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Journal articles on the topic 'Tricyclohexyltin'

Author: Grafiati

Published: 18 May 2024

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1

Tian, Lai-Jin, Yu-Xi Sun, Yi-Zhen Gao, and Guo-Ming Yang. "(4-Biphenylacetato)tricyclohexyltin(IV)." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (May 28, 2005): m1199—m1200. http://dx.doi.org/10.1107/s160053680501617x.

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2

Zheng, Xiao-Feng, Ling Yin, Xi-Cheng Liu, and Lai-Jin Tian. "μ-Sulfido-bis[tricyclohexyltin(IV)]." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (May 26, 2007): m1744. http://dx.doi.org/10.1107/s1600536807024117.

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3

Blunden, Stephen J., and Robin Hill. "Tricyclohexyltin compounds: Structural implications of 119Sn NMR chemical shifts." Inorganica Chimica Acta 98, no. 1 (March 1985): L7—L8. http://dx.doi.org/10.1016/s0020-1693(00)90737-0.

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4

TAKAMI, Katsushige, Tameo OKUMURA, Akiyoshi SUGIMAE, and Masao NAKAMOTO. "Determination of tricyclohexyltin compounds in environmental samples by GC." Bunseki kagaku 36, no. 3 (1987): 143–48. http://dx.doi.org/10.2116/bunsekikagaku.36.3_143.

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5

Linderman, Russell J., and James M. Siedlecki. "Selective Copper-Catalyzed Coupling Reactions of (α-Acetoxyhexyl)tricyclohexyltin." Journal of Organic Chemistry 61, no. 19 (January 1996): 6492–93. http://dx.doi.org/10.1021/jo961161h.

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6

SONG, Xueqing, Robert PIKE, and George ENG. "Crystal Structure of Tricyclohexyltin N,N′-Di-n-butyl-dithiocarbamate." Analytical Sciences: X-ray Structure Analysis Online 22 (2006): x137—x138. http://dx.doi.org/10.2116/analscix.22.x137.

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7

Teoh, Siang-guan, Do-seng Tan, Guan-yeow Yeap, and Hoong-kun Fun. "TRICYCLOHEXYLTIN(IV) COMPLEXES WITH PICOLINIC, NICOTINIC AND 5-BROMONICOTINIC ACIDS." Journal of Coordination Chemistry 48, no. 1 (July 1, 1999): 53–61. http://dx.doi.org/10.1080/00958979908024363.

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8

Imtiaz-ud-Din, Kieran C. Molloy, M. Mazhar, Sarim Dastgir, Saqib Ali, and Mary F. Mahon. "Some tricyclohexyltin carboxylates containing germanium: synthesis, spectral and crystallographic characterization." Applied Organometallic Chemistry 17, no. 10 (2003): 781–87. http://dx.doi.org/10.1002/aoc.504.

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9

Giordano, R., L. Ciaralli, G. Gattorta, M. Ciprotti, and S. Costantini. "Analysis of Tricyclohexyltin Hydroxide Using Zeeman Graphite Furnace Atomic Absorption Spectrometry." Microchemical Journal 49, no. 1 (February 1994): 69–77. http://dx.doi.org/10.1006/mchj.1994.1010.

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10

LINDERMAN, R. J., and J. M. SIEDLECKI. "ChemInform Abstract: Selective Copper-Catalyzed Coupling Reactions of (α-Acetoxyhexyl) tricyclohexyltin." ChemInform 28, no. 6 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199706062.

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11

Tudela, David, Ramón Fernández, Vitaly K. Belsky, and Valery E. Zavodnik. "Structural chemistry of triorganotin fluorides. The crystal structure of tricyclohexyltin fluoride revisited." J. Chem. Soc., Dalton Trans., no. 10 (1996): 2123–26. http://dx.doi.org/10.1039/dt9960002123.

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12

Duong, Quyen, Xueqing Song, Edlira Mitrojorgji, Scott Gordon, and George Eng. "Larvicidal and structural studies of some triphenyl- and tricyclohexyltin para-substituted benzoates." Journal of Organometallic Chemistry 691, no. 8 (April 2006): 1775–79. http://dx.doi.org/10.1016/j.jorganchem.2005.12.005.

