Academic literature on the topic 'Organotin compounds' chemistry'

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Journal articles on the topic "Organotin compounds' chemistry"

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Rabiee, Navid, Moein Safarkhani, and Mostafa M. Amini. "Investigating the structural chemistry of organotin(IV) compounds: recent advances." Reviews in Inorganic Chemistry 39, no. 1 (2019): 13–45. http://dx.doi.org/10.1515/revic-2018-0014.

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AbstractOrganotin(IV) compounds have been considered for their outstanding industrial, medical and specific applications in the synthesis of various types of chemical compounds. In this review, we have focused on the structural chemistry of organotin(IV) compounds, including coordination chemistry, the effect of structure on reactions, bond formations from the perspective of structure and investigation of the structure of organotin(IV) compounds in different phases. The structural chemistry of organotin(IV) compounds is subject to interest due to their major impact on predicting the properties
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Sakai, Fumihiko, Hideaki Fujiwara, and Yoshio Sasaki. "The solution chemistry of organotin compounds." Journal of Organometallic Chemistry 310, no. 3 (1986): 293–301. http://dx.doi.org/10.1016/0022-328x(86)80193-0.

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Adeyemi, Jerry, and Damian Onwudiwe. "Organotin(IV) Dithiocarbamate Complexes: Chemistry and Biological Activity." Molecules 23, no. 10 (2018): 2571. http://dx.doi.org/10.3390/molecules23102571.

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Significant attention has been given to organotin(IV) dithiocabamate compounds in recent times. This is due to their ability to stabilize specific stereochemistry in their complexes, and their diverse application in agriculture, biology, catalysis and as single source precursors for tin sulfide nanoparticles. These complexes have good coordination chemistry, stability and diverse molecular structures which, thus, prompt their wide range of biological activities. Their unique stereo-electronic properties underline their relevance in the area of medicinal chemistry. Organotin(IV) dithiocabamate
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Allef, Petra, та Horst Kunz. "Stereoselective Synthesis of α-Arylalkylamines by Glycosylation-induced Asymmetric Addition of Organometallic Compounds to Imines". Zeitschrift für Naturforschung B 64, № 6 (2009): 646–52. http://dx.doi.org/10.1515/znb-2009-0609.

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Activation of imines of aromatic aldehydes by N-glycosylation with O-pivaloyl-galactopyranosyl bromide (pivalobromogalactose) and subsequent addition of organotin, organolithium, Grignard, or organozinc reagents afforded α-arylalkylamines with moderate to high diastereoselectivity.
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Siwacha, Priyanka, Surbhi Soni, Harish Kumar Sharmaa, and Manoj Kumara. "Synthesis, Characterization and Biological Studies of Some Organotin Compounds: (A-Review)." Oriental Journal Of Chemistry 36, no. 05 (2020): 871–78. http://dx.doi.org/10.13005/ojc/360511.

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Significant attention has been given to organotin (IV) amino acids compounds in recent years. Organometallic compounds are better known for their potentiality to stabilize peculiar stereochemistry of their complexes and application in agriculture, catalysis and as single source precursors. Due to the better stability and diverse molecular structures the complexes own a wide range of biological activities. These individual properties create an alliance of action in the hybrid complex. In this review, we discuss the chemistry of organotin (IV) complexes and their different aspects in various fie
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Eaborn, Colin. "Gmelin handbook of inorganic and organometallic chemistry. 8th Ed. Sn. organotin compounds. Part 19. Organotin-nitrogen compounds (concluded), Organotin-Phosphorus, -Arsenic, -Antimony, -Bismuth Compounds." Journal of Organometallic Chemistry 436, no. 2 (1992): C22. http://dx.doi.org/10.1016/0022-328x(92)85056-3.

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Meinema, Harry. "Organotin Compounds in Modern Technology." Organometallics 4, no. 9 (1985): 1696. http://dx.doi.org/10.1021/om00128a602.

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Pichler, Johann, Philipp Müller, Ana Torvisco, and Frank Uhlig. "Novel diaminopropyl substituted organotin compounds." Canadian Journal of Chemistry 96, no. 4 (2018): 411–18. http://dx.doi.org/10.1139/cjc-2017-0713.

