Relevant bibliographies by topics / Multinuclear organotin

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Academic literature on the topic 'Multinuclear organotin'

Author: Grafiati
Published: 18 May 2024
Last updated: 31 July 2025

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Journal articles on the topic "Multinuclear organotin"

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Cherryman, Julian C., and Robin K. Harris. "New Multinuclear Experiments on Solid Organotin Fluorides." Journal of Magnetic Resonance 128, no. 1 (1997): 21–29. http://dx.doi.org/10.1006/jmre.1997.1206.

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2

Rashid, Faisal, Noor Uddin, Saqib Ali, et al. "New triorganotin(iv) compounds with aromatic carboxylate ligands: synthesis and evaluation of the pro-apoptotic mechanism." RSC Advances 11, no. 8 (2021): 4499–514. http://dx.doi.org/10.1039/d0ra06695h.

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Three new organotin(iv) carboxylate compounds were synthesized and structurally characterized by elemental analysis and FT-IR and multinuclear NMR (<sup>1</sup>H, <sup>13</sup>C, <sup>119</sup>Sn) spectroscopy.
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Matela, Garima, and Robina Aman. "Organotin(IV) complexes of carboxylic acid derivatives." Open Chemistry 10, no. 1 (2012): 1–15. http://dx.doi.org/10.2478/s11532-011-0107-6.

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AbstractA comprehensive review, &gt;100 references, on organotin(IV) complexes of the carboxylic acid derivatives are presented with special reference to their methods of synthesis, spectroscopic and structural studies and their biological activities. The structures of these complexes are discussed on the basis of IR, multinuclear (1H-, 13C- and 119Sn-) NMR.
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4

Tagne Kuate, Alain C., Roger A. Lalancette, and F. Jäkle. "Planar-chiral ferrocenylphosphine-borane complexes featuring agostic-type B–H⋯E (E = Hg, Sn) interactions." Dalton Transactions 46, no. 19 (2017): 6253–64. http://dx.doi.org/10.1039/c6dt04791b.

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Ferrocenylphosphine-borane adducts with Lewis acidic organotin and organomercury substituents inortho-position show rare agostic-type B–H⋯E (E = Sn, Hg) interactions that have been studied by single crystal XRD, multinuclear solution NMR, and computational methods.
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Singh, Har Lal, and A. K. Varshney. "Synthetic, Structural, and Biochemical Studies of Organotin(IV) with Schiff Bases Having Nitrogen and Sulphur Donor Ligands." Bioinorganic Chemistry and Applications 2006 (2006): 1–7. http://dx.doi.org/10.1155/bca/2006/23245.

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Three bidentate Schiff bases having nitrogen and sulphur donor sequences were prepared by condensing S-benzyldithiocarbazate (NH2NHCS2CH2C6H5) with heterocyclic aldehydes. The reaction of diphenyltin dichloride with Schiff bases leads to the formation of a new series of organotin(IV) complexes. An attempt has been made to prove their structures on the basis of elemental analyses, conductance measurements, molecular weights determinations, UV, infrared, and multinuclear magnetic resonance (H1,C13, andS119n) spectral studies. Organotin(IV) complexes were five- and six-coordinate. Schiff bases an
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Nandu Bala Sharma and Yogesh Kumar Gupta. "A Review : Synthetic and Applied Aspects of Organotin(IV) Complexes of Schiff Bases." Journal of Advanced Chemical Sciences 10, no. 4 (2024): 816–21. https://doi.org/10.30799//jacs.263.24100403.

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The coordinating atoms of oxygen, nitrogen, sulfur, or phosphorus in Schiff bases with different coordination numbers create complexes with organotin(IV) moiety. The structure was usefully revealed by the development of novel spectroscopic techniques such as FT-IR, multinuclear (1H, 13C, 119Sn) NMR, and X-ray crystallography. A lot of research has been done recently on organotin(IV) complexes of Schiff base because of their antibacterial, antinematicidal, anti-inflammatory, antitumor, and antiurease properties. In order to understand the synthesis, spectroscopic characterization, biological si
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7

Shahid, Khadija, Saira Shahzadi, and Saqib Ali. "Synthesis, coordination and biological aspects of organotin(IV) derivatives of 4-[(2,4-dinitrophenyl)amino)]-4-oxo-2-butenoic acid and 2-{[(2,4-dinitrophenyl)amino]carbonyl}benzoic acid." Journal of the Serbian Chemical Society 74, no. 2 (2009): 141–54. http://dx.doi.org/10.2298/jsc0902141s.

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New series of organotin(IV) complexes of aniline derivatives, R2SnL2 and R3SnL [where R = Me, n-Bu, Ph, n-Oct] have been synthesized by the reaction of HL1 and HL2 with respective organotin halides or oxides. Experimental details for the preparation and characterization (including elemental analysis, IR and multinuclear NMR (1H-, 13C- and 119Sn-) spectra in CDCl3 and EI mass spectra of both series are provided. The binding sites of the ligands were identified by means of FTIR spectroscopic measurements. It was found that in all cases the organotin(IV) moiety reacts with the oxygen of COO- grou
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8

Raj, Kumar Dubey, and Pratap Singh Avadhesh. "Synthetic and applied aspects of tin(IV) and organotin(IV) complexes of various Schiff bases." Journal of Indian Chemical Society Vol. 92, Jul 2015 (2015): 1051–63. https://doi.org/10.5281/zenodo.5606763.

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Synthetic Inorganic and Metallo-organic Research Laboratory, Department of Chemistry, University of Allahabad, Allahabad-211 002, Uttar Pradesh, India <em>E-mail</em> : rajalkoxy@yahoo.com <em>Manuscript received online 14 October 2014, accepted 22 October 2014</em> The tin(IV) and organotin(IV) moiety form complexes with Schiff bases containing oxygen, nitrogen, sulphur or phosphorus coordinating atoms with varied coordination number. The development of new spectroscopic techniques FT-IR, multinuclear (<sup>1</sup>H-, <sup>13</sup>C-, <sup>119</sup>Sn-) NMR, X-ray crystallography provided use
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Sabiha Khanam, Sabiha Khanam, Khadija Shahid Khadija Shahid, Muhammad Sirajuddin Muhammad Sirajuddin, and Saqib Ali and Hameed Ullah Saqib Ali and Hameed Ullah. "Synthesis, Spectral Characterization and Biological Evaluation of Organotin(IV) Complexes of Aniline Derivatives of Naturally Occurring Betulinic Acid." Journal of the chemical society of pakistan 41, no. 4 (2019): 725. http://dx.doi.org/10.52568/000785/jcsp/41.04.2019.

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Betulinic acid (triterpene) has shown an immense potential towards the development of anticancer, antiviral, antimalarial, antifungal, antioxidant and antiprotozoal agents. Cis-platin (cytotoxic agent) has diverted attention of chemists towards organotin complexes with marked pharmacological activities. In present work aniline derivatives of Betulinic acid were synthesized followed by the synthesis of diorganotin and triorganotin metal complexes. These complexes were characterized by FT-IR and multinuclear NMR (1H and 13C) spectroscopy. The ligands and their organotin(IV) complexes were screen
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Said, Musa A., C. Hemavathi, S. Nagabrahmanandachari, K. C. Kumara Swamy, Damodara M. Poojary, and A. Clearfield. "Syntheses and structures of new mono and multinuclear organotin phosphinates." Proceedings / Indian Academy of Sciences 108, no. 3 (1996): 298. http://dx.doi.org/10.1007/bf02870065.

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Book chapters on the topic "Multinuclear organotin"

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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