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13

Ng, Seik Weng, V. G. Kumar Das, Song-Lin Li, and Thomas C. W. Mak. "μ-Oxalatobis(tricyclohexyltin), a dinuclear tin compound with isomeric pentacoordinate tin sites." Journal of Organometallic Chemistry 467, no. 1 (March 1994): 47–49. http://dx.doi.org/10.1016/0022-328x(94)88006-9.

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14

Sakho, Adama Moussa, Dafeng Du, Wenjie Li, Shuangshuang Liu, Dongsheng Zhu, and Lin Xu. "Synthesis, crystal structure, and characterization of dimeric tetraorganodistannoxane and two tricyclohexyltin carboxylates." Journal of Coordination Chemistry 63, no. 13 (July 10, 2010): 2317–27. http://dx.doi.org/10.1080/00958972.2010.500665.

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15

Tian, Laijin, Haixia Yu, Xiaoliang Zheng, and Xijie Liu. "Synthesis, crystal structure and cytotoxic activity of tricyclohexyltin complexes of benzenedioxyacetic acids." Applied Organometallic Chemistry 29, no. 11 (August 9, 2015): 725–29. http://dx.doi.org/10.1002/aoc.3357.

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16

Reuter, H. "Redetermination of the crystal structure of tricyclohexyltin(IV) iodide, [Sn(C6H11)3]I." Zeitschrift für Kristallographie - New Crystal Structures 219, no. 1-4 (April 2004): 347–48. http://dx.doi.org/10.1524/ncrs.2004.219.14.347.

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17

Tian, Laijin, Hui Cao, Shouxin Wang, Yuxi Sun, and Zhi Liu. "Synthesis, characterization, and cytotoxic activity of tricyclohexyltin(IV) carboxylates derived from cyclic dicarboxylic anhydrides." Journal of Coordination Chemistry 66, no. 4 (February 1, 2013): 624–37. http://dx.doi.org/10.1080/00958972.2013.767446.

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18

Abd Aziz, Nurul Amalina, Nur Atiyah Nadhrah Jamaludin, Normah Awang, Nurul Farahana Kamaludin, Kok Meng Chan, and Nur Najmi Mohamad Anuar. "Synthesis of New Organotin(IV) N-methyl-N-benzyl Dithiocarbamate Compounds and Cytotoxicity assessment on Human Lung Carcinoma Cell Line (A549)." Oriental Journal Of Chemistry 39, no. 4 (August 30, 2023): 835–44. http://dx.doi.org/10.13005/ojc/390403.

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Using the In-situ method, the successful synthesis of dibutyltin(IV) N-methyl-N-benzyldithiocarbamate (Compound 1) and tricyclohexyltin(IV) N-methyl-N-benzyldithiocarbamate (Compound 2) was achieved. Both compounds were characterized by the CHNS elemental analysis, FTIR, NMR spectroscopies and X-ray crystallography study. The experimental CHNS values demonstrated good congruence with the CHNS’s theoretical values of the suggested formula structures. The key infrared absorbance peaks, νC—N) and νC—N), which were found between 1475–1481 cm–1 and 971–975 cm–1, respectively. The 13C chemical shift of carbon in the NCS2 group was observed in the range of 200.66–202.32 ppm. The crystal structure of Compound 1 shows the anisobidentate’s coordination mode between the central metal of the Sn atom and the dithiocarbamate ligands. Compound 1 and Compound 2 have shown great toxicity effects against carcinoma cells in the human lung (A549) with lower IC50 values of 0.80 µM and 2.77 µM, respectively.

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19

Gan, Xian-Xue, and Liang-Fu Tang. "Synthesis and characterization of polymeric triphenyltin and cyclotetrameric tricyclohexyltin 2-(1H-imidazol-1-yl)acetates." Journal of Coordination Chemistry 64, no. 14 (July 13, 2011): 2458–65. http://dx.doi.org/10.1080/00958972.2011.600452.

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20

Sahib, I. Kabeer Ahammed, and D. Desaiah. "Inhibition of β-adrenergic stimulated calcium pump of rat cardiac sarcoplasmic reticulum by tricyclohexyltin hydroxide." Cell Biochemistry and Function 5, no. 2 (April 1987): 149–54. http://dx.doi.org/10.1002/cbf.290050211.

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21

Sahib, Kabeer I. Ahammad, and Durisala Desaiah. "Tricyclohexyltin hydroxide effects on cationic and substrate activation kinetics of beta-adrenergic–stimulated cardiac Ca2+-ATPase." Journal of Biochemical Toxicology 1, no. 4 (December 1986): 55–66. http://dx.doi.org/10.1002/jbt.2570010406.

