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Journal articles on the topic 'Di-n-butyltin(IV)'

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Published: 5 June 2025

Last updated: 1 August 2025

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1

da Silva, Mônica Araújo, Anderson Selton Silva dos Santos, Thatiane Veríssimo dos Santos, Mario Roberto Meneghetti, and Simoni Margareti Plentz Meneghetti. "Organotin(iv) compounds with high catalytic activities and selectivities in the glycerolysis of triacylglycerides." Catalysis Science & Technology 7, no. 23 (2017): 5750–57. http://dx.doi.org/10.1039/c7cy01559c.

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Sn(iv) complexes, i.e., di-n-butyltin dichloride, n-butyltin trichloride, di-n-butyltin dilaurate, n-butyl stannoic acid, and di-n-butyl-oxo-stannane, were tested as catalysts for the glycerolysis of triacylglycerides (TAGs) to produce monoacylglycerols (MAGs) and diacylglycerols (DAGs).

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2

Baba, Ibrahim, Nor Syaidatul Akmal, Normah Awang та Seik Weng Ng. "Bis(N-benzyl-N-isopropyldithiocarbamato-κS)di-n-butyltin(IV)". Acta Crystallographica Section E Structure Reports Online 65, № 5 (2009): m595. http://dx.doi.org/10.1107/s1600536809015116.

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3

Ballivet-Tkatchenko, Danielle, Hélène Cattey, Laurent Plasseraud та Philippe Richard. "catena-Poly[[di-n-butyltin(IV)]-μ-trifluoromethanesulfonato-[[di-n-butyl(trifluoromethanesulfonato)tin(IV)]-di-μ-hydroxo]]". Acta Crystallographica Section E Structure Reports Online 62, № 11 (2006): m2820—m2822. http://dx.doi.org/10.1107/s160053680603964x.

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4

Weng Ng, Seik, V. G. Kumar Das, Wai-Hing Yip, Ru-Ji Wang, and Thomas C. W. Mak. "Di-n-butyltin(IV) di-o-bromobenzoate, a weakly-bridged dimer." Journal of Organometallic Chemistry 393, no. 2 (1990): 201–4. http://dx.doi.org/10.1016/0022-328x(90)80199-a.

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5

Narula, Suraj P., Shashi K. Bharadwaj, Yash Sharda, Roberta O. Day, Lori Howe, and Robert R. Holmes. "Dimeric structures of di-n-butyltin(IV) ortho-substituted dibenzoates." Organometallics 11, no. 6 (1992): 2206–11. http://dx.doi.org/10.1021/om00042a039.

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6

Sandeep, Pokharia, Joshi Rachana, Pokharia Mamta, Kumar Yadav Swatantra, and Mishra Hirdyesh. "Conceptual-DFT insights on the structure and reactivity of di-n-butyltin(IV) derivative of chlordiazepoxide." Journal of Indian Chemical Society Vol. 93, Sep 2016 (2016): 1053–65. https://doi.org/10.5281/zenodo.5639336.

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Organometallics and Molecular Modelling Group, Chemistry Section, Physics Section, M.M.V., Banaras Hindu University, Varanasi-221 005, Uttar Pradesh, India <em>E-mail </em>: sandeepp@bhu.ac.in Fax : 91-542-2367927 <em>Manuscript received online 17 January 2016, accepted 06 April 2016</em> The role of conceptual-DFT in understanding the structure and reactivity of <em>n</em>-Bu<sub>2</sub> SnL<sub>2</sub> , where L is the monoanion of chlordiazepoxide (LH), a benzodiazepine derivative with hypnotic action, have been highlighted using the Gaussian09 software package. The molecular geometries of

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7

Sadiq-ur-Rehman, Hanh Vien Ly, Saqib Ali, Amin Badshah та Masood Parvez. "Bis[2,3-bis(4-chlorophenyl)propenoato-κ2O:O′]di-n-butyltin(IV)". Acta Crystallographica Section E Structure Reports Online 60, № 8 (2004): m1144—m1146. http://dx.doi.org/10.1107/s1600536804017039.

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8

Win, Yip Foo, Teoh Siang Guan та Bohari M. Yamin. "Bis(2-amino-5-nitrobenzoato-κ2O,O′)di-n-butyltin(IV)". Acta Crystallographica Section E Structure Reports Online 62, № 1 (2005): m34—m36. http://dx.doi.org/10.1107/s1600536805039875.

