期刊
MACROMOLECULES
卷 48, 期 4, 页码 979-986出版社
AMER CHEMICAL SOC
DOI: 10.1021/ma502542g
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资金
- Conacyt [311311]
- Royal Society
- EPSRC [EP/K03099X/1]
- InnovateUK of the Knowledge Centre for Material Chemistry
- EPSRC [EP/K03099X/1, EP/H004408/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/K03099X/1, EP/H004408/1] Funding Source: researchfish
The synthesis of highly regioregular poly(3-hexylthiophene-2,5-diyl), rr-P3HT, by Suzuki-Miyaura polymerization is reported. The key N-methyliminodiacetic acid (MIDA) boronate ester thienyl monomer was synthesized using a one-pot multigram scale procedure, in high purity, and in good isolated yield (80%) by direct electrophilic borylation. Conditions for the hydrolysis of the MIDA protecting group and the polymerization reaction were investigated. The optimal procedure gave rr-P3HT with >98% HT couplings, excellent isolated yields (up to 94%), and polymer molecular weights up to M-n = 18.7 kDa and M-w = 42.7 kDa. The performance of the MIDA containing monomer was compared to that of the pinacol boronate ester under identical polymerization conditions, with the latter producing lower molecular weight polymers in reduced yield.
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