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Relevant bibliographies by topics / Diorganotin dichloride

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Journal articles

Academic literature on the topic 'Diorganotin dichloride'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Diorganotin dichloride"

1

Deep, Gagan, Deepali Chaturvedi, and A. K. Narula. "Guanylurea derivatives of diorganotin(IV) dichloride." Journal of Coordination Chemistry 62, no. 12 (2009): 2058–66. http://dx.doi.org/10.1080/00958970902756044.

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2

Al-Allafb, Talal A. K., and Amer Abdul-Rahman. "Diorganotin (IV) Dichloride Complexes of some N-Arylfurfuralnitrones." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 27, no. 7 (1997): 985–96. http://dx.doi.org/10.1080/00945719708000241.

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3

Ma, Chunlin, Junhong Zhang, and Rufen Zhang. "Syntheses, characterization, and X-ray crystal structures of diorganotin(IV) derivatives of 2-pyridinethiolato-N-oxide." Canadian Journal of Chemistry 81, no. 10 (2003): 1070–75. http://dx.doi.org/10.1139/v03-134.

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The diorganotin(IV) dichloride reacts with sodium 2-pyridinethiolato-N-oxide in a 1:1 ratio to produce [Me2SnCl(2-SpyO)] (1), [Et2SnCl(2-SpyO)] (2), [Bu2SnCl(2-SpyO)] (3), [Ph2SnCl(2-SpyO)] (4), and [(PhCH2)2SnCl(2- SpyO)] (5). The new complexes have been characterized by elemental analysis and IR and NMR (1H, 119Sn, and 13C) spectroscopy. On the basis of 119Sn NMR data the effective coordination number in solution is five. The structures 1 and 4 have been confirmed by X-ray crystallography. Crystals of 1 are triclinic with space group P[Formula: see text] and those of 4 are monoclinic, P21/n.

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4

Abbas, Zahoor, Manoj Kumar, Hardeep Singh Tuli, et al. "Synthesis, Structural Investigations, and In Vitro/In Silico Bioactivities of Flavonoid Substituted Biguanide: A Novel Schiff Base and Its Diorganotin (IV) Complexes." Molecules 27, no. 24 (2022): 8874. http://dx.doi.org/10.3390/molecules27248874.

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Quercetin is one of the most powerful bioactive dietary flavonoids. The in vivo biological study of quercetin is extremely difficult due to its very low solubility. However, diorganotin complexes of quercetin are more useful when contrasted with quercetin due to increased solubility. In the present study, quercetin, substituted biguanide synthesized in the form of Schiff base and its di-alkyl/aryl tin (IV) complexes were obtained by condensing Schiff base with respective di-alkyl/aryl tin (IV) dichloride. Advanced analytical techniques were used for structural elucidation. The results of biolo

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5

PADAM, NABH NAGAR. "Addition Complexes of Dialkyl Phosphonates with Tin(IV) and Organotin(IV) Chlorides." Journal of Indian Chemical Society Vol. 67, Sep 1990 (1990): 703–5. https://doi.org/10.5281/zenodo.6204126.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 <em>Manuscript received 15 May 1989, revised 19 February 1990, accepted 11 May 1990</em> Addition complexes of dialkyl phosphonates with tin(IV) chloride, diorganotin dichloride and triorganotin chloride have been prepared and characterised on the basis of ir and nmr (<sup>1</sup>H, <sup>31</sup>P and <sup>1 1 9</sup>Sn) spectral data. Dialkyl phosphonates are bound to the metal atom via the phosphoryl (P = O) oxygen and the effectiveness of coordination depends upon the donor strength of the ligand and the environment of the cen

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6

Mahmoudpour, Asiyeh, Shohreh Nafisi, Ezzatollah Najafi, and Behrouz Notash. "Synthesis, characterization and electroluminescence properties of a new mixed-ligand diorganotin(IV) complex." Main Group Metal Chemistry 42, no. 1 (2019): 51–59. http://dx.doi.org/10.1515/mgmc-2019-0005.