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22

YU, Jiangxi, Yonglan FENG, Daizhi* KUANG, Fuxing ZHANG, Wujiu JIANG, and Xiaoming ZHU. "Microwave Assisted Synthesis, Structural Characterization, Thermal Stability and in vitro Anticancer Activity of Tricyclohexyltin 8-Quinolinoxide." Chinese Journal of Applied Chemistry 31, no. 08 (August 1, 2014): 937. http://dx.doi.org/10.3724/sp.j.1095.2014.30495.

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23

Ahmad, Nazni W., Tay Siew Huang, S. Balabaskaran, K. M. Lo, and V. G. Kumar Das. "Insecticidal Effects of Organotin(IV) Compounds on Plutella Xylostella (L.) Larvae. II. Inhibitory Potencies Against Acetylcholinesterase and Evidence for Synergism in Tests With Bacillus Thuringiensis(BER.) and Malathion." Metal-Based Drugs 1, no. 1 (January 1, 1994): 1–17. http://dx.doi.org/10.1155/mbd.1994.1.

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Features of pesticide synergism and acetylcholinesterase (AChE) inhibition (in vitro) were studied using a selected range of organotin compounds against the early 4th instar larvae of a highly resistant strain of the diamondback moth (DBM), Plutella xylostella, a major universal pest of cruciferous vegetables.Fourteen triorganotin compounds were evaluated for their ability to enhance the toxicity of the microbial insecticide, Bacillus thuringiensis (BT) and of the commercial insecticide, Malathion to Plutella xylostella larvae. Supplemental synergism was observed with triphenyl- and tricyclopentyltin hydroxides in combinations with Bacillus thuringiensis. Increased synergism was observed with an increase in the number of cyclopentyl groups on tin in the mixed series, CypnPh3-n SnX, where X = OH, and 1-(1,2,4-triazolyl). The combination of (p-chlorophenyl)diphenyltin N,N-dimethyldithiocarbamate at LD10 and LD25 concentrations with sublethal concentrations of Malathion as well as of tricyclohexyltin methanesulphonate at the 0.01% (w/v) concentration with Malathion exerted strong synergistic effects (supplemental synergism) with toxicity index (T.I) values of 7.2, 19.8 and 10.1, respectively.Studies on the in vitro inhibition of acetylcholinesterase prepared from the DBM larvae showed that while most of the triorganotin Compounds tested were without effect on the enzyme, compounds containing the thiocarbamylacetate or the dithiocarbamylacetate moieties demonstrated appreciable levels of inhibition, being comparable in efficacy to commercial grades of Malathion and Methomyl.

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24

Kamruddin, S. K., T. K. Chattopadhyaya, A. Roy, and E. R. T. Tierkink. "Biocidal Organotin Compounds. Part 2. Synthesis, Characterization and Biocidal Properties of Triorganotin(IV) Hydantoic Acid Derivatives and the Crystal Structures of Triphenyltin and Tricyclohexyltin Hydantoates." Applied Organometallic Chemistry 10, no. 7 (September 1996): 513–21. http://dx.doi.org/10.1002/(sici)1099-0739(199609)10:7<513::aid-aoc509>3.0.co;2-v.

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25

Molloy, Kieran C., Kieran Quill, Stephen J. Blunden, and Robin Hill. "Notes. Tin-119 and nitrogen-14 nuclear magnetic resonance and tin-119 variable-temperature Mössbauer spectroscopic study of tricyclohexyltin isothiocyanate including the first observation of resolved117,119Sn–14N coupling in an organotin compound." J. Chem. Soc., Dalton Trans., no. 4 (1986): 875–77. http://dx.doi.org/10.1039/dt9860000875.

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26

Ng, S. W. "2,2'-Iminodipyridinium(1+) dichlorotriphenylstannate and 2,2'-iminodipyridinium(1+) tricyclohexylbis(trifluoroacetato)stannate." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (September 15, 1999): IUC9900098. http://dx.doi.org/10.1107/s0108270199098923.

