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Relevant bibliographies by topics / Organotin Phenols

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Academic literature on the topic 'Organotin Phenols'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Organotin Phenols"

1

Fidelibus, Pablo M., Gustavo F. Silbestri, María T. Lockhart, Sandra D. Mandolesi, Alicia B. Chopa, and Julio C. Podestá. "Three-step synthesis of arylpolyboronic acids from phenols via organotin compounds." Applied Organometallic Chemistry 21, no. 8 (2007): 682–87. http://dx.doi.org/10.1002/aoc.1225.

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Etaiw, Safaa El-din H., and Amal H. Werida. "Three-dimensional organotin-hexacyanoferrate polymers as effective oxidizing reagents towards phenols." Applied Organometallic Chemistry 24, no. 11 (2010): 805–8. http://dx.doi.org/10.1002/aoc.1706.

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3

Wezel, Annemarie P. "Chemical and biological aspects of ecotoxicological risk assessment of ionizable and neutral organic compounds in fresh and marine waters: a review." Environmental Reviews 6, no. 2 (1998): 123–37. http://dx.doi.org/10.1139/a98-007.

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The effects of salinity and pH on the partitioning behaviour and toxicity of ionizable and neutral organics and organotin compounds in aquatic ecosystems are reviewed. The pH and pKa are of importance for the distribution over n-octanol and water (Dow) of ionizable compounds. Dow increases with salinity for ionized organics up to 3 times and for organotins up to 1000 times. Neutral acids partition more strongly to the phospholipids than their ions; however, differences are smaller than for Dow. For dissociated phenols, the distribution over the membrane and water (Dmw) depends on counterion co

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4

Su, Kun Mei, Zhen Huan Li, Ming Ding, and Xiao Long He. "The Synthesis of Diphenyl Carbonate from Dimethyl Carbonate and Phenol over Modified Organotin Catalysts." Advanced Materials Research 233-235 (May 2011): 124–27. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.124.

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Organotin catalysts were modified with sodium molybdate, sodium tungstate and sodium vanadate, and the modified organotin catalysts displayed high activity in transesterification of dimethyl carbonate (DMC) with phenol into diphenyl carbonate (DPC).

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5

Nikitin, E. A., D. B. Shpakovsky, V. Yu Tyurin, et al. "Novel organotin complexes with phenol and imidazole moieties for optimized antitumor properties." Journal of Organometallic Chemistry 959 (February 2022): 122212. http://dx.doi.org/10.1016/j.jorganchem.2021.122212.

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6

Dodokhova, Margarita Avdeevna, Inga Movlievna Kotieva, Andrej Vladimirovich Safronenko, et al. "Organotin compounds as effective antimetastatic substances in the treatment of epidermoid lung carcinoma Lewis (LLC) in an experiment." Journal of Clinical Oncology 39, no. 15_suppl (2021): e15054-e15054. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e15054.

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e15054 Background: Lung cancer occupies one of the first places in the structure of oncological diseases in the world. Reducing the life expectancy of patients, as a rule, occurs as a result of metastatic complications, so the search for new antimetastatic agents is an urgent task for experimental pharmacology and oncology. The aim of our study is to assess the severity of metastatic lesion in the Lewis lung epidermoid carcinoma (LLC) model in the presence of an organotin compound. Methods: The study was conducted on experimental C57BL/6 mice (n = 24, each group contained 12 mice) with LLC (su

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7

Smolyaninov, Ivan V., Andrey I. Poddel’sky, Daria A. Burmistrova, et al. "The Synthesis and Biological Activity of Organotin Complexes with Thio-Schiff Bases Bearing Phenol Fragments." International Journal of Molecular Sciences 24, no. 9 (2023): 8319. http://dx.doi.org/10.3390/ijms24098319.

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A number of novel di- and triorganotin(IV) complexes 1–5 (Ph2SnL1, Ph2SnL2, Et2SnL2, Ph3SnL3, Ph3SnL4) with mono- or dianionic forms of thio-Schiff bases containing antioxidant sterically hindered phenol or catechol fragments were synthesized. Compounds 1–5 were characterized by 1H, 13C NMR, IR spectroscopy, and elemental analysis. The molecular structures of complexes 1 and 2 in the crystal state were established by single-crystal X-ray analysis. The antioxidant activity of new complexes as radical scavengers was estimated in DPPH and ABTS assays. It was found that compounds 4 and 5 with free

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8

BUCHALLA, RAINER, CHRISTIAN SCHÜTTLER, and KLAUS WERNER BÖGL. "Effects of Ionizing Radiation on Plastic Food Packaging Materials: A Review." Journal of Food Protection 56, no. 11 (1993): 998–1005. http://dx.doi.org/10.4315/0362-028x-56.11.998.

