Artículos de revistas sobre el tema "Stannoxanes"
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Fedoseevskii, V. V. y V. S. Tikhonov. "Synthesis of Polyphenylsiloxane Stannoxanes". International Polymer Science and Technology 29, n.º 2 (febrero de 2002): 50–51. http://dx.doi.org/10.1177/0307174x0202900209.
Texto completoDanish, Muhammad, Saqib Ali y Muhammad Mazhar. "Fluxional behavior in dimeric tetraorganodicarboxylato stannoxanes". Heteroatom Chemistry 7, n.º 4 (1996): 233–37. http://dx.doi.org/10.1002/(sici)1098-1071(199608)7:4<233::aid-hc4>3.0.co;2-6.
Texto completoPadělková, Zdeňka, Mikhail S. Nechaev, Zdeněk Černošek, Jiří Brus y Aleš Růžička. "Solvent-Controlled Ring Size in Double C,N-Chelated Stannoxanes⊥". Organometallics 27, n.º 20 (27 de octubre de 2008): 5303–8. http://dx.doi.org/10.1021/om800476r.
Texto completoSinghal, Kiran, Subhas Kumar Chaudhary y Om Prakash. "Action of Metal and Organometallic Halides and Pseudohalides Towards Stannoxanes". Asian Journal of Chemistry 25, n.º 16 (2013): 9020–22. http://dx.doi.org/10.14233/ajchem.2013.14969.
Texto completoChandrasekhar, Vadapalli, Kandasamy Gopal, Loganathan Nagarajan, Palani Sasikumar y Pakkirisamy Thilagar. "Stannoxanes and phosphonates: New approaches in organometallic and transition metal assemblies". Journal of Chemical Sciences 118, n.º 6 (noviembre de 2006): 455–62. http://dx.doi.org/10.1007/bf02703942.
Texto completoKraus, George A. y Brian M. Watson. "The synthesis of Z-allylic alcohols via palladium-mediated reactions of stannoxanes with aryl halides". Tetrahedron Letters 37, n.º 30 (julio de 1996): 5287–88. http://dx.doi.org/10.1016/0040-4039(96)01093-3.
Texto completoMoraru, Ionuţ-Tudor, Petronela M. Petrar y Gabriela Nemeş. "Bridging a Knowledge Gap from Siloxanes to Germoxanes and Stannoxanes. A Theoretical Natural Bond Orbital Study". Journal of Physical Chemistry A 121, n.º 12 (22 de marzo de 2017): 2515–22. http://dx.doi.org/10.1021/acs.jpca.7b01208.
Texto completoKRAUS, G. A. y B. M. WATSON. "ChemInform Abstract: The Synthesis of Z-Allylic Alcohols via Palladium-Mediated Reactions of Stannoxanes with Aryl Halides." ChemInform 27, n.º 46 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199646095.
Texto completoPlasseraud, Laurent. "CO2 Derivatives of Molecular Tin Compounds. Part 1: Hemicarbonato and Carbonato Complexes". Inorganics 8, n.º 5 (29 de abril de 2020): 31. http://dx.doi.org/10.3390/inorganics8050031.
Texto completoNomura, Ryoki, Satoru Fujii y 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, n.º 22 (octubre de 1990): 4586–88. http://dx.doi.org/10.1021/ic00347a053.
Texto completoNOMURA, R., S. FUJII y 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, n.º 8 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199108266.
Texto completoKundu, Subrata, Chandrajeet Mohapatra y Vadapalli Chandrasekhar. "Cyclophosphazene–organostannoxane hybrid motifs in polymeric and molecular systems". RSC Adv. 4, n.º 96 (2014): 53662–64. http://dx.doi.org/10.1039/c4ra09371b.
Texto completoKumar, Muthiah Senthil, Shailesh Upreti, Hanuman P. Gupta y 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, n.º 22 (noviembre de 2006): 4708–16. http://dx.doi.org/10.1016/j.jorganchem.2006.07.015.
Texto completoChandra, Anirban, Stefan Mebs, Subrata Kundu, Uwe Kuhlmann, Peter Hildebrandt, Holger Dau y Kallol Ray. "Catalytic dioxygen reduction mediated by a tetranuclear cobalt complex supported on a stannoxane core". Dalton Transactions 49, n.º 18 (2020): 6065–73. http://dx.doi.org/10.1039/d0dt00475h.
Texto completoDuhayon, C., U. Hahn, A. Gégout, Y. Coppel, A. Saquet y J. F. Nierengarten. "Self-assembled fullerene-rich stannoxane derivatives". Acta Crystallographica Section A Foundations of Crystallography 63, a1 (22 de agosto de 2007): s160. http://dx.doi.org/10.1107/s0108767307096420.
Texto completoPadělková, Zdeňka, Hana Vaňkátová, Ivana Císařová, Mikhail S. Nechaev, Thomas A. Zevaco, Olaf Walter y Aleš Růžička. "Reactivity of a C,N-Chelated Stannoxane†". Organometallics 28, n.º 8 (27 de abril de 2009): 2629–32. http://dx.doi.org/10.1021/om801037b.
