A new copolymer bearing a cysteine moiety, designed for molecular interaction, metal-ion-detection, and chiral recognition, was synthesized starting from the diborom derivative of methyl N-(tert-butoxycarbonyl)-S-thien-3-ylcysteinate and distannylthiophene through a Stille coupling reaction. UV-vis spectroscopy, circular dichroism, NMR spectroscopy, and gel permeation chromatography analyses evidenced that this polymer is able to form self-assembling structures, through the formation of a hydrogen-bond network, not only in the solid state but also in solution.
A self-assembling polythiophene functionalised with a cysteine moiety / Mucci, Adele; Parenti, Francesca; Schenetti, Luisa. - In: MACROMOLECULAR RAPID COMMUNICATIONS. - ISSN 1022-1336. - STAMPA. - 24:9(2003), pp. 547-550. [10.1002/marc.200390091]
A self-assembling polythiophene functionalised with a cysteine moiety
MUCCI, Adele;PARENTI, Francesca;SCHENETTI, Luisa
2003
Abstract
A new copolymer bearing a cysteine moiety, designed for molecular interaction, metal-ion-detection, and chiral recognition, was synthesized starting from the diborom derivative of methyl N-(tert-butoxycarbonyl)-S-thien-3-ylcysteinate and distannylthiophene through a Stille coupling reaction. UV-vis spectroscopy, circular dichroism, NMR spectroscopy, and gel permeation chromatography analyses evidenced that this polymer is able to form self-assembling structures, through the formation of a hydrogen-bond network, not only in the solid state but also in solution.File | Dimensione | Formato | |
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