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Increased “global” migration into food simulants has been described as a consequence of irradiation, particularly with fatty media; development of off-odors and taint transfer into food simulants have been observed with various plastics. Additives, especially antioxidants, are destroyed during irradiation, and increased “specific” migration values have been observed under certain circumstances. Organotin stabilizers in PVC are ultimately degraded to SnCl4, and increased migration of tin compounds was observed after gamma irradiation. Degradation products of phenol antioxidants, that were also

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9

Zhang, Yuanzhuo, Songlin Wang, Zhongliang Xiao, Tong Chen, and Gongying Wang. "Mesoporous silica-anchored organotin as heterogeneous catalyst for the transesterification of dimethyl carbonate with phenol." Research on Chemical Intermediates 42, no. 9 (2016): 7213–22. http://dx.doi.org/10.1007/s11164-016-2530-y.

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10

Pettinari, Claudio, Fabio Marchetti, Riccardo Pettinari, Domenico Martini, Andrei Drozdov, and Sergei Troyanov. "Synthesis and characterisation of tin(IV) and organotin(IV) derivatives 2-{[(2-hydroxyphenyl)imino]methyl}phenol." Inorganica Chimica Acta 325, no. 1-2 (2001): 103–14. http://dx.doi.org/10.1016/s0020-1693(01)00654-5.

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Dissertations / Theses on the topic "Organotin Phenols"

1

Chatterjee, Debesh Kumar. "Arylazo phenoxy derivatives of organotin compounds." Thesis, University of North Bengal, 1990. http://hdl.handle.net/123456789/757.

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2

Lawrence, Monique A. M. "The adsorption of phenolic and organotin compounds by clays and cation exchanged clays." Thesis, Aston University, 1996. http://publications.aston.ac.uk/9677/.

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Quaternary ammonium exchanged laponites (Quat-laponites) show selectivity in the adsorption of phenols and chlorinated phenols. Strong adsorbate-adsorbent interactions are indicated by adsorption isotherms. Adsorption of phenols and chlorinated phenols by Quat-smectites is greater than that by the Bi Quat-Smectites prepared in this study. It is thought that the quaternary ammonium exchanged smectite components of the Bi Quat-smectites interact with each other (adsorbent-adsorbent interactions) reducing the number of sites available for adsorbate-adsorbent interactions. Solidification/stabilisa

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3

Yi, Xianliang Andy, and 易先亮. "A comprehensive study on the ecological toxicity and risk of triphenyltin to aquatic organisms." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/202351.

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Books on the topic "Organotin Phenols"

1

Lawrence, Monique Ann Marie. The adsorption of phenolic and organotin compounds by clays and cation exchanged clays. Aston University. Department of Chemical Engineering and Applied Chemistry, 1996.

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2

J, Sekizawa, World Health Organization, International Program on Chemical Safety., and Inter-Organization Programme for the Sound Management of Chemicals., eds. Triphenyltin compounds. World Health Organization, 1999.

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Book chapters on the topic "Organotin Phenols"

1

Rafii, Esfandiar, Jean Claude Maire*, Martin Ngassoum, Robert Faure,, and Louis Lena. "Application of organotin groups as markers in analysis of coal liquefaction products and petroleum fractions." In Chemistry and Technology of Silicon and Tin. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198555803.003.0002.

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Abstract Aside from their industrial applications, organotin compounds have also been widely used as intermediates or reagents in organic synthesis. More recently, organotin groups have been used as markers for the structural elucidation of complex molecules with the aid of spectroscopic techniques. The possibility of using tri-n-butyltin compounds as markers is illustrated, with reference to multinuclear NMR spectroscopy, for the quantitative analysis of phenols in liquid fractions derived from coal, and of sulphur compounds in petroleum fractions.

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2

Taber, Douglass F. "Substituted Benzenes: The Piers/Lau Synthesis of Hamigeran B." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0064.

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Govindasamy Sekar of the Indian Institute of Technology, Madras, developed ( Chem. Commun. 2011, 47, 5076) an environmentally friendly procedure for the amination of 1 to 2. Jens-Uwe Peters of Hoffmann-La Roche, Basel, showed (Tetrahedron Lett. 2011, 52, 749) that the Udenfriend protocol could be used to convert drugs such as 3 to their hydroxylated metabolites. Suman L. Jain and Anil K. Sinha of the Indian Institute of Petroleum reported (Chem. Commun. 2011, 47, 1610) complementary conditions for arene hydroxylation. Dimethyl aniline has been used, inter alia, as a nucleophile in enantioselec

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