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9

Holeček, J., M. Nádvorník, K. Handlíř, and A. Lyčka. "13C and 119Sn NMR spectra of Di-n-butyltin(IV) compounds." Journal of Organometallic Chemistry 315, no. 3 (1986): 299–308. http://dx.doi.org/10.1016/0022-328x(86)80450-8.

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10

Hong, Min, Yuanguang Yang, Chuan Li, Lidan Xu, Dacheng Li, and Chen-zhong Li. "Study of the effect of molecular structure and alkyl groups bound with tin(iv) on their cytotoxicity of organotin(iv) 2-phenyl-4-selenazole carboxylates." RSC Advances 5, no. 124 (2015): 102885–94. http://dx.doi.org/10.1039/c5ra18445b.

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Five organotin(iv) compounds Ph<sub>3</sub>SnL (1), (R<sub>2</sub>Sn)<sub>4</sub>O<sub>2</sub>L<sub>4</sub> [R = n-Bu (2), n-Oct (3)], (R<sub>2</sub>Sn)<sub>4</sub>O<sub>2</sub>L<sub>2</sub>Cl<sub>2</sub> [R = n-Bu (4), Me (5)], HL = 2-phenyl-4-selenazole carboxylic acid, were synthesized, of which triphenyl- and di-n-butyltin(iv) compounds display higher in vitro cytotoxicities.

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11

Reuter, Hans, та Coco K. Y. A. Okio. "Crystal structure of bis(benzoato-κO)dibutyltin(IV), nBu2Sn(bzo)2". Acta Crystallographica Section E Crystallographic Communications 72, № 7 (2016): 897–900. http://dx.doi.org/10.1107/s2056989016008604.

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The title compound, [Sn(C4H9)2(C6H5COO)2], was synthesized in order to study the interaction between di-n-butyltin(IV) oxide and some carboxylic acids. Di-n-butyltin(IV) dibenzoate, nBu2Sn(obz)2, exhibits the same structural features as other diorganotin(IV) dibenzoates characterized by an unsymmetrical bidentate bonding mode [Δ(Sn—O) ≃ 0.4 Å] of the two benzoate groups to tin. In a first approximation, the coordination sphere at tin resulting from the two stronger bonded O atoms [2.1227 (17) and 2.1405 (16) Å] and the two α-C atoms of then-butyl groups [2.125 (3) and 2.129 (2) Å] is compresse

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12

Devi, Sanasam Sachika, Manojit Roy, Subhadip Roy, and Keisham Surjit Singh. "Crystal structure and spectral characterization of di-n-butyltin(IV) compound of vanillin." Main Group Chemistry 14, no. 4 (2015): 339–48. http://dx.doi.org/10.3233/mgc-150176.

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13

Lyčka, A., and J. Holeček. "An 17O NMR study of some di- and tri-n-butyltin(IV) carboxylates." Journal of Organometallic Chemistry 294, no. 2 (1985): 179–82. http://dx.doi.org/10.1016/0022-328x(85)87467-2.

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14

Reichelt, Martin, та Hans Reuter. "catena-Poly[[di-tert-butyltin(IV)]-μ-oxalato]". Acta Crystallographica Section E Structure Reports Online 70, № 4 (2014): m133. http://dx.doi.org/10.1107/s160053681400539x.

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The title compound, [Sn(C4H9)2(C2O4)]n, an unexpected side product in the reaction of di-tert-butyltin(IV) oxide with nitric acid, represents the first diorganotin(IV) oxalate to be structurally characterized. The SnIVatom of the one-dimensional coordination polymer is located on a mirror plane and is coordinated by two chelating oxalate ions with two rather different Sn—O bond lengths of 2.150 (1) and 2.425 (1) Å, and twot-butyl groups with Sn—C bond lengths of 2.186 (2) and 2.190 (2) Å. The coordination polyhedron around the SnIVatom is a distorted tetragonal disphenoid. The centrosymmetric

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15

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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16

Plasseraud, Laurent, Hélène Cattey, and Philippe Richard. "Structural Characterization of 2,2-Di-n-butyl-4-methyl-1,3,2- dioxastannolane Isolated from Supercritical CO2 Conditions." Zeitschrift für Naturforschung B 64, no. 7 (2009): 831–34. http://dx.doi.org/10.1515/znb-2009-0710.

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The title compound has been isolated as single crystals from the synthesis of propylene carbonate from racemic 1,2-propanediol and carbon dioxide using n-Bu2SnO as a catalyst precursor. The X-ray crystallographic structure analysis revealed the self-assembly of di-n-butyltin(IV) 1,2-propanediolate units, linked together through long-distance Sn-O interactions leading to a one-dimensional polymeric architecture organized in a syndiotactic arrangement. The coordination geometry around the tin atoms can be described as an unusual faced-capped trigonal bipyramidal environment.

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17

Wang, Hongyun, та Handong Yin. "Di-μ3-oxido-bis(μ2-quinaldato-κ2O:O)bis(quinaldato-κ2N,O)tetrakis[di-n-butyltin(IV)]". Acta Crystallographica Section E Structure Reports Online 64, № 1 (2007): m197—m198. http://dx.doi.org/10.1107/s1600536807066378.

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18

Weng Ng, Seik, V. G. Kumar Das, Brian W. Skelton, and Allan H. White. "The tin(IV) coordination environment in di-n-butyltin di-p-bromobenzoate, a monomeric diorganotin ester." Journal of Organometallic Chemistry 377, no. 2-3 (1989): 221–25. http://dx.doi.org/10.1016/0022-328x(89)80083-x.

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19

Pokharia, Sandeep. "A Density Functional Theory (DFT) study on di-n-Butyltin(IV) Derivative of Glycyltryptophane." Asian Journal of Research in Chemistry 9, no. 2 (2016): 53. http://dx.doi.org/10.5958/0974-4150.2016.00010.9.

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20

He, H. B., X. L. Ge, and B. F. Ruan. "Synthesis, Crystal Structure, andin vitroAntitumor Activity of a Novel Tetranuclear Di-n-Butyltin(IV)." Координационная химия 39, no. 8 (2013): 463–67. http://dx.doi.org/10.7868/s0132344x13070025.

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21

Kayser, Francois, Monique Biesemans, Mohammed Boualam, et al. "A Novel 2:3 Condensation Complex of Salicylaldoxime and Di-n-butyltin(IV) Oxide." Organometallics 13, no. 4 (1994): 1098–113. http://dx.doi.org/10.1021/om00016a014.

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22

Hao-Long, Xu. "Synthesis and Crystal Structure of One Trinuclear di-n-butyltin(IV) Complex with Salicylaldoxime." Journal of Chemical Crystallography 39, no. 4 (2008): 299–302. http://dx.doi.org/10.1007/s10870-008-9476-x.

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23

Poli, G., C. J. Cheer, and W. H. Nelson. "The crystal and molecular structure of BIS(1,3-diphenylpropane-1,3-dionato)-Di-n-butyltin(IV)." Journal of Organometallic Chemistry 306, no. 3 (1986): 347–54. http://dx.doi.org/10.1016/s0022-328x(00)98996-4.

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24

Ma, Chunlin, Yinfeng Han, and Rufen Zhang. "Synthesis, characterizations and crystal structures of di-n-butyltin(IV) complexes with heteroatomic (N, O or S) acid." Journal of Organometallic Chemistry 689, no. 9 (2004): 1675–83. http://dx.doi.org/10.1016/j.jorganchem.2004.02.024.

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25

Gielen, Marcel, Muriel Mélotte, Ghanem Atassi, and Rudolph Willem. "Synthesis, characterization and antitumour activity of 7,7-di-n-butyl-5,9-dioxo-6,8-dioxa-7-stanna-spiro[3,5]nonane, a di-n-butyltin(IV) analog of “paraplatin”, and of a series of di-n-butyltin(IV) derivatives of mono- and disubstltuted malonic acids." Tetrahedron 45, no. 4 (1989): 1219–29. http://dx.doi.org/10.1016/0040-4020(89)80030-4.

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26

Yagi, Isao, Eiichiro Ikeda, and Yasuo Kuniya. "Pyrolytic properties of di-n-butyltin(IV) diacetate as a precursor for sprayed SnO2 thin films." Journal of Materials Research 9, no. 3 (1994): 663–68. http://dx.doi.org/10.1557/jmr.1994.0663.

