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Journal articles on the topic 'Organotin compounds' chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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7

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

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8

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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9

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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10

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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11

Saxena, Anil K. "Organotin compounds: Toxicology and biomedicinal applications." Applied Organometallic Chemistry 1, no. 1 (1987): 39–56. http://dx.doi.org/10.1002/aoc.590010107.

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12

Watta, Baerbel, Wilhelm P. Neumann, and Josef Sauer. "Organotin compounds. 31. Dodecamethylcyclohexastannane and dodecaperdeuteriomethylcyclohexastannane." Organometallics 4, no. 11 (1985): 1954–57. http://dx.doi.org/10.1021/om00130a006.

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13

Herber, Rolfe H., and Israel Nowik. "Metal Atom Dynamics of Organotin Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 6 (2011): 1336–40. http://dx.doi.org/10.1080/10426507.2010.543103.

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14

Baba, Ibrahim, Amirah Faizah Abdul Muthalib, Yang Farina Abdul Aziz, and Ng Seik Weng. "New Dithiocarbamate Compounds from Organotin(IV)." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 6 (2011): 1326–29. http://dx.doi.org/10.1080/10426507.2010.548841.

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15

Aue, Walter A., Bernard J. Flinn, Christopher G. Flinn, Veluppillai Paramasigamani, and Kathleen A. Russell. "Transformation and transmission of organotin compounds inside a gas chromatograph." Canadian Journal of Chemistry 67, no. 3 (1989): 402–10. http://dx.doi.org/10.1139/v89-063.

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A wide variety of mono-, di-, and tri-substituted tin compounds are transformed to, and transmitted as, chlorides, bromides, or iodides on injection into a gas chromatographic system doped with HCl, HBr, or HI, respectively. This transformation occurs directly from some thirty-odd analytes such as organotin oxides, hydroxides, organic esters, and other halides including fluorides. Three germanium compounds appear to behave similarly. A conventional, packed-column gas chromatographic set-up with flame photometric or flame ionization detector can tolerate the necessary acid doping. Compounds suc

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16

Wu, Yi-Bo, Bo-Wen Li, Fu-Xiang Li, Jian-Wei Xue, and Zhi-Ping Lv. "Synthesis and characteristics of organotin-based catalysts for acetylene hydrochlorination." Canadian Journal of Chemistry 96, no. 5 (2018): 447–52. http://dx.doi.org/10.1139/cjc-2017-0612.

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Organotin-based catalysts prepared by a facile and green synthesis route were used in the acetylene hydrochlorination reaction. In detail, organotin-based catalysts were directly synthesized by supporting both organotin and nitrogen compounds on a coal-based columnar activated carbon (AC) using both incipient wetness impregnation and calcination methods. Interestingly, upon addition of nitrogen compounds, the resultant (SnCl4 + C16H34Cl2Sn)/AC catalysts showed higher activity and stability when compared the its (SnCl4 + C16H34Cl2Sn + C2N4H4)/AC counterpart at 200 °C and a gas hourly space velo

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17

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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18

Yusof, Enis Nadia Md, Muhammad A. M. Latif, Mohamed I. M. Tahir, et al. "o-Vanillin Derived Schiff Bases and Their Organotin(IV) Compounds: Synthesis, Structural Characterisation, In-Silico Studies and Cytotoxicity." International Journal of Molecular Sciences 20, no. 4 (2019): 854. http://dx.doi.org/10.3390/ijms20040854.

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Six new organotin(IV) compounds of Schiff bases derived from S-R-dithiocarbazate [R = benzyl (B), 2- or 4-methylbenzyl (2M and 4M, respectively)] condensed with 2-hydroxy-3-methoxybenzaldehyde (oVa) were synthesised and characterised by elemental analysis, various spectroscopic techniques including infrared, UV-vis, multinuclear (1H, 13C, 119Sn) NMR and mass spectrometry, and single crystal X-ray diffraction. The organotin(IV) compounds were synthesised from the reaction of Ph2SnCl2 or Me2SnCl2 with the Schiff bases (S2MoVaH/S4MoVaH/SBoVaH) to form a total of six new organotin(IV) compounds th

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19

Lyčka, Antonín, Jaroslav Holeček, and Karel Handlíř. "119Sn, 13C and 1H NMR studies of aryloxy- and arylthio(1-butyl)stannanes." Collection of Czechoslovak Chemical Communications 54, no. 9 (1989): 2386–98. http://dx.doi.org/10.1135/cccc19892386.

