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Journal articles on the topic 'Stannoxanes'

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Published: 18 May 2024

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1

Fedoseevskii, V. V., and V. S. Tikhonov. "Synthesis of Polyphenylsiloxane Stannoxanes." International Polymer Science and Technology 29, no. 2 (February 2002): 50–51. http://dx.doi.org/10.1177/0307174x0202900209.

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2

Danish, Muhammad, Saqib Ali, and Muhammad Mazhar. "Fluxional behavior in dimeric tetraorganodicarboxylato stannoxanes." Heteroatom Chemistry 7, no. 4 (1996): 233–37. http://dx.doi.org/10.1002/(sici)1098-1071(199608)7:4<233::aid-hc4>3.0.co;2-6.

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3

Padělková, Zdeňka, Mikhail S. Nechaev, Zdeněk Černošek, Jiří Brus, and Aleš Růžička. "Solvent-Controlled Ring Size in Double C,N-Chelated Stannoxanes⊥." Organometallics 27, no. 20 (October 27, 2008): 5303–8. http://dx.doi.org/10.1021/om800476r.

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4

Singhal, Kiran, Subhas Kumar Chaudhary, and Om Prakash. "Action of Metal and Organometallic Halides and Pseudohalides Towards Stannoxanes." Asian Journal of Chemistry 25, no. 16 (2013): 9020–22. http://dx.doi.org/10.14233/ajchem.2013.14969.

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5

Chandrasekhar, Vadapalli, Kandasamy Gopal, Loganathan Nagarajan, Palani Sasikumar, and Pakkirisamy Thilagar. "Stannoxanes and phosphonates: New approaches in organometallic and transition metal assemblies." Journal of Chemical Sciences 118, no. 6 (November 2006): 455–62. http://dx.doi.org/10.1007/bf02703942.

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6

Kraus, George A., and Brian M. Watson. "The synthesis of Z-allylic alcohols via palladium-mediated reactions of stannoxanes with aryl halides." Tetrahedron Letters 37, no. 30 (July 1996): 5287–88. http://dx.doi.org/10.1016/0040-4039(96)01093-3.

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7

Moraru, Ionuţ-Tudor, Petronela M. Petrar, and Gabriela Nemeş. "Bridging a Knowledge Gap from Siloxanes to Germoxanes and Stannoxanes. A Theoretical Natural Bond Orbital Study." Journal of Physical Chemistry A 121, no. 12 (March 22, 2017): 2515–22. http://dx.doi.org/10.1021/acs.jpca.7b01208.

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8

KRAUS, G. A., and B. M. WATSON. "ChemInform Abstract: The Synthesis of Z-Allylic Alcohols via Palladium-Mediated Reactions of Stannoxanes with Aryl Halides." ChemInform 27, no. 46 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199646095.

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9

Plasseraud, Laurent. "CO2 Derivatives of Molecular Tin Compounds. Part 1: Hemicarbonato and Carbonato Complexes." Inorganics 8, no. 5 (April 29, 2020): 31. http://dx.doi.org/10.3390/inorganics8050031.

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This review focuses on organotin compounds bearing hemicarbonate and carbonate ligands, and whose molecular structures have been previously resolved by single-crystal X-ray diffraction analysis. Most of them were isolated within the framework of studies devoted to the reactivity of tin precursors with carbon dioxide at atmospheric or elevated pressure. Alternatively, and essentially for the preparation of some carbonato derivatives, inorganic carbonate salts such as K2CO3, Cs2CO3, Na2CO3 and NaHCO3 were also used as coreagents. In terms of the number of X-ray structures, carbonate compounds are the most widely represented (to date, there are 23 depositions in the Cambridge Structural Database), while hemicarbonate derivatives are rarer; only three have so far been characterized in the solid-state, and exclusively for diorganotin complexes. For each compound, the synthesis conditions are first specified. Structural aspects involving, in particular, the modes of coordination of the hemicarbonato and carbonato moieties and the coordination geometry around tin are then described and illustrated (for most cases) by showing molecular representations. Moreover, when they were available in the original reports, some characteristic spectroscopic data are also given for comparison (in table form). Carbonato complexes are arbitrarily listed according to their decreasing number of hydrocarbon substituents linked to tin atoms, namely tri-, di-, and mono-organotins. Four additional examples, involving three CO2 derivatives of C,N-chelated stannoxanes and one of a trinuclear nickel cluster Sn-capped, are also included in the last part of the chapter.

