Synthesis and properties of aromatic telechelic monodisperse diols, 1. Radical‐initiated addition of 10‐undecen‐1‐ol to new aromatic α,ω‐dithiols
Identifieur interne : 000231 ( Maroc/Analysis ); précédent : 000230; suivant : 000232Synthesis and properties of aromatic telechelic monodisperse diols, 1. Radical‐initiated addition of 10‐undecen‐1‐ol to new aromatic α,ω‐dithiols
Auteurs : Bruno Améduri [France] ; Bernard Boutevin [France] ; Mohammed Khamlichi [France] ; Jean-Jacques Robin [France] ; Abderrahman El Idrissi [Maroc] ; Abdelkarim Ramdani [Maroc]Source :
- Macromolecular Chemistry and Physics [ 1022-1352 ] ; 1994-10.
Abstract
The synthesis of aromatic telechelic monodisperse diols produced from the radical‐initiated addition reaction of a two‐fold excess of 10‐undecen‐1‐ol and new α,ω‐dithiols is presented. The dithiols were prepared by esterification of thioglycolic acid with monodisperse telechelic diols obtained by fractionation of oligo(ethylene terephthalate)s and oligo(tetramethylene terephthalate)s. In all the cases, the long‐chain α,ω‐diols were produced selectively and quantitatively. The diols are soluble in most organic solvents, contrary to classical oligo(ethylene terephthalate)s and oligo(tetramethylene terephthalate)s.
Url:
DOI: 10.1002/macp.1994.021951012
Affiliations:
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<front><div type="abstract" xml:lang="en">The synthesis of aromatic telechelic monodisperse diols produced from the radical‐initiated addition reaction of a two‐fold excess of 10‐undecen‐1‐ol and new α,ω‐dithiols is presented. The dithiols were prepared by esterification of thioglycolic acid with monodisperse telechelic diols obtained by fractionation of oligo(ethylene terephthalate)s and oligo(tetramethylene terephthalate)s. In all the cases, the long‐chain α,ω‐diols were produced selectively and quantitatively. The diols are soluble in most organic solvents, contrary to classical oligo(ethylene terephthalate)s and oligo(tetramethylene terephthalate)s.</div>
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