Texto completoChandrasekhar, 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, n.º 8 (marzo de 2005): 2410–11. http://dx.doi.org/10.1021/ja043748g.
Texto completoHahn, Uwe, Aline Gégout, Carine Duhayon, Yannick Coppel, Alix Saquet y Jean-François Nierengarten. "Self-assembly of fullerene-rich nanostructures with a stannoxane core". Chem. Commun., n.º 5 (2007): 516–18. http://dx.doi.org/10.1039/b614009b.
Texto completoTiekink, E. R. T. "A dimeric stannoxane structure: [Sn2(Cl)(O)(OH)(C6H5)4]2.2C3H7NO". Acta Crystallographica Section C Crystal Structure Communications 47, n.º 3 (15 de marzo de 1991): 661–62. http://dx.doi.org/10.1107/s0108270190009787.
Texto completoChauhan, Mala y 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, n.º 23 (noviembre de 2007): 5156–64. http://dx.doi.org/10.1016/j.jorganchem.2007.07.044.
Texto completoKundu, Subrata, Ramesh K. Metre, Rajeev Yadav, Pratik Sen y Vadapalli Chandrasekhar. "Multi-Pyrene Assemblies Supported on Stannoxane Frameworks: Synthesis, Structure and Photophysical Studies". Chemistry - An Asian Journal 9, n.º 5 (11 de marzo de 2014): 1403–12. http://dx.doi.org/10.1002/asia.201400054.
Texto completoStrachota, 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, n.º 1 (13 de diciembre de 2011): 221–37. http://dx.doi.org/10.1021/ma201178j.
Texto completoValcarcel, 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 y Zeferino Gómez-Sandoval. "Antitumor structure–activity relationship in bis-stannoxane derivatives from pyridine dicarboxylic and benzoic acids". Inorganica Chimica Acta 392 (septiembre de 2012): 229–35. http://dx.doi.org/10.1016/j.ica.2012.06.029.
Texto completoChandrasekhar, Vadapalli, Pakkirisamy Thilagar, Alexander Steiner y Jamie F. Bickley. "Inorganic-Cored Photoactive Assemblies: Synthesis, Structure, and Photochemical Investigations on Stannoxane-Supported Multifluorene Compounds". Chemistry - A European Journal 12, n.º 34 (24 de noviembre de 2006): 8847–61. http://dx.doi.org/10.1002/chem.200600556.
Texto completoKundu, Subrata, Eduard Matito, Stephan Walleck, Florian F. Pfaff, Florian Heims, Battist Rábay, Josep M. Luis et al. "OO Bond Formation Mediated by a Hexanuclear Iron Complex Supported on a Stannoxane Core". Chemistry - A European Journal 18, n.º 10 (20 de enero de 2012): 2787–91. http://dx.doi.org/10.1002/chem.201102326.
Texto completoSanz, Ana M., Pilar Navarro, Fernando Gomez-Contreras, Mercedes Pardo, Gèrard Pèpe y 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, n.º 8 (1 de agosto de 1998): 1174–79. http://dx.doi.org/10.1139/v98-117.
Texto completoRodzeń, Krzysztof, Adam Strachota, Vladimír Raus y 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 (agosto de 2017): 1–20. http://dx.doi.org/10.1016/j.polymdegradstab.2017.05.019.
Texto completoSharma, Vinita, Sangeeta Agrawal, Rakesh Bohra, Raju Ratnani, John E. Drake, Ann L. Bingham, Michael B. Hursthouse y 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, n.º 5 (marzo de 2006): 1404–12. http://dx.doi.org/10.1016/j.ica.2005.09.017.
Texto completoChandrasekhar, Vadapalli, Kandasamy Gopal, Loganathan Nagarajan, Palani Sasikumar y Pakkirisamy Thilagar. "Stannoxanes and Phosphonates: New Approaches in Organometallic and Transition Metal Assemblies". ChemInform 38, n.º 38 (18 de septiembre de 2007). http://dx.doi.org/10.1002/chin.200738247.
Texto completoKhan, Μ. I., Saima Gul, Musa Kaleem Baloch y 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, n.º 5 (enero de 2008). http://dx.doi.org/10.1515/mgmc.2008.31.5.253.
Texto completoButler, Patrick. "Bis(μ2-4-nitrophenolato)bis(4-nitrophenolato)di-μ3-oxido-octaphenyltetratin chloroform sesquisolvate [+ solvate]: a tetranuclear stannoxane". IUCrData 4, n.º 8 (6 de agosto de 2019). http://dx.doi.org/10.1107/s2414314619010678.
Texto completoChandrasekhar, Vadapalli, Pakkirisamy Thilagar, Alexander Steiner y Jamie F. Bickley. "Inorganic-Cored Photoactive Assemblies: Synthesis, Structure, and Photochemical Investigations on Stannoxane-Supported Multifluorene Compounds". Chemistry – A European Journal, 29 de agosto de 2006. http://dx.doi.org/10.1002/chem.600556.
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