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10

Nomura, Ryoki, Satoru Fujii, and Haruo Matsuda. "Unusual addition of the indium-butyl bond to organotin oxides. Preparation and characterization of novel dibutylindio- or butyl(propionyloxy)indio-substituted stannoxanes." Inorganic Chemistry 29, no. 22 (October 1990): 4586–88. http://dx.doi.org/10.1021/ic00347a053.

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11

NOMURA, R., S. FUJII, and H. MATSUDA. "ChemInform Abstract: Unusual Addition of the Indium-Butyl Bond to Organotin Oxides. Preparation and Characterization of Novel Dibutylindio- or Butyl( propionyloxy)indio-Substituted Stannoxanes." ChemInform 22, no. 8 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199108266.

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12

Kundu, Subrata, Chandrajeet Mohapatra, and Vadapalli Chandrasekhar. "Cyclophosphazene–organostannoxane hybrid motifs in polymeric and molecular systems." RSC Adv. 4, no. 96 (2014): 53662–64. http://dx.doi.org/10.1039/c4ra09371b.

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13

Kumar, Muthiah Senthil, Shailesh Upreti, Hanuman P. Gupta, and Anil J. Elias. "Reactions of [η5-carboxycyclopentadiene][η4-tetraphenylcyclo butadiene] cobalt with alkyl and aryl tin oxides: Synthesis, structural studies and electrochemistry of novel monomeric and dimeric [η5-carboxycyclopentadiene][η4-tetraphenylcyclobutadiene]cobalt based stannoxanes." Journal of Organometallic Chemistry 691, no. 22 (November 2006): 4708–16. http://dx.doi.org/10.1016/j.jorganchem.2006.07.015.

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14

Chandra, Anirban, Stefan Mebs, Subrata Kundu, Uwe Kuhlmann, Peter Hildebrandt, Holger Dau, and Kallol Ray. "Catalytic dioxygen reduction mediated by a tetranuclear cobalt complex supported on a stannoxane core." Dalton Transactions 49, no. 18 (2020): 6065–73. http://dx.doi.org/10.1039/d0dt00475h.

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15

Duhayon, C., U. Hahn, A. Gégout, Y. Coppel, A. Saquet, and J. F. Nierengarten. "Self-assembled fullerene-rich stannoxane derivatives." Acta Crystallographica Section A Foundations of Crystallography 63, a1 (August 22, 2007): s160. http://dx.doi.org/10.1107/s0108767307096420.

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16

Padělková, Zdeňka, Hana Vaňkátová, Ivana Císařová, Mikhail S. Nechaev, Thomas A. Zevaco, Olaf Walter, and Aleš Růžička. "Reactivity of a C,N-Chelated Stannoxane†." Organometallics 28, no. 8 (April 27, 2009): 2629–32. http://dx.doi.org/10.1021/om801037b.

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17

Chandrasekhar, Vadapalli, Selvarajan Nagendran, Ramachandran Azhakar, Murugaeson Ravi Kumar, Alagar Srinivasan, Kallol Ray, Tavarekere K. Chandrashekar, et al. "A Lipophilic Hexaporphyrin Assembly Supported on a Stannoxane Core." Journal of the American Chemical Society 127, no. 8 (March 2005): 2410–11. http://dx.doi.org/10.1021/ja043748g.

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18

Hahn, Uwe, Aline Gégout, Carine Duhayon, Yannick Coppel, Alix Saquet, and Jean-François Nierengarten. "Self-assembly of fullerene-rich nanostructures with a stannoxane core." Chem. Commun., no. 5 (2007): 516–18. http://dx.doi.org/10.1039/b614009b.

