Relevant bibliographies by topics / Stannoxanes

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Stannoxanes'

Author: Grafiati
Published: 18 May 2024

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Journal articles on the topic "Stannoxanes"

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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Abstract:
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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Dissertations / Theses on the topic "Stannoxanes"

1

Ahmad, Syed Usman [Verfasser]. "Synthesis, structure and reactivity of well defined stannoxanes, indoxanes and thalloxanes / S. Usman Ahmad." 2011. http://d-nb.info/1014035015/34.

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Book chapters on the topic "Stannoxanes"

1

Moloney, M. G., and M. Yaqoob. "Alcohols by Cleavage of Stannoxanes." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00732.

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You might also be interested in the extended bibliographies on the topic 'Stannoxanes' for particular source types:
Journal articles
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