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27

Zhang, Hao, Haixia Yu, Xijie Liu, and Laijin Tian. "Synthesis, structural characterization, and antibacterial activity of tricyclohexyltin aryloxyacetates." Main Group Metal Chemistry 38, no. 5-6 (January 1, 2015). http://dx.doi.org/10.1515/mgmc-2015-0025.

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28

Zhang, Shuai, Wenqiang Wang, Qingtao liu, Xiaofeng Zheng, and Laijin Tian. "Synthesis, crystal structure, and antibacterial activity of tricyclohexyltin salicylates." Main Group Metal Chemistry 39, no. 3-4 (January 1, 2016). http://dx.doi.org/10.1515/mgmc-2016-0014.

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29

Biscoe, Mark, Meruyert Binayeva, Xinghua Ma, and Pejman Ghaemimohammadi. "A General Approach to Stereospecific Pd-Catalyzed Cross-Coupling Reactions of Benzylic Stereocenters." Chemical Science, 2023. http://dx.doi.org/10.1039/d3sc04519f.

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We have developed a general process for the formation of enantioenriched benzylic stereocenters via stereospecific Pd-catalyzed cross-coupling reactions of enantioenriched benzylic tricyclohexyltin nucleophiles. This process proceeds with excellent stereospecificity for...

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30

Song, Xueqing, Christopher Cahill, and George Eng. "CRYSTAL STRUCTURE OF TRICYCLOHEXYLTIN 4-HYDROXYBENZOATE." Main Group Metal Chemistry 25, no. 11 (January 2002). http://dx.doi.org/10.1515/mgmc.2002.25.11.703.

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31

Song, Xueqing, and George Eng. "Crystal Structure of Tricyclohexyltin 2,2,3,3- Tetramethylcyclopropanecarbocylate." Main Group Metal Chemistry 27, no. 5 (January 2004). http://dx.doi.org/10.1515/mgmc.2004.27.5.259.

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32

Song, Xueqing, Christopher Cahill, and George Eng. "THE CRYSTAL STRUCTURE OF TRICYCLOHEXYLTIN N-n-BUTYL DITHIOCARBAMATE." Main Group Metal Chemistry 25, no. 1-2 (January 2002). http://dx.doi.org/10.1515/mgmc.2002.25.1-2.13.

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33

Yuxing Tan, Wujiu Jiang, Yonglan Feng, Jiangxi Yu, and Daizhi Kuang. "Synthesis, Characterization, and Herbicidal Activity of Two Tricyclohexyltin Aryloxyacetates." Russian Journal of Inorganic Chemistry, June 19, 2023. http://dx.doi.org/10.1134/s003602362260294x.

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34

Clarke, David J., Dainis Dakternieks, and Edward R. T. Tiekink. "X-RAY STRUCTURE OF O,S-BIS(TRICYCLOHEXYLTIN(IV)) 2-MERCAPTOBENZOATE." Main Group Metal Chemistry 24, no. 5 (January 2001). http://dx.doi.org/10.1515/mgmc.2001.24.5.309.

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35

BLUNDEN, S. J., and R. HILL. "ChemInform Abstract: TRICYCLOHEXYLTIN COMPOUNDS: STRUCTURAL IMPLICATIONS OF TIN-119 NMR CHEMICAL SHIFTS." Chemischer Informationsdienst 16, no. 27 (July 9, 1985). http://dx.doi.org/10.1002/chin.198527047.

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36

Ng, Seik Weng. "WATER-COORDINATED TRIORGANOTIN CARBOXYLATES. CRYSTAL STRUCTURES OF BIS(TRIPHENYLTIN 3-OXAPENTAMETHYLENETHIOCARBAMOYL- S-ACETATE) HYDRATE AND TRICYCLOHEXYLTIN 3-OXAPENTAMETHYLENE-THIOCARBAMOYL- S-ACETATE HYDRATE." Main Group Metal Chemistry 19, no. 2 (January 1996). http://dx.doi.org/10.1515/mgmc.1996.19.2.113.

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37

MOLLOY, K. C., K. QUILL, S. J. BLUNDEN, and R. HILL. "ChemInform Abstract:119Sn and 14N NMR and119Sn Variable-temperature Mößbauer Spectroscopic Study of Tricyclohexyltin Isothiocyanate Including the First Observation of Resolved 117,119Sn-14N Coupling in an Organotin Compound." Chemischer Informationsdienst 17, no. 32 (August 12, 1986). http://dx.doi.org/10.1002/chin.198632060.

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