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Two series of compounds have been prepared and studied by means of 119Sn, 13C, and 1H NMR spectroscopy, viz. aryloxy- and N-heteroaryloxytris(1-butyl)stannanes and their thio analogues Bu3SnER, and diaryloxy- and di(N-heteroaryloxy)bis(1-butyl)stannanes and their thio analogues Bu2Sn(ER)2, where E means oxygen or sulfur, Bu is 1-butyl, R = phenyl, 1-naphthyl, or 8-quinolyl. On the basis of mutual comparison of NMR spectral parameters of both series of organotin compounds and their comparison with NMR spectral parameters of analogous, purely organic compounds CH3ER it is possible to discuss the

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20

Luijten, J. G. A., and G. J. M. van der Kerk. "Investigations on organotin compounds. XXI: The preparation of organotin-substituted acetylenes by the decarboxylation of organotin acetylenecarboxylates." Recueil des Travaux Chimiques des Pays-Bas 83, no. 3 (2010): 295–300. http://dx.doi.org/10.1002/recl.19640830310.

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21

Teruel, José A., Antonio Ortiz, and Francisco J. Aranda. "Influence of organotin compounds on phosphatidylserine membranes." Applied Organometallic Chemistry 18, no. 3 (2004): 111–16. http://dx.doi.org/10.1002/aoc.592.

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22

Melník, Milan, Ján Garaj, Aladär Valent, and Mária Kohútová. "Isomers of Organotin Compounds II. Di - to Polymeric Compounds." Main Group Metal Chemistry 32, no. 1 (2009): 1–36. http://dx.doi.org/10.1515/mgmc.2009.32.1.1.

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23

Davies, A. G. "Gmelin handbook of inorganic chemistry. Sn—organotin compounds, part 17." Polyhedron 9, no. 17 (1990): 2191. http://dx.doi.org/10.1016/s0277-5387(00)84055-3.

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24

Buck-Koehntop, Bethany A., Fernando Porcelli, John L. Lewin, Christopher J. Cramer, and Gianluigi Veglia. "Biological chemistry of organotin compounds: Interactions and dealkylation by dithiols." Journal of Organometallic Chemistry 691, no. 8 (2006): 1748–55. http://dx.doi.org/10.1016/j.jorganchem.2005.12.047.

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25

Seyferth, Dietmar. "Gmelin Handbook of Inorganic Chemistry. Eighth Edition. Sn-Organotin Compounds." Organometallics 8, no. 2 (1989): 576. http://dx.doi.org/10.1021/om00104a606.

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26

Seyferth, Dietmar. "Gmelin Handbook of Inorganic Chemistry. Eighth Edition. Sn. Organotin Compounds." Organometallics 6, no. 9 (1987): 2020. http://dx.doi.org/10.1021/om00152a605.

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27

Laughlin, Roy B., W. French, H. Guard, R. B. Johannesen, and F. E. Brinckman. "Structure-activity relationships for organotin compounds." Environmental Toxicology and Chemistry 4, no. 3 (1985): 343–51. http://dx.doi.org/10.1002/etc.5620040309.

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28

Al-taweel, Samir A., and Hassan F. Al-saraierh. "SYNTHESIS OF THIOPHENE OLIGOMERS VIA ORGANOTIN COMPOUNDS." Phosphorus, Sulfur, and Silicon and the Related Elements 155, no. 1 (1999): 47–57. http://dx.doi.org/10.1080/10426509908044969.

