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Synthesis of poly(5,6-difluoro-2,1,3-benzothiadiazole-alt-9,9-dioctyl-fluorene) via direct arylation polycondensation
| Content Provider | Semantic Scholar |
|---|---|
| Author | Zhang, Xiaojie Li, Sida Shi, Xin-Cui Geng, Yanhou Wang, Fosong |
| Copyright Year | 2014 |
| Abstract | Poly(5,6-difluoro-2,1,3-benzothiadiazole-alt-9,9-dioctylfluorene) was successfully synthesized via direct arylation polycondensation of 5,6-difluoro-2,1,3-benzothiadiazole and 2,7-dibromo-9,9-dioctylfluorene. The reaction conditions were optimized, and a polymer with number-average molecular weight (Mn) of 41,000 was obtained by using Pd(OAc)2, PtBu2Me-HBF4, pivalic acid, K2CO3, and toluene as catalyst, ligand, additive, base, and solvent, respectively. The polycondensation was also performed with 5,6-dioctyloxy-2,1,3-benzothiadiazole or 2,1,3-benzothiadiazole as the comonomer, and the results indicate that the introduction of electron-withdrawing fluorine atoms at the ortho-positions to the CH bonds is essential for the reactivity of the direct arylation. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 2367–2374 |
| Starting Page | 2367 |
| Ending Page | 2374 |
| Page Count | 8 |
| File Format | PDF HTM / HTML |
| DOI | 10.1002/pola.27251 |
| Volume Number | 52 |
| Alternate Webpage(s) | http://ir.ciac.jl.cn/bitstream/322003/57368/1/609.pdf |
| Alternate Webpage(s) | https://doi.org/10.1002/pola.27251 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |