Relevant bibliographies by topics / Diorganotin

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Diorganotin'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Diorganotin"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Diorganotin"

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Hall, Veronica J. "Structural systematics of diorganotin compounds /." Title page, contents and abstract only, 1998. http://web4.library.adelaide.edu.au/theses/09PH/09phh179.pdf.

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Hussain, Firasat [Verfasser]. "Hybrid organic-inorganic polyoxometalates functionalized by diorganotin groups / Firasat Hussain." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2008. http://d-nb.info/1034891162/34.

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Piedra-Garza, Luis Fernando [Verfasser]. "Hybrid organic-inorganic polyoxotungstates functionalized by diorganotin and -antimony linkers / Luis Fernando Piedra-Garza." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2009. http://d-nb.info/1034995715/34.

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Singla, Nisha. "Synthesis and characterization of diorganotin(IV) coordination polymers derived from silaalkylphosphonate and sulfonate based ligands." Thesis, IIT Delhi, 2016. http://localhost:8080/iit/handle/2074/7092.

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Perrone, Sylvie. "Copper(I)-mediated anti-SN2' allylic substitution reactions with diorganozinc reagents." Diss., [S.l.] : [s.n.], 2006. http://edoc.ub.uni-muenchen.de/archive/00006218.

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Fontes, i. Ustrell Montserrat. "Síntesi altament enantioselectiva d'alcohols propargílics i de diarilcarbinols per addició catalítica de diorganozinc a aldehids." Doctoral thesis, Universitat de Barcelona, 2003. http://hdl.handle.net/10803/2786.

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Al llarg d'aquesta tesi es presenten diferents metodologies originals basades en l'addició enantioselectiva de diorganozincs sobre aldehids catalitzada per &#946;-aminoalcohols, desenvolupats amb anterioritat en el nostre grup de recerca. S'obtenen d'aquesta manera alcohols quirals, que són substàncies d'alt interès sintètic, amb elevades enantioselectivitats i molt bons rendiments químics.<br/><br/>En concret, s'aconsegueix el desenvolupament d'un mètode altament eficaç per a l'addició de Et[sub2]Zn a aldehids propargílics mitjançant la transformació del triple enllaç en el corresponent compl
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Campbell, Matthew James Johnson Jeffrey Scott. "I. Mechanistic studies of a copper-catalyzed electrophilic amination of diorganozinc reagents reagents by O-benzoyl N,N-dialkylhydroxylamines II. Development of a 3-Exo-Dig cyclization for the preparation of vinylidene cyclopropanes III. Total synthesis of +-polyanthellin A." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2009. http://dc.lib.unc.edu/u?/etd,2881.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2010.<br>Title from electronic title page (viewed Jun. 23, 2010). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
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Hall, Veronica J. (Veronica Jane). "Structural systematics of diorganotin compounds / Veronica J. Hall." 1998. http://hdl.handle.net/2440/19288.

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Addendum inserted.<br>Includes bibliographical references.<br>x, 189 p. : ill. ; 30 cm.<br>Title page, contents and abstract only. The complete thesis in print form is available from the University Library.<br>This combined crystallographic and theoretical study of selected organotin systems has addressed the question whether crystal packing effects can significantly influence molecular geometry. Attempts at correlating changes in Sn-ligand parameters with the Lewis Acidity of the tin centre and/or the Lewis basicity of the ligand were also undertaken in this study.<br>Thesis (Ph.D.)--Universi
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Hussain, Firasat. "Hybrid organic-inorganic polyoxometalates functionalized by diorganotin groups /." 2006. http://www.jacobs-university.de/phd/files/1149094690.pdf.

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Piedra-Garza, Luis Fernando. "Hybrid organic-inorganic polyoxotungstates functionalized by diorganotin and -antimony linkers /." 2009. http://www.jacobs-university.de/phd/files/1252503406.pdf.

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Books on the topic "Diorganotin"

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Wissing, Elmo. Group-transfer reactions of diorganozinc and triorganoaluminium reagents with 1,4-diaza-1,3-butadienes ...: Proefschrift ter verkrijging van de graad van doctor ... 1992. [Rijksuniversiteit te Utrecht?], 1993.

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Book chapters on the topic "Diorganotin"

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Jousseaume, B. "Diorganotin Oxides with Diorganotin Compounds." In Compounds of Group 14 (Ge, Sn, Pb). Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00307.

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Ang, Tian Tse, and Lian Ee Khoo. "Synthesis and characterization of a series of diorganotin derivatives of ex-amino acids." In Chemistry and Technology of Silicon and Tin. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198555803.003.0046.

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Abstract Recently several diorganotin compounds of bicyclic structure have been found to be active in vivo against P388 lymphocytic leukaemia in mice. This has prompted us to prepare and characterize eight new diorganotin derivatives of comparable structural similarity to the above-mentioned compounds by condensing diorganotin oxides, R SnO, with the Schiff base of the following a-amino acids, (1)-(4).
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Gauron, V., B. Jousseaume, M. Pereyre J. B. Verlhac,, and J. M. Frances. "How silicon and tin meet in polymer and organic synthesis." In Chemistry and Technology of Silicon and Tin. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198555803.003.0017.

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Abstract The organic chemistry of silicon and tin has gained much significance in recent years on both academic and industrial grounds. At Bordeaux, we have been involved in research where both silicon and tin have featured synergistically. Two examples are presented in this paper. The first topic deals with polymer science and describes the preparation and the applications of new latent organotin catalysts for the reticulation of polyorganosiloxane chains (SiOH/SiOR and SiOH/SiH polycondensations). The underlying principle is to use bis(2-acyloxyalkyl)diorganotins, which are themselves not ca
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Gielen, M., A. Meriem, M. Boualam, A. Delmotte, R. Willem,, and D. de Vos. "Tin-based antitumour drugs: past, present, and future." In Chemistry and Technology of Silicon and Tin. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198555803.003.0022.

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Abstract The screening results obtained on the antitumour activity of several series of diorganotin compounds against L1210, P388, and P815 cancer cells in mice are reviewed, and perspectives for future research in this area delineated.
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Wood, M. E. "Using Diorganotin Dihalides and Tin(IV) Halides." In Compounds of Group 14 (Ge, Sn, Pb). Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00279.

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Wood, M. E. "Disproportionation Between Polymeric "Diorganostannane" Reagents and Diorganotin Dihalides." In Compounds of Group 14 (Ge, Sn, Pb). Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00289.

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Knochel, P. "Bis(α-halomethyl)zincs or Other Zinc Carbenoids from a Dihalomethane and a Diorganozinc." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au). Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-003-00122.

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Kozikowski, Alan P., and Michael N. Greco. "Synthesis of the Indole Alkaloid α-Cyclopiazonic Acid (αCA) by Two Sulfur-Mediated Reactions: Discovery of a Useful Diorganozinc Reaction." In Strategies and Tactics in Organic Synthesis. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-092429-8.50013-1.

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Conference papers on the topic "Diorganotin"

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Hussien, Nasry Jassim, Yang Farina, and Mohamad Jaber Al-Jeboori. "Synthesis and characterisation of diorganotin(IV) complexes of 3,4-dihydroxybenzaldehyde semicarbazone." In THE 2016 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2016 Postgraduate Colloquium. Author(s), 2016. http://dx.doi.org/10.1063/1.4966744.

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Costantino, Andrea, Gabriela Montiel Schneider, Romina Ocampo, Sandra Mandolesi, and Liliana Koll. "Mono- and diorganotin derivatives of (S)-BINOL diesters as precursors of C2 symmetry chiral catalysts." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a020.

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