par Brouwer, Frank;Alma, Jan;Valkenier, Hennie
;Voortman, Thomas P.;Hillebrand, Jorrit;Chiechi, Ryan C.;Hummelen, Jan C.
Référence Journal of materials chemistry, 21, page (1582-1592)
Publication Publié, 2010-10-11

Référence Journal of materials chemistry, 21, page (1582-1592)
Publication Publié, 2010-10-11
Article révisé par les pairs
Résumé : | We demonstrate the use of bis(pinacolato)diboron to directly polymerize symmetric, bisbromo, thiophene-based monomers via a Suzuki homo-polymerization to form co-polymers in less steps than the corresponding co-polymerization. We compare this method to the commonly used Stille co-polymerization by preparing four thiophene-based co-polymers using both methods. We use MALDI-TOF mass spectrometry to show that this new method produces high-quality, uniform polymers with narrow distributions of end-groups. By varying the electronegativity of the monomers, we demonstrate rudimentary control over these end-groups, forming either bis-H-, mono-H-mono-Br-, or bis-Br-terminated polymers in order of increasing electronegativity. |