, Roman Jambor, Libor Dostál, Ivana Císařová, and Jaroslav Holeček. "Double O,C,O-chelated diorganotin(IV) derivatives." Journal of Organometallic Chemistry 691, no. 8 (2006): 1554–59. http://dx.doi.org/10.1016/j.jorganchem.2005.12.030.

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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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Singh, Neetu, Subrato Bhattacharya, and Heinrich Nöth. "Synthesis and characterization of a diorganotin bis(thioacetate)." Journal of Molecular Structure 969, no. 1-3 (2010): 229–32. http://dx.doi.org/10.1016/j.molstruc.2010.02.043.

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