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29

Hadi, Angham G., Khudheyer Jawad, Gamal A. El-Hiti, et al. "Photostabilization of Poly(vinyl chloride) by Organotin(IV) Compounds against Photodegradation." Molecules 24, no. 19 (2019): 3557. http://dx.doi.org/10.3390/molecules24193557.

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Poly(vinyl chloride) (PVC), a polymer widely used in common household and industrial materials, undergoes photodegradation upon ultraviolet irradiation, leading to undesirable physicochemical properties and a reduced lifetime. In this study, four telmisartan organotin(IV) compounds were tested as photostabilizers against photodegradation. PVC films (40-µm thickness) containing these compounds (0.5 wt%) were irradiated with ultraviolet light at room temperature for up to 300 h. Changes in various polymeric parameters, including the growth of hydroxyl, carbonyl, and alkene functional groups, wei

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30

Joshi, Ravi R., and Sudhir K. Gupta. "Ecotoxicity studies of some organotin compounds." Toxicological & Environmental Chemistry 34, no. 2-4 (1992): 133–38. http://dx.doi.org/10.1080/02772249209357786.

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31

TAKEUCHI, Masahiro, Kazuko MIZUISHI, and Toshiyuki HOBO. "Determination of Organotin Compounds in Environmental Samples." Analytical Sciences 16, no. 4 (2000): 349–59. http://dx.doi.org/10.2116/analsci.16.349.

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32

Shawky, S., H. Emons, and H. W. Dürbeck. "Speciation of organotin compounds in fish samples." Anal. Commun. 33, no. 3 (1996): 107–10. http://dx.doi.org/10.1039/ac9963300107.

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33

Mehring, Michael, Christian Löw, Markus Schürmann, and Klaus Jurkschat. "Intramolecular Donor-Assisted Cyclization of Organotin Compounds." European Journal of Inorganic Chemistry 1999, no. 5 (1999): 887–98. http://dx.doi.org/10.1002/(sici)1099-0682(199905)1999:5<887::aid-ejic887>3.0.co;2-2.

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34

Vighi, M., and D. Calamari. "QSARs for organotin compounds on Daphnia magna." Chemosphere 14, no. 11-12 (1985): 1925–32. http://dx.doi.org/10.1016/0045-6535(85)90134-1.

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35

de Vos, Dick, Rudolph Willem, Marcel Gielen, Kyra E. van Wingerden, and Kees Nooter. "The Development of Novel Organotin Anti-Tumor Drugs: Structure and Activity." Metal-Based Drugs 5, no. 4 (1998): 179–88. http://dx.doi.org/10.1155/mbd.1998.179.

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An overview of the development of anti-tumor organotin derivatives in selected classes of compounds is presented and discussed. High to very high in vitro activity has been found, sometimes equaling that of doxorubicin. Solubility in water is an important issue, dominating the in vivo testing of compounds with promising in vitro properties. The cytotoxicity of the compounds was increased by the presence of a bulky group, an active substituent or one or more polar substituents. Polar substituents may also improve the water solubility. Although organotin derivatives constitute a separate class o

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36

Kellner, G. L., and L. R. Sherman. "The Gender Toxicity of Select Organotin Compounds." Microchemical Journal 47, no. 1-2 (1993): 67–71. http://dx.doi.org/10.1006/mchj.1993.1013.

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37

Morabito, R. "Speciation of Organotin Compounds in Environmental Matrices." Microchemical Journal 51, no. 1-2 (1995): 198–206. http://dx.doi.org/10.1006/mchj.1995.1026.

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38

Yun-Feng, Zhao, Zhao Kong-Xiang, and Wu Yong-Ning. "Determination of Organotins in Aquatic Food by Gas Chromatography with Pulsed Flame Photometric Detection." Journal of AOAC INTERNATIONAL 91, no. 3 (2008): 653–59. http://dx.doi.org/10.1093/jaoac/91.3.653.