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The saturated vapor pressure and pyrolytic properties of di-n-butyltin(IV) diacetate have been investigated with and without oxygen in order to understand the orientational growth of SnO2 thin films by spray pyrolysis. The dependence of the saturated vapor pressure on temperature was determined: log P(evap.)Torr = −2.827 × 103/T + 7.687. It has been found that the pyrolysis of this compound consisted of two stages: elimination of the n-butyl groups in a temperature range between about 280°and 310 °C, and of the acetoxy groups above 320 °C. Such decompositions were shifted toward lower temperat

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27

Liu, Chun-Ling, Dong-Sheng Zhu, and Chuan-Bi Li. "Synthesis, Structural Characterization, and Thermal Stability of Di-n-butyltin (IV) Carboxylate Containing a Sn2O2 Ring." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 46, no. 8 (2016): 1272–76. http://dx.doi.org/10.1080/15533174.2015.1004457.

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28

He, H. B., X. L. Ge, and B. F. Ruan. "Synthesis, crystal structure, and in vitro antitumor activity of a novel tetranuclear Di-n-butyltin(IV)." Russian Journal of Coordination Chemistry 39, no. 8 (2013): 560–64. http://dx.doi.org/10.1134/s1070328413070026.

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29

Gajda-Schrantz, K., L. Nagy, E. Kuzmann, and A. Vértes. "Coordination sphere symmetry of di-n-butyltin(IV) complexes containing ligands with {O,O} donor atoms." Journal of Radioanalytical and Nuclear Chemistry 232, no. 1-2 (1998): 151–58. http://dx.doi.org/10.1007/bf02383732.

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30

Gajda-Schrantz, Krisztina, László Nagy, Ernő Kuzmann, Attila Vértes, Jan Holeček, and Antonín Lyčka. "Symmetry of the co-ordination sphere of di-n-butyltin(IV) in complexes with sulfanylcarboxylic acids." Journal of the Chemical Society, Dalton Transactions, no. 12 (1997): 2201–6. http://dx.doi.org/10.1039/a608136c.

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31

Pokharia, Sandeep, Rachana Joshi, Mamta Pokharia, Swatantra Kumar Yadav, and Hirdyesh Mishra. "Electronic Structure Explanation for the Structure and Reactivity of di-n-Butyltin(IV) Derivative of Glycylphenylalanine." Proceedings of the National Academy of Sciences, India Section A: Physical Sciences 89, no. 2 (2019): 223–34. http://dx.doi.org/10.1007/s40010-018-0582-7.

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32

Mundus-Glowacki, Brigitte, Friedo Huber, Hans Preut, Giuseppe Ruisi, and Renato Barbieri. "Synthesis and spectroscopic characterization of dimethyl-, di-n-butyl-, di-t-butyl-and diphenyl-tin(iv) derivatives of dipeptides: Crystal and molecular structure of di-n-butyltin(iv) glycylvalinate." Applied Organometallic Chemistry 6, no. 1 (1992): 83–94. http://dx.doi.org/10.1002/aoc.590060111.

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33

Pokharia, Sandeep. "Theoretical insights on Organotin (IV)-protein interaction: Density Functional Theory (DFT) studies on di-n-butyltin(IV) derivative of Glycylvaline." Asian Journal of Research in Chemistry 8, no. 1 (2015): 7. http://dx.doi.org/10.5958/0974-4150.2015.00002.4.

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34

Švec, Petr, Aleš Eisner, Lenka Kolářová, Tomáš Weidlich, Vladimír Pejchal, and Aleš Růžička. "Use of C,N-chelated di-n-butyltin(IV) fluoride for the synthesis of acyl fluorides, fluoroformates and fluorophosgene." Tetrahedron Letters 49, no. 44 (2008): 6320–23. http://dx.doi.org/10.1016/j.tetlet.2008.08.060.

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35

Pokharia, Sandeep, Swatantra Kumar Yadav, and Hirdyesh Mishra. "An Atoms-in-Molecules Theory Interpretation for the Structure of Di-n-Butyltin(IV) Derivative of Glycylvaline." National Academy Science Letters 42, no. 4 (2019): 327–31. http://dx.doi.org/10.1007/s40009-018-0756-5.

