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http://hdl.handle.net/1942/2913
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DC Field | Value | Language |
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dc.contributor.author | LUTSEN, Laurence | - |
dc.contributor.author | VAN BREEMEN, ALBERT | - |
dc.contributor.author | Kreuder, W | - |
dc.contributor.author | VANDERZANDE, Dirk | - |
dc.contributor.author | GELAN, Jan | - |
dc.date.accessioned | 2007-11-20T12:53:01Z | - |
dc.date.available | 2007-11-20T12:53:01Z | - |
dc.date.issued | 2000 | - |
dc.identifier.citation | HELVETICA CHIMICA ACTA, 83(12). p. 3113-3121 | - |
dc.identifier.issn | 0018-019X | - |
dc.identifier.uri | http://hdl.handle.net/1942/2913 | - |
dc.description.abstract | A new and convenient route to an unsymmetrically substituted sulfinyl monomer of precursor polymer toward poly[2-methyl-5-(3,7-dimethyloctyloxy)-p-phenylenevinyline] (OC1C10) is described. OC1C10 is a commercial polymer used as the active layer in LEDs. Therefore, the optimization of the reaction conditions of the monomer synthesis was of some importance for a possible commercialization of this new process. It was possible to increase the overall yield by a factor of 1.5, as compared to the route previously used to obtain these compounds. | - |
dc.language.iso | en | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.title | Highly selective route to unsymmetrically substituted 1-{2-[(butylsulfanyl)methyl]-5-(chloromethyl)-4-methoxyphenoxy}-3,7-dime thyloctane and isomers toward synthesis of conjugated polymer OC1C10 used in LEDs: Synthesis and optimization | - |
dc.type | Journal Contribution | - |
dc.identifier.epage | 3121 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | 3113 | - |
dc.identifier.volume | 83 | - |
local.format.pages | 9 | - |
local.bibliographicCitation.jcat | A1 | - |
dc.description.notes | Limburgs Univ Ctr, Mat Res Inst, Div Chem, Lab Organ & Polymer Chem, B-3590 Diepenbeek, Belgium. Covion Organ Semicond GMBH, D-65926 Frankfurt, Germany.Vanderzande, DJM, Limburgs Univ Ctr, Mat Res Inst, Div Chem, Lab Organ & Polymer Chem, Univ Campus, B-3590 Diepenbeek, Belgium. | - |
local.type.refereed | Refereed | - |
local.type.specified | Article | - |
dc.bibliographicCitation.oldjcat | A1 | - |
dc.identifier.isi | 000166311000003 | - |
item.accessRights | Closed Access | - |
item.contributor | LUTSEN, Laurence | - |
item.contributor | VAN BREEMEN, ALBERT | - |
item.contributor | Kreuder, W | - |
item.contributor | VANDERZANDE, Dirk | - |
item.contributor | GELAN, Jan | - |
item.fulltext | No Fulltext | - |
item.fullcitation | LUTSEN, Laurence; VAN BREEMEN, ALBERT; Kreuder, W; VANDERZANDE, Dirk & GELAN, Jan (2000) Highly selective route to unsymmetrically substituted 1-{2-[(butylsulfanyl)methyl]-5-(chloromethyl)-4-methoxyphenoxy}-3,7-dime thyloctane and isomers toward synthesis of conjugated polymer OC1C10 used in LEDs: Synthesis and optimization. In: HELVETICA CHIMICA ACTA, 83(12). p. 3113-3121. | - |
item.validation | ecoom 2002 | - |
Appears in Collections: | Research publications |
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