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19

Tiekink, E. R. T. "A dimeric stannoxane structure: [Sn2(Cl)(O)(OH)(C6H5)4]2.2C3H7NO." Acta Crystallographica Section C Crystal Structure Communications 47, no. 3 (March 15, 1991): 661–62. http://dx.doi.org/10.1107/s0108270190009787.

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20

Chauhan, Mala, and Farukh Arjmand. "Stannoxane capping derived from chiral tridentate NNO donor ligand for nickel and copper macrocycles: Comparative binding studies of stannoxane moiety and its modulated copper complex with CTDNA." Journal of Organometallic Chemistry 692, no. 23 (November 2007): 5156–64. http://dx.doi.org/10.1016/j.jorganchem.2007.07.044.

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21

Kundu, Subrata, Ramesh K. Metre, Rajeev Yadav, Pratik Sen, and Vadapalli Chandrasekhar. "Multi-Pyrene Assemblies Supported on Stannoxane Frameworks: Synthesis, Structure and Photophysical Studies." Chemistry - An Asian Journal 9, no. 5 (March 11, 2014): 1403–12. http://dx.doi.org/10.1002/asia.201400054.

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22

Strachota, Adam, François Ribot, Libor Matějka, Paul Whelan, Larisa Starovoytova, Josef Pleštil, Miloš Steinhart, et al. "Preparation of Novel, Nanocomposite Stannoxane-Based Organic–Inorganic Epoxy Polymers containing Ionic bonds." Macromolecules 45, no. 1 (December 13, 2011): 221–37. http://dx.doi.org/10.1021/ma201178j.

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23

Valcarcel, José Antonio, Rodrigo Said Razo-Hernández, Laura Leticia Valdez-Velázquez, Manuel Villanueva García, Ángel Andrés Ramos Organillo, Oscar F. Vázquez-Vuelvas, Miguel A. García Ruiz, and Zeferino Gómez-Sandoval. "Antitumor structure–activity relationship in bis-stannoxane derivatives from pyridine dicarboxylic and benzoic acids." Inorganica Chimica Acta 392 (September 2012): 229–35. http://dx.doi.org/10.1016/j.ica.2012.06.029.

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24

Chandrasekhar, Vadapalli, Pakkirisamy Thilagar, Alexander Steiner, and Jamie F. Bickley. "Inorganic-Cored Photoactive Assemblies: Synthesis, Structure, and Photochemical Investigations on Stannoxane-Supported Multifluorene Compounds." Chemistry - A European Journal 12, no. 34 (November 24, 2006): 8847–61. http://dx.doi.org/10.1002/chem.200600556.

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25

Kundu, Subrata, Eduard Matito, Stephan Walleck, Florian F. Pfaff, Florian Heims, Battist Rábay, Josep M. Luis, et al. "OO Bond Formation Mediated by a Hexanuclear Iron Complex Supported on a Stannoxane Core." Chemistry - A European Journal 18, no. 10 (January 20, 2012): 2787–91. http://dx.doi.org/10.1002/chem.201102326.

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26

Sanz, Ana M., Pilar Navarro, Fernando Gomez-Contreras, Mercedes Pardo, Gèrard Pèpe, and André Samat. "A new diaza heteroaromatic crown of 3,5-disubstituted 1H-pyrazole which forms solid dinuclear complexes with lipophilic phenethylamines." Canadian Journal of Chemistry 76, no. 8 (August 1, 1998): 1174–79. http://dx.doi.org/10.1139/v98-117.

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The cyclic stannoxane obtained from N-methyldiethanolamine and dibutyltin oxide reacts with 1H-pyrazole-3,5-dicarbonyl dichloride to afford the new 26-membered diaza tetraester crown 3. In neutral medium, the above crown forms 1:2 solid dinuclear complexes with phenethylamine (3a) and homoveratrylamine (3b), which, after crystallization from acetonitrile, were isolated in high yield (90% and 85%, respectively). The 3, 3a, and 3b structures were identified from their analytical and spectroscopic (1H, 13C NMR, and MS (FAB)) data. The spectroscopic properties of 3a and 3b are demonstrating that, in each complexation centre, simultaneously to the strong participation of the four pyrazole nitrogens, an additional weaker interaction between the aliphatic nitrogen of the side chain and the amine is involved. Comparison of the total interaction energies calculated (GenMol software) for phenethylamine-derived complex (3a) and homoveratrylamine-derived one (3b) suggests that the o-dimethoxy substitution of the guest aromatic ring could be improving the stability of 3b in relation to 3a.Key words: diazacrown, 1H-pyrazole, dinuclear, complexes, phenethylamines.