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A novel synthetic pathway involving the desilylation of a tin trimethylsilyl species (Ph2Sn(SiMe3)2) towards nonprotected di(3-aminopropyl)tin dichloride ((H2N(CH2)3)2SnCl2) is described. Di(3-aminopropyl)tin dichloride is then converted to the respective dicarboxylates species (H2N(CH2)3)2Sn(OCOR)2 containing carboxylic acids of different lengths (R = –CH3, –(CH2)10CH3). Depending on the nature of R, discrete packing effects are observed in the solid state of di(3-aminopropyl)tin dicarboxylate derivatives. All the synthesized substances were characterized by 1H, 13C, and 119Sn nuclear magneti
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Buck, Bethany, Alessandro Mascioni, Lawrence Que, and Gianluigi Veglia. "Dealkylation of Organotin Compounds by Biological Dithiols: Toward the Chemistry of Organotin Toxicity." Journal of the American Chemical Society 125, no. 44 (2003): 13316–17. http://dx.doi.org/10.1021/ja0354723.

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Plasseraud, Laurent. "Organotin(IV) Complexes Containing Sn–O–Se Moieties: A Structural Inventory." Synthesis 50, no. 18 (2018): 3653–61. http://dx.doi.org/10.1055/s-0037-1610164.

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This review focuses on organotin compounds exhibiting Sn–O–Se moieties, the molecular structures of which have been previously resolved by single-crystal X-ray diffraction analysis. Three distinct classes of compounds have been identified. Thus, the various modes of coordination of selenite, selenate and organoseleninate anions with tin atoms of organotin(IV) fragments are illustrated and detailed.1 Introduction2 Organotin(IV) Selenite Complexes3 Organotin(IV) Selenate Complexes4 Organotin(IV) Organoseleninate Complexes5 Summary
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Dissertations / Theses on the topic "Organotin compounds' chemistry"

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Hill, Michael Stephen. "Organotin tetrazoles and related compounds." Thesis, University of Bath, 1994. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240694.

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O'Loughlin, Edward John. "Association of organotin compounds with aquatic humic substances /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487946776023338.

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Doidge-Harrison, Solange Maria Silva Veloso. "X-ray and spectroscopic studies of organotin compounds." Thesis, Robert Gordon University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304984.

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Ashby, J. R. "Formation and distribution of organotin compounds in the environment." Thesis, De Montfort University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.232890.

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Skerlj, Renato Tony. "Synthesis and chemistry of alkyl 2, 3-bis(trimethylstannyl)-2-alkenoates and related substances." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/29391.

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This thesis describes the synthesis and chemistry of alkyl 2,3-bis(trimethylstannyl)-2-alkenoates ((78) and (83)). It was shown that these compounds could be readily transformed into useful intermediates for the synthesis of functionalized, stereochemically defined tetrasub-stituted alkenes (87) and tricyclic dienes of general structure (322A). The synthesis and chemistry of compounds (277) and (278) is also described. The palladium(O)-catalyzed addition of hexamethylditin to a variety of α,β-acetylenic esters (90), afforded in a stereoselective manner, the corresponding alkyl (Z)-2,3-bis(tr
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Björn, Annika. "Microbial Transformation of Organotin Compounds under Simulated Landfill Conditions." Doctoral thesis, Linköpings universitet, Tema vatten i natur och samhälle, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-10278.

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Mono- and di-alkyltins are used extensively as heat stabilizers for processing of poly vinyl chloride (PVC). Tin mercaptide stabilizers are some of the most effective PVC stabilizers available. The main applications for tin stabilizers are building/construction products, such as pipes, fittings, siding and profiles (windows etc.), packaging and flexible PVC plastics. Most PVC products have been and are subjected to landfilling, when their use is terminated. The structure of the polymer itself and the substances used as additives have been a concern for environmental authorities in many countri
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Taylor, Oonah J. "A study of c-stannylated monosaccharide derivatives." Thesis, University of Aberdeen, 1988. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU602280.

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A series of C-stannylated monosaccharide derivatives were prepared and their chemistry studied. Derivatives having a hydroxyl group ? to tin, i.e. methyl 4,6-0- benzylidene-2(3)-deoxy-2(3)-triphenylstannyl-?-D-allopyranosides [(1) and (2)] and 6-deoxy-l,2-0-isopropylidene-6-triorganostannyl-?-D-glucofuranose (3, R=Me, 4, R=Ph) were prepared by reaction of appropriate triorgano-tin-lithiums with epoxy sugars. Reactions of 3 with TFA, acetyl chloride, benzoyl chloride, ethyl chloroformate, sulphur dioxide and TCNE produced via elimination, 5,-6- dideoxy-1,2-0-isopropylidene-?-D-xylo-hex-5-enofur
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Dunn, Kerri, and kerri dunn@deakin edu au. "Chiral organotin hydrides as enantioselective reducing agents." Deakin University. School of Nutrition and Public Health, 2000. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20061207.142326.

