Different radical initiation techniques of hydrosilylation reactions of multiple bonds in water: Dioxygen initiation

The relevance of radical initiation methodologies for the classical hydrosilylation reactions of organic compounds bearing C-C multiple bonds is due to the need to come up with newer and more efficient methods to effect this reaction, on account of its applications on surface chemistry. In the past,...

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Detalles Bibliográficos
Autor principal: Postigo, A.
Otros Autores: Nudelman, N.S
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2010
Acceso en línea:Registro en Scopus
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100 1 |a Postigo, A. 
245 1 0 |a Different radical initiation techniques of hydrosilylation reactions of multiple bonds in water: Dioxygen initiation 
260 |c 2010 
270 1 0 |m Postigo, A.; Faculty of Science, University of Belgrano, Villanueva 1324 CP 1426, Buenos Aires, Argentina; email: alberto.postigo@ub.edu.ar 
506 |2 openaire  |e Política editorial 
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504 |a Chatgilialoglu, C., (2004) Organosilanes in Radical Chemistry, , Wiley, Chicheter 
504 |a Postigo, A., Ferreri, C., Navacchia, M.L., Chatgilialoglu, C., (2005) Synlett, 18, p. 2854 
504 |a Postigo, A., Kopsov, S., Ferreri, C., Chatgilialoglu, C., (2007) Org. Lett., 9, p. 5159 
504 |a Postigo, A., Kopsov, S., Zlotsky, S., Ferreri, C., Chatgilialoglu, C., (2009) Orga-nometallics, 28, p. 3282 
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520 3 |a The relevance of radical initiation methodologies for the classical hydrosilylation reactions of organic compounds bearing C-C multiple bonds is due to the need to come up with newer and more efficient methods to effect this reaction, on account of its applications on surface chemistry. In the past, when organic solventswere employed, thermal and photochemical methods for the chain initiation reaction have been documented (thermal and photochemical decompositions of azo compounds). We herein present the dioxygen-initiation technique of the classical radical hydrosilylation reaction of C-C triple bonds with tris(trimethylsilyl)silane ((Me3Si)3SiH) in water. This initiation technique is confronted with the photochemical radical initiation in the absence of a chemical radical precursor other than the silane and also confronted with the classical thermal initiation triggered by the decomposition of an azo compound, both performed in water. The radical-based dioxygen initiation methodology studied in water is shown to afford the highest Z:E stereoselective ratios of hydrosilylated alkenes. Copyright © 2010 John Wiley and Sons, Ltd.  |l eng 
593 |a Faculty of Science, University of Belgrano, Villanueva 1324 CP 1426, Buenos Aires, Argentina 
593 |a Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 3er piso, CP1428, Buenos Aires, Argentina 
690 1 0 |a DIOXYGEN INITIATION 
690 1 0 |a HYDROSILYLATION 
690 1 0 |a RADICAL REACTIONS IN WATER 
690 1 0 |a REACTION MECHANISMS 
690 1 0 |a TRIS(TRIMETHYLSILYL)SILANE 
690 1 0 |a AZO COMPOUND 
690 1 0 |a CHAIN INITIATION 
690 1 0 |a CHEMICAL RADICALS 
690 1 0 |a DIOXYGENS 
690 1 0 |a EFFICIENT METHOD 
690 1 0 |a HYDROSILYLATION REACTION 
690 1 0 |a MULTIPLE BONDS 
690 1 0 |a PHOTOCHEMICAL DECOMPOSITIONS 
690 1 0 |a PHOTOCHEMICAL METHOD 
690 1 0 |a RADICAL INITIATIONS 
690 1 0 |a RADICAL REACTIONS IN WATER 
690 1 0 |a REACTION MECHANISM 
690 1 0 |a STEREO-SELECTIVE 
690 1 0 |a THERMAL INITIATIONS 
690 1 0 |a TO EFFECT 
690 1 0 |a TRIPLE BONDS 
690 1 0 |a TRIS(TRIMETHYLSILYL)SILANE 
690 1 0 |a CHEMICAL BONDS 
690 1 0 |a HYDROSILYLATION 
690 1 0 |a OLEFINS 
690 1 0 |a REACTION KINETICS 
690 1 0 |a SURFACE CHEMISTRY 
690 1 0 |a DECOMPOSITION 
700 1 |a Nudelman, N.S. 
773 0 |d 2010  |g v. 23  |h pp. 910-914  |k n. 10  |p J Phys Org Chem  |x 08943230  |w (AR-BaUEN)CENRE-576  |t Journal of Physical Organic Chemistry 
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