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27

Rodzeń, Krzysztof, Adam Strachota, Vladimír Raus, and Ewa Pavlova. "Polyhedral oligomeric butyl stannoxane cages (Sn-POSS) as oxidation-activated linear repairing units or crosslinking nano-building blocks, depending on structure of the polymer matrix." Polymer Degradation and Stability 142 (August 2017): 1–20. http://dx.doi.org/10.1016/j.polymdegradstab.2017.05.019.

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28

Sharma, Vinita, Sangeeta Agrawal, Rakesh Bohra, Raju Ratnani, John E. Drake, Ann L. Bingham, Michael B. Hursthouse, and Mark E. Light. "Synthesis and characterization of some monoorganotin(IV) chloride adducts with internally functionalized oximes: Crystal and molecular structures of nBuSnCl3·HONC(Me)Py-2·C6H5Me and a trinuclear hydroxo bridged stannoxane {nBuSnCl2(ONC(Me)Py-2)OH}2SnnBuCl·0.5HONC(Me)Py-2." Inorganica Chimica Acta 359, no. 5 (March 2006): 1404–12. http://dx.doi.org/10.1016/j.ica.2005.09.017.

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29

Chandrasekhar, Vadapalli, Kandasamy Gopal, Loganathan Nagarajan, Palani Sasikumar, and Pakkirisamy Thilagar. "Stannoxanes and Phosphonates: New Approaches in Organometallic and Transition Metal Assemblies." ChemInform 38, no. 38 (September 18, 2007). http://dx.doi.org/10.1002/chin.200738247.

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30

Khan, Μ. I., Saima Gul, Musa Kaleem Baloch, and Wilayat Ahmed. "Synthesis and Characterization of New Dicarboxylatotetra-N-Butyl-Di-Stannoxanes Dimers Formed with N-Maleimido-Protected Amino Acids." Main Group Metal Chemistry 31, no. 5 (January 2008). http://dx.doi.org/10.1515/mgmc.2008.31.5.253.

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31

Butler, Patrick. "Bis(μ2-4-nitrophenolato)bis(4-nitrophenolato)di-μ3-oxido-octaphenyltetratin chloroform sesquisolvate [+ solvate]: a tetranuclear stannoxane." IUCrData 4, no. 8 (August 6, 2019). http://dx.doi.org/10.1107/s2414314619010678.

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The title tetranuclear stannoxane, [Sn4(C6H5)8(C6H4NO3)4O2]·1.5CHCl3·solvent, crystallized with two independent complex molecules, A and B, in the asymmetric unit together with 1.5 molecules of chloroform. There is also a region of disordered electron density, which was corrected for using the SQUEEZE routine [Spek (2015). Acta Cryst. C71, 9–18]. The oxo-tin core of each complex is in a planar `ladder' arrangement and each Sn atom is fivefold SnO3C2 coordinated, with one tin centre having an almost perfect square-pyramidal coordination geometry, while the other three Sn centres have distorted shapes. In the crystal, the complex molecules are arranged in layers, composed of A or B complexes, lying parallel to the bc plane. The complex molecules are linked by a number of C—H...O hydrogen bonds within the layers and between the layers, forming a supramolecular three-dimensional structure.

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32

Chandrasekhar, Vadapalli, Pakkirisamy Thilagar, Alexander Steiner, and Jamie F. Bickley. "Inorganic-Cored Photoactive Assemblies: Synthesis, Structure, and Photochemical Investigations on Stannoxane-Supported Multifluorene Compounds." Chemistry – A European Journal, August 29, 2006. http://dx.doi.org/10.1002/chem.600556.

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