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36

Wei, Chun-Ying, Pin Yang, Lian-Hong Wang, and Li Wang. "Synthesis, Characterization and in vitro Antitumour Activity of the Di-n-butyltin(IV) Complexes of Some Arylhydroxamates." Chinese Journal of Chemistry 20, no. 5 (2010): 453–61. http://dx.doi.org/10.1002/cjoc.20020200509.

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37

Tabassum, Sartaj, and Shipra Yadav. "Investigation of diorganotin(IV) complexes: Synthesis, characterization, in vitro DNA binding studies and cytotoxicity assessment of di-n-butyltin(IV) complex." Inorganica Chimica Acta 423 (November 2014): 204–14. http://dx.doi.org/10.1016/j.ica.2014.07.056.

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38

Ruisi, G., A. Silvestri, M. T. Lo Giudice, et al. "The antitumor activity of di-n-butyltin(IV) glycylglycinate, and the correlation with the structure of dialkyltin(IV) glycylglycinates in solution." Journal of Inorganic Biochemistry 25, no. 4 (1985): 229–45. http://dx.doi.org/10.1016/0162-0134(85)80023-4.

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39

Joshi, Anurag, Shashi Verma, R. B. Gaurb та R. R. Sharma. "Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation, Biological Evaluation, Structural Elucidation Based upon Spectral [IR, NMR (1H,13C,19F and119Sn)] Studies". Bioinorganic Chemistry and Applications 3, № 3-4 (2005): 201–15. http://dx.doi.org/10.1155/bca.2005.201.

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Stable, six coordinated Bu2SnLA type complexes have been prepared [where LH =RCOC:C(OH)N(C6H5)N:︹CCH3; R = -4-F-C6H4-(L1H), R = -4-Cl-C6H4-(L2H), R= -4-Br-C6H4-(L3H), R= -CF3(L4H) andAH=C(O)C6H4C(O)︹NCHR′COOH; R'= -H(A1H), -CH3(A2H), -CH(CH3)2(A3H)] by the interaction of 1:1:1 molar ratios of di-n-butyltin(IV) dichloride with corresponding organic moieties in refluxing benzene using two moles of Et3N as a base. In these complexes LH and AH behave as bidentate and coordination is taking place through oxygen, this is inferred from IR and13C NMR studies. These complexes possess tin atoms in skew

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40

Mohamad, Rapidah, Normah Awang, Nurul Farahana Kamaludin, Mukesh M. Jotani та Edward R. T. Tiekink. "Crystal structures and Hirshfeld surface analyses of bis[N,N-bis(2-methoxyethyl)dithiocarbamato-κ2S,S′]di-n-butyltin(IV) and [N-(2-methoxyethyl)-N-methyldithiocarbamato-κ2S,S′]triphenyltin(IV)". Acta Crystallographica Section E Crystallographic Communications 74, № 3 (2018): 302–8. http://dx.doi.org/10.1107/s2056989018001901.

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The crystal and molecular structures of the two title organotin dithiocarbamate compounds, [Sn(C4H9)2(C7H14NO2S2)2], (I), and [Sn(C6H5)3(C5H10NOS2)], (II), are described. Both structures feature asymmetrically bound dithiocarbamate ligands leading to a skew-trapezoidal bipyramidal geometry for the metal atom in (I) and a distorted tetrahedral geometry in (II). The complete molecule of (I) is generated by a crystallographic twofold axis (Sn site symmetry 2). In the crystal of (I), molecules self-assemble into a supramolecular array parallel to (10-1)viamethylene-C—H...O(methoxy) interactions. I

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41

Pokharia, Sandeep. "An Atoms-in-molecules (AIM) interpretation of organotin-peptide system: I. Di-n-butyltin(IV) derivative of glycyltryptophane." Asian Journal of Research in Chemistry 10, no. 2 (2017): 115. http://dx.doi.org/10.5958/0974-4150.2017.00017.7.

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42

Liu, Hong-Wen, Wen-Guan Lu, and Jia-Xun Tao. "Synthesis and Crystal Structure of Di-n-butyltin(IV) Complex with 2-Oxo-propionic Acid (4-Pyridinecarbonyl) Hydrazone." Chinese Journal of Chemistry 22, no. 1 (2010): 109–13. http://dx.doi.org/10.1002/cjoc.20040220123.

