Статті в журналах з теми "Stannoxanes"
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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.
Повний текст джерелаDanish, 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.
Повний текст джерелаPadělková, 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.
Повний текст джерелаSinghal, 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.
Повний текст джерелаChandrasekhar, 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.
Повний текст джерелаKraus, 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.
Повний текст джерелаMoraru, 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.
Повний текст джерелаKRAUS, 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.
Повний текст джерелаPlasseraud, 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.
Повний текст джерелаNomura, 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.
Повний текст джерелаNOMURA, 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.
Повний текст джерелаKundu, 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.
Повний текст джерелаKumar, Muthiah Senthil, Shailesh Upreti, Hanuman P. Gupta та 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, № 22 (листопад 2006): 4708–16. http://dx.doi.org/10.1016/j.jorganchem.2006.07.015.
Повний текст джерелаChandra, 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.
Повний текст джерелаDuhayon, 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.
Повний текст джерелаPadělková, 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.
Повний текст джерелаChandrasekhar, 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.
Повний текст джерелаHahn, 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.
Повний текст джерелаTiekink, 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.
Повний текст джерелаChauhan, 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.
Повний текст джерелаKundu, 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.
Повний текст джерелаStrachota, 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.
Повний текст джерелаValcarcel, 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.
Повний текст джерелаChandrasekhar, 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.
Повний текст джерелаKundu, 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, no. 10 (January 20, 2012): 2787–91. http://dx.doi.org/10.1002/chem.201102326.
Повний текст джерелаSanz, 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.
Повний текст джерелаRodzeń, 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.
Повний текст джерелаSharma, 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.
Повний текст джерелаChandrasekhar, 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.
Повний текст джерелаKhan, 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.
Повний текст джерелаButler, Patrick. "Bis(μ2-4-nitrophenolato)bis(4-nitrophenolato)di-μ3-oxido-octaphenyltetratin chloroform sesquisolvate [+ solvate]: a tetranuclear stannoxane". IUCrData 4, № 8 (6 серпня 2019). http://dx.doi.org/10.1107/s2414314619010678.
Повний текст джерелаChandrasekhar, 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.
Повний текст джерела