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Abstract A new mixed-ligand diorganotin(IV) complex, [μ-(4-dpe){Me2Sn(cup)2}2] (1), was synthesized by reacting dimethyltin(IV) dichloride with 1,2-di(4-pyridyl)ethylene (4-dpe) and ammonium N-Nitroso-N-phenylhydroxylamine (cup). The prepared complex was fully characterized by PXRD, 1H, 13C and 119Sn NMR, IR, and UV spectra and elemental analysis (CHN). The structural analysis of complex 1 by X-ray diffraction showed that this compound consists of centrosymmetric binuclear units that crystallize in the monoclinic system with the space group of P21/c. Thermal behavior of this complex was interr

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7

Kumar, Amal K., and Tapas K. Chattopadhyay. "Catalytic role of diorganotin dichloride in esterification of carboxylic acids." Tetrahedron Letters 28, no. 32 (1987): 3713–14. http://dx.doi.org/10.1016/s0040-4039(00)96364-0.

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8

Dey, Dilip Kumar, Brajagopal Samanta, Antonin Lycka, and Lutz Dahlenburg. "Simple Synthesis, Characterization and Structure of Diorganotin(IV) Complexes Containing the N-(2-Salicylidene)-N'-benzoylhydrazone Ligand." Zeitschrift für Naturforschung B 58, no. 4 (2003): 336–44. http://dx.doi.org/10.1515/znb-2003-0415.

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Two diorganotin(IV) complexes of general formula R2Sn[2-OC6H4CH=NDN=C(O)Ph] (R = Ph, 1; R = Me, 2) have been synthesized from the corresponding diorganotin(IV) dichloride and the Schiff base derived from salicylaldehyde and benzoyl hydrazide. The two compounds have been characterized by elemental analysis, IR and NMR (1H, 13C, 15N, 119Sn) spectra, and their structures have been confirmed by single crystal X-ray structure analysis. Crystals of complex 1 re triclinic, space group P1̄ , a = 11.1631(5), b = 13.462(2), c = 16.511(1) Å , α = 106.193(9), β = 106.379(8), γ = 94.932(8)°, Z = 4, R1 = 0.

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9

Ee Khoo, Lian, Yan Xu, Ngoh Khang Goh, Lian Sai Chia, and Lip Lin Koh. "Molecular adducts of diorganotin dichloride with N-(2-oxidoarylideneaminoacidato) diorganotin(IV) complexes. Crystal structure of [Ph2Sn(2-OC10H6CH-NCH2COO)]SnPh2Cl2." Polyhedron 16, no. 4 (1997): 573–76. http://dx.doi.org/10.1016/0277-5387(96)00334-8.

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10

Tamas, Melinda, Roxana A. Butuza, Monica Dan, and Anca Silvestru. "Diorganotin(IV) Complexes of Organoselenolato Ligands with Pyrazole Moieties—Synthesis, Structure and Properties." Molecules 30, no. 7 (2025): 1648. https://doi.org/10.3390/molecules30071648.

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Diorganotin(IV) compounds of types RR′Sn(SeCH2CH2pz)2 [R = R′ = nBu (2), Ph (3); R = 2-(Me2NCH2)C6H4, R′ = Me (4), nBu (5), Ph (6)], and RR′SnX(SeCH2CH2pz) [R = 2-(Me2NCH2)C6H4, R′ = nBu, X = Cl (7), R′ = Me, X = SCN (9)], as well as [2-(Me2NCH2)C6H4](Me)Sn(NCS)2 (8), and the tin(II) Sn(SeCH2CH2pz)2 (10) (pz = pyrazole), were prepared by salt metathesis reactions between the appropriate diorganotin(IV) dichloride or dipseudohalide and Na[SeCH2CH2pz], with the latter freshly prepared from (pzCH2CH2)2Se2 (1). The solution behaviour of these compounds was investigated by multinuclear NMR (1H, 13C

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