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This thesis reports on the feasibility of the utilization of organotin hydrides as enaantioselective free radical reducing agents. The chiral organotin hydrides prepared contain the bulky chiral (1R,2S,5R)-menthyl substituent and in some cases also contain a stereogenic tin centre. Reaction of (1R,2S,5R)-menthylmagnesium chloride (MenMgC1) with triphenyltin chloride in THF proceeds with epimerization of the C-1 carbon of the menthyl group and results in a mixture of (1R,2S,5R)-menthyltriphenyltin and (1S,2S.5R)-menthyltriphenyltin. Addition of Lewis bases such as triphenylphosphine to the T
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Bai, Haiping. "Solid-state NMR Studies of organotin compounds and of titania pigments." Thesis, Durham University, 1991. http://etheses.dur.ac.uk/6286/.

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Harston, P. "The thermal stability encapsulation in glass, and exchange reactions, of organotin compounds." Thesis, University of Aberdeen, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387462.

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The thermolysis of organotin compounds R<sub>3</sub>SnX (R=Ph, Bu, Cy, Neo, Bnz; X=Cl, OSnRa, SnR<sub>3</sub>, O<sub>2</sub>CR'), R<sub>2</sub>"SnO and R"Sn(O)OH (where R"=Bu, Oct) has been investigated by thermal analysis, gas chromatography and Mössbauer spectroscopy. Several decompositions of R<sub>3</sub>SnX occurred via disproportionation to the tetra- and di-organotin products. Organotin compounds were successfully encapsulated into sized metal acetate glasses, with little or no decomposition of the organotin. Both halide/acetate and oxide/acetate exchanges occurred in the melt; partial
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Books on the topic "Organotin compounds' chemistry"

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Davies, Alwyn George. Organotin chemistry. 2nd ed. VCH, 2004.

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Davies, Alwyn George. Organotin chemistry. 2nd ed. Wiley-VCH, 2004.

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Organotin chemistry. VCH, 1997.

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Organotin chemistry. Elsevier, 1989.

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International, Conference on the Organometallic and Coordination Chemistry of Germanium Tin and Lead (6th 1989 Brussels Belgium). Main group metal chemistry: Incorporating silicon, germanium, tin and lead compounds. Freund, 1989.

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I͡A︡, Lukevit͡s︡ Ė, Ignatovich L, Gelʹman I. V, and Organiskās sintēzes institūts (Latvijas Zinātn̦u akadēmija), eds. VII-th International Conference on the Organometallic and Coordination Chemistry of Germanium, Tin, and Lead, Riga Latvia, September 20-25, 1992: Abstracts. Institute of Organic Synthesis, Latvian Academy of Sciences, 1992.

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7

Blair, W. R. Characterization of long term controlled release dynamics and identification of butyltin species released from OMP impregnated wood pilings. U.S. Dept. of Commerce, National Bureau of Standards, 1987.

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Blair, W. R. Characterization of long term controlled release dynamics and identification of butyltin species released from OMP impregnated wood pilings. U.S. Dept. of Commerce, National Bureau of Standards, 1987.

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Rappoport, Zvi, and Ilan Marek, eds. The Chemistry of Organozinc Compounds. John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/9780470093399.

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Davies, Alwyn G. Organotin Chemistry. Wiley & Sons, Incorporated, John, 2006.

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Book chapters on the topic "Organotin compounds' chemistry"

1

Fugami, Keigo, and Masanori Kosugi. "Organotin Compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45313-x_4.

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Blunden, Stephen J., and Colin J. Evans. "Organotin Compounds." In The Handbook of Environmental Chemistry. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-540-46211-8_1.

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Sousa, Ana C. A., M. Ramiro Pastorinho, Shin Takahashi, and Shinsuke Tanabe. "Organotin Compounds from Snails to Humans." In Environmental Chemistry for a Sustainable World. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-02387-8_4.

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Jousseaume, Bernard, and Michel Pereyre. "The uses of organotin compounds in organic synthesis." In Chemistry of Tin. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4938-9_9.

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Miller, D. P., and P. J. Craig. "The analysis of organotin compounds from the natural environment." In Chemistry of Tin. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4938-9_15.

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Jambor, R., and L. Dostál. "Hypervalent organotin, aluminium, antimony and bismuth Y,C,Y-chelate complexes." In The Chemistry of Pincer Compounds. Elsevier, 2007. http://dx.doi.org/10.1016/b978-044453138-4/50017-9.

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Morabito, Roberto. "Sampling and sample treatment in the analysis of organotin compounds in environmental samples." In Comprehensive Analytical Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/s0166-526x(03)41030-1.

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