Carboranyl Substituted Siloxanes and Octasilsesquioxanes: Synthesis, Characterization, and Reactivity
Carboranyl-containing disiloxane, cyclic-siloxane and cage-like silsesquioxane have been prepared in high yields. Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane pr...
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Veröffentlicht in: | Macromolecules 2008-11, Vol.41 (22), p.8458-8466 |
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container_title | Macromolecules |
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creator | González-Campo, Arántzazu Juárez-Pérez, Emilio José Viñas, Clara Boury, Bruno Sillanpää, Reijo Kivekäs, Raikko Núñez, Rosario |
description | Carboranyl-containing disiloxane, cyclic-siloxane and cage-like silsesquioxane have been prepared in high yields. Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane precursors and a nonhydrolytic route based on the specific reactivity of chorosilane toward DMSO. Based on the typical reactivity of the carboranyl group toward nucleophiles, dianionic disiloxanes and octaanionic silsesquioxanes were obtained without modification of the siloxane bond. Products are fully characterized by FTIR, NMR and MALDI-TOF methods. |
doi_str_mv | 10.1021/ma801483c |
format | Article |
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Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane precursors and a nonhydrolytic route based on the specific reactivity of chorosilane toward DMSO. Based on the typical reactivity of the carboranyl group toward nucleophiles, dianionic disiloxanes and octaanionic silsesquioxanes were obtained without modification of the siloxane bond. 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Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane precursors and a nonhydrolytic route based on the specific reactivity of chorosilane toward DMSO. Based on the typical reactivity of the carboranyl group toward nucleophiles, dianionic disiloxanes and octaanionic silsesquioxanes were obtained without modification of the siloxane bond. Products are fully characterized by FTIR, NMR and MALDI-TOF methods.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma801483c</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2302-6740</orcidid></addata></record> |
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source | American Chemical Society Journals |
subjects | Applied sciences Chemical Sciences Coordination chemistry Exact sciences and technology Inorganic and organomineral polymers Material chemistry Physicochemistry of polymers Polymers Preparation |
title | Carboranyl Substituted Siloxanes and Octasilsesquioxanes: Synthesis, Characterization, and Reactivity |
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