Relevant bibliographies by topics / Organo-antimony Compounds

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  2. Book chapters

Academic literature on the topic 'Organo-antimony Compounds'

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

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Journal articles on the topic "Organo-antimony Compounds"

1

Yadav, Ram Nath Prasad. "Antimony(V) as Acceptors." Academic Voices: A Multidisciplinary Journal 5 (September 30, 2016): 34–39. http://dx.doi.org/10.3126/av.v5i0.15850.

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Lewis acidity of antimony(V) pentahalides and their organo substituted derivatives is well known. SbX5 acts as a strong acceptor towards halide ion as compared to antimony trihalide due to presence of two more electronegative halogen atoms in antimony pentahalide makes it better acceptor. Hexacoordinated organoantimony(V) complexes including chelating ligands are also known and hexacoordination and heptacoordination environment have been suggested for such compounds. The substitution of hydrocarbon groups bound to antimony by trifluoromethyl or pentafluorophenyl groups enhances the Lewis acidi
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LIEBMAN, J. F., J. A. M. SMOES, and S. W. SLAYDEN. "ChemInform Abstract: Thermochemistry of Organo-Arsenic, Antimony and Bismuth Compounds." ChemInform 26, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199501295.

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Yang, Hui-e., Heng-dao Quan, Masanori Tamura, and Akira Sekiya. "Investigation into antimony pentafluoride-based catalyst in preparing organo-fluorine compounds." Journal of Molecular Catalysis A: Chemical 233, no. 1-2 (2005): 99–104. http://dx.doi.org/10.1016/j.molcata.2004.12.040.

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Garje, Shivram S., and Vimal K. Jain. "ChemInform Abstract: The Chemistry of Organo-Arsenic, -Antimony, and -Bismuth Compounds: An Overview." ChemInform 30, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199926305.

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Li, Long, Yihao Zhang, Ying Li, et al. "Polymeric Membrane Fluoride-Selective Electrodes Using Lewis Acidic Organo-Antimony(V) Compounds as Ionophores." ACS Sensors 5, no. 11 (2020): 3465–73. http://dx.doi.org/10.1021/acssensors.0c01481.

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Matsuda, Haruo, Akira Ninagawa, and Hiroshi Hasegawa. "Reaction of Carbon Dioxide with 1-Phenylaziridine Catalyzed by Organo-antimony and -tin Compounds." Bulletin of the Chemical Society of Japan 58, no. 9 (1985): 2717–18. http://dx.doi.org/10.1246/bcsj.58.2717.

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Akhtar, Muhammad Shoaib, Zulfiqar Khan, Muhammad Naveed Mushtaq, and Muhammad Salman Akhtar. "Comparative Evaluation of Analgesic, Anti-inflammatory and Antipyretic Effects of Synthetic Derivatives of Organoantimony (?) Ferocenyl Benzoate with Piroxicam." Bangladesh Pharmaceutical Journal 19, no. 1 (2016): 15–24. http://dx.doi.org/10.3329/bpj.v19i1.29230.

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The current study was planned to evaluate comparative anti-inflammatory, analgesic and anti-pyretic activities of two newly synthesized organo-antimony (v) ferrocenyl benzoate derivatives with piroxicam. Anti-microbial activity of these compounds was also screened against two microorganisms. Analgesic effect of test compounds was evaluated by formalin-induced paw licking test in mice. The test compounds at 50 and 100 mg/kg b.w. doses exhibited significant (p<0.001) reduction of paw licking in treated mice comparable with standard drug piroxicam. Anti-inflammatory activity was assessed again
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Saito, Norimichi, Hiroshi Nishihara, and Kunitsugu Aramaki. "The mechanism for corrosion protective film formation on iron and nickel in acid solutions with organo-antimony compounds." Corrosion Science 33, no. 8 (1992): 1253–65. http://dx.doi.org/10.1016/0010-938x(92)90134-o.

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9

Nag, Ekta, Aditya Kulkarni, Sai Manoj N. V. T. Gorantla, et al. "Fluorescent organo-antimony compounds as precursors for syntheses of redox-active trimeric and dimeric alkali metal antimonides: an insight into electron transfer reduction processes." Dalton Transactions 51, no. 5 (2022): 1791–805. http://dx.doi.org/10.1039/d1dt03398k.

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Fluorescent diarylchlorostibane, distibane are utilized as precursors for syntheses of redox-active dimeric/trimeric alkali-metal antimonides by reductive dehalogenation. DFT and EDA-NOCV analysis are performed to shed light on the electron transfer mechanism.
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Gibbons, Martin N., Alexander J. Blake, and D. Bryan Sowerby. "Oxygen bridged hexa(organo)di-antimony compounds: Hydrolysis by traces of moisture and crystal structures of [SbR3Br]2O, where R = p- or o-tolyl." Journal of Organometallic Chemistry 543, no. 1-2 (1997): 217–25. http://dx.doi.org/10.1016/s0022-328x(97)00208-8.

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Book chapters on the topic "Organo-antimony Compounds"

1

"12. Introduction of Fluorine Using Antimony and Vanadium Fluorides : 12.3. Introduction of Fluorine with Organo-Substituted Antimony Fluorides (PhnSbF5 −n,n = 1–3)." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111163.

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2

"Phosphorus, Antimony, and Bismuth Compounds." In Organo Main Group Chemistry. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118025918.ch6.

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"12. Introduction of Fluorine Using Antimony and Vanadium Fluorides : 12.1. Replacement of Halogens by Fluorine with Antimony(III) Fluoride." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111161.

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"12. Introduction of Fluorine Using Antimony and Vanadium Fluorides." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111160.

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"12. Introduction of Fluorine Using Antimony and Vanadium Fluorides : 12.2. Replacement of Halogens by Fluorine and Addition of Fluorine to C = C Bonds with Antimony(V) Fluoride and Fluoroantimonates." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111162.

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"12. Introduction of Fluorine Using Antimony and Vanadium Fluorides : 12.4. Introduction of Fluorine with Vanadium(V) Fluoride." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111164.

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