Silica dissolution as a route to octaanionic silsesquioxanes
dc.contributor.author | Kang, K. H. | en_US |
dc.contributor.author | Laine, Richard M. | en_US |
dc.date.accessioned | 2007-07-11T18:15:33Z | |
dc.date.available | 2007-07-11T18:15:33Z | |
dc.date.issued | 2006-06 | en_US |
dc.identifier.citation | Kang, K. H.; Laine, R. M. (2006). "Silica dissolution as a route to octaanionic silsesquioxanes." Applied Organometallic Chemistry 20(6): 393-398. <http://hdl.handle.net/2027.42/55232> | en_US |
dc.identifier.issn | 0268-2605 | en_US |
dc.identifier.issn | 1099-0739 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/55232 | |
dc.description.abstract | The octaanion, [OSiO 1.5 ] 8 8− (OA) is a low cost, discrete nano silica particle that can be made directly from high surface area, amorphous silica reacted with Me 4 NOH in water alcohol mixtures. It would be ideal if Me 4 NOH could be formed in situ from, for example, Me 4 NCl and NaOH, as long known in the literature. This process would reduce costs and enable recycling of Me 4 NCl produced in the functionalization of OA with chlorosilanes, RMe 2 SiCl, to form [RMe 2 SiOSiO 1.5 ] 8 organic/inorganic hybrid nanobuilding blocks. Kinetic studies were conducted to assess base-promoted dissolution of fumed silica (25 m 2 /g) as a function of concentrations, times, etc., to form the octaanion [OSiO 1.5 ] 8 8− using Me 4 NOH, NaOH and mixtures of NaOH/Me 4 NCl. Surprisingly, we find that small amounts of Me 4 NCl greatly inhibit the dissolution reaction for reasons that are as yet unknown. Copyright © 2005 John Wiley & Sons, Ltd. | en_US |
dc.format.extent | 141234 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | John Wiley & Sons, Ltd. | en_US |
dc.subject.other | Chemistry | en_US |
dc.subject.other | Industrial Chemistry and Chemical Engineering | en_US |
dc.title | Silica dissolution as a route to octaanionic silsesquioxanes | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbsecondlevel | Chemistry | en_US |
dc.subject.hlbsecondlevel | Materials Science and Engineering | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Materials Science and Engineering, and the Macromolecular Science and Engineering Program, University of Michigan, Ann Arbor, MI 48109-2136, USA ; On leave from Korean Chemicals Company | en_US |
dc.contributor.affiliationum | Department of Materials Science and Engineering, and the Macromolecular Science and Engineering Program, University of Michigan, Ann Arbor, MI 48109-2136, USA ; This paper is dedicated to Professor Ulrich Schubert on the occasion of his 60th birthday ; University of Michigan, Ann Arbour, MI 48109-2136. | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/55232/1/1071_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/aoc.1071 | en_US |
dc.identifier.source | Applied Organometallic Chemistry | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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