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Abstract A method based on gas chromatography (GC)-pulsed flame photometric detection (PFPD) was developed to determine the levels of organotins in aquatic food. After being purified by gel-permeation chromatography in ethyl actatetetrahydrofuran, the organotin compounds were derivatized by pentylmagnesium bromide. The derivative products were injected into the GC system and detected by PFPD (sulfur mode). The method was validated by analysis of the certified reference material and spiked samples. Recoveries of organotins ranged from 84.1 to 116.6 with relative standard deviation between 1.3 a

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39

Eng, G., D. Whalen, Y. Z. Zhang, et al. "Fungicidal Activity of Some Organotin Compounds againstCeratocystis ulmi." Applied Organometallic Chemistry 10, no. 7 (1996): 501–3. http://dx.doi.org/10.1002/(sici)1099-0739(199609)10:7<501::aid-aoc505>3.0.co;2-d.

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40

Duffy, John A., Paul Harston, James L. Wardell, and Peter J. Smith. "Encapsulation of organotin compounds in metal acetate glasses." Applied Organometallic Chemistry 4, no. 1 (1990): 69–71. http://dx.doi.org/10.1002/aoc.590040112.

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41

Lawson, G., and N. Ostah. "Speciation of organotin compounds by tandem mass spectrometry." Applied Organometallic Chemistry 7, no. 3 (1993): 183–91. http://dx.doi.org/10.1002/aoc.590070305.

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42

Gabbianelli, R., G. Falcioni, and G. Lupidi. "Effect of organotin compounds on trout AMP-deaminases." Applied Organometallic Chemistry 16, no. 1 (2001): 3–8. http://dx.doi.org/10.1002/aoc.250.

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43

Frigo, Dario M. "Gmelin Handbook of Inorganic Chemistry—8th edn. Organotin Compounds, Part 16." Polyhedron 9, no. 6 (1990): 897. http://dx.doi.org/10.1016/s0277-5387(00)81358-3.

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44

Ohta, Akihiro, Tokuhiro Watanabe, Kazuhiro Hayashi, et al. "Alkylation and Arylation of Pyrazines by Organotin Compounds." HETEROCYCLES 29, no. 1 (1989): 123. http://dx.doi.org/10.3987/com-88-4728.

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45

Lechner, Marie-Luise, Roland Fischer, and Frank Uhlig. "New Organotin Compounds Including a Tin–Zinc Bond." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 6 (2011): 1341–45. http://dx.doi.org/10.1080/10426507.2010.543101.

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46

Kamal, Marwan R., Samir A. Al-taweel, Mustafa M. El-abadelah та Khalid M. Abu Ajaj. "SYNTHESIS OF α-THIOPHENE OLIGOMERS VIA ORGANOTIN COMPOUNDS". Phosphorus, Sulfur, and Silicon and the Related Elements 126, № 1 (1997): 65–74. http://dx.doi.org/10.1080/10426509708043546.

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47

Hoch, M. "Organotin compounds in the environment — an overview." Applied Geochemistry 16, no. 7-8 (2001): 719–43. http://dx.doi.org/10.1016/s0883-2927(00)00067-6.

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48

Kabiersch, Grit, Johanna Rajasärkkä, Marja Tuomela, Annele Hatakka, Marko Virta, and Kari Steffen. "Bioluminescent Yeast Assay for Detection of Organotin Compounds." Analytical Chemistry 85, no. 12 (2013): 5740–45. http://dx.doi.org/10.1021/ac4003062.

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49

Dornsiepen, Eike, and Stefanie Dehnen. "Behavior of Organotin Sulfide Clusters towards Zinc Compounds." European Journal of Inorganic Chemistry 2019, no. 39-40 (2019): 4306–12. http://dx.doi.org/10.1002/ejic.201900508.

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50

Rojas‐León, Irán, Hazem Alnasr, Klaus Jurkschat, María G. Vasquez‐Ríos, Irán F. Hernández‐Ahuactzi, and Herbert Höpfl. "Molecular Tectonics with Di‐ and Trinuclear Organotin Compounds." Chemistry – A European Journal 24, no. 18 (2018): 4547–51. http://dx.doi.org/10.1002/chem.201800791.

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