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43

García-Zarracino, Reyes, and Herbert Höpfl. "Structural characterization of dimethyl- and di-n-butyltin(IV) 2,3-pyridinedicarboxylate in solution and in the solid state." Applied Organometallic Chemistry 19, no. 4 (2005): 451–57. http://dx.doi.org/10.1002/aoc.773.

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44

Gielen, Marcel, Abdelaziz El Khloufi, Monique Biesemans, Bernard Mahieu, and Rudolph Willem. "Diethyl- and Di-n-Butyltin(IV) 3-Amino-4-Methylbenzoates: Synthesis, Spectroscopic Characterization and in Vitro Antitumor Activity." Bulletin des Sociétés Chimiques Belges 101, no. 3 (2010): 243–48. http://dx.doi.org/10.1002/bscb.19921010313.

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45

Diop, Tidiane, Adrienne Ndioléne, Mouhamadou Birame Diop, et al. "Synthesis, spectral (FT-IR, 1H, 13C) studies, and crystal structure of [(2,6-CO2)2C5H3NSnBu2(H2O)]2·CHCl3." Zeitschrift für Naturforschung B 76, no. 2 (2021): 127–32. http://dx.doi.org/10.1515/znb-2020-0195.

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Abstract Di-n-butyltin(IV) 2,6-pyridinedicarboxylate [(2,6-CO2)2C5H3NSnBu2(H2O)]2·CHCl3, has been synthesized and characterized by elemental analyses, infrared and NMR (1H and 13C) spectroscopy, and single-crystal X-ray diffraction. The title complex crystallizes in the triclinic space group P 1 ‾ $P&#x203e;{1}$ ; with a = 9.2330(4), b = 10.4790(5), c = 20.2489(8) Å, α = 89.439(4), β = 87.492(3), γ = 85.888(4)°, V = 1951.96(15) Å3, and Z = 2. In this complex, the 2,6-pyridinedicarboxylate groups are tetradentate, chelating, and bridging ligands for the tin(IV) atoms. NMR spectra showed tha

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46

Wen-Guan, Lu, Tao Jia-Xun, Li Xu-Yu та Wang Yu-Zhen. "Synthesis and Characterization of Bis-[oxo-bis(β-ferrocenyl trans-propenoic di-n-butyltin(IV))]". Acta Physico-Chimica Sinica 17, № 09 (2001): 836–39. http://dx.doi.org/10.3866/pku.whxb20010916.

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47

Meriem, Abdelkader, Rudolph Willem, Monique Biesemans, et al. "Synthesis, characterization andin vitro antitumour activity of di-n-butyltin(;iv) derivatives of some aromatic carboxylic acids, including aspirin." Applied Organometallic Chemistry 5, no. 3 (1991): 195–201. http://dx.doi.org/10.1002/aoc.590050309.

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48

Bou??lam, Mohammed, Monique Biesemans, Jacqueline Meunier-Piret, Rudolph Willem, and Marcel Gielen. "In vitro antitumour activities of a novel 2:3 condensation product of salicylaldoxime with di-n-butyltin(IV) oxide." Applied Organometallic Chemistry 6, no. 2 (1992): 197–205. http://dx.doi.org/10.1002/aoc.590060214.

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Salam, M. A., M. A. Affan, Fasihuddin B. Ahmad, et al. "Synthesis, spectral characterization and crystal structure of a novel trinuclear di-n-butyltin(IV) complex with pyruvic acid-N(4)-cyclohexylthiosemicarbazone (H2PACT)." Journal of Organometallic Chemistry 696, no. 26 (2012): 4202–6. http://dx.doi.org/10.1016/j.jorganchem.2011.09.013.

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Narula, Suraj P., Shashi K. Bharadwaj, Yash Sharda, David C. Povey та Gallienus W. Smith. "Molecular structure of 1,2;3,4,di-μ,-nitrobenzoato-OO'-1,3-bis(o, m-, or p-nitrobenzoato)-l,2,4;2,3,4-di-μ3-oxotetrakis [di-n-butyltin(IV)] compounds". Journal of Organometallic Chemistry 430, № 2 (1992): 167–73. http://dx.doi.org/10.1016/0022-328x(92)86004-n.

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