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dc.contributor.authorLai, Yu-Yingen_US
dc.contributor.authorTung, Tsu-Chienen_US
dc.contributor.authorLiang, Wei-Weien_US
dc.contributor.authorCheng, Yen-Juen_US
dc.date.accessioned2015-07-21T08:29:31Z-
dc.date.available2015-07-21T08:29:31Z-
dc.date.issued2015-05-12en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.macromol.5b00488en_US
dc.identifier.urihttp://hdl.handle.net/11536/124817-
dc.description.abstractDirect C-H arylation polymerization of 2-bromo-3-1-hexylselenophene and 2-bromo-3-hexylthiophene catalyzed by N-heterocyclic carbene (NHC) palladium-based and Pd(OAc)(2)-based, systems has been carried out and investigated. Under the optimized conditions, high molecular weight poly(3-hexylthiohphene) (P3HT), (M-n=26.9K g/mol) with high head-to-tail regioregularity (94%) can he obtained by using [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloro[3-phenylallyl]-palladium(II) (Pd-IPr) 8 the catalyst. Pd-IPr exhibits a wide range of working temperatures froth 70 to 140 degrees C and good catalytic reproducibility as a result of its high thermal stability. It was found that the presence of additional phosphine ligand, such as tris(o-methoxyphenyl)phosphine,, can increase the polymerization efficiency in the Pd(OAc)2 system. This improvement is linked to the stability enhancement for the active species during the course of catalysis. For the first time, poly(3-hexylselenophene) (P3HS) was also obtained by direct-arylation polymerization in this research. The modest molecular weight is attributed to the poor solubility P3HS in the used solvents. Density-functional-theory (DFT) calculations were performed to investigate the postulated reaction mechanisms for our catalytic systems. The,experimental observations can thus be elucidated by the help of computation: Most significantly, a main-chain alternating and side-chain regioregular (RR = 94%) poly(3-hexylselenophene-alt-3-hexylthiophene) (Alt-P3HST) with high molecular weight (20.0K g/mol) was successfully synthesized via the Pd-IPr-catalyzed direct-arylation polymerization of a well-designed 2-bromo-8-hexyl-5-(3-hexylseleophen-2-yl)thiophene monomer. The molecular properties of the Alt-P3HST were characterized to compare with those of P3HT and P3HS. This research demonstrates in-depth investigation on the NHC-based palladium catalysts for the synthesis of Conjugated polymers via direct C-H bond polymerization.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of Poly(3-hexylthiophene), Poly(3-hexylselenophene), and Poly(3-hexylselenophene-alt-3-hexylthiophene) by Direct C-H Arylation Polymerization via N-Heterocyclic Carbene Palladium Catalystsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.macromol.5b00488en_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume48en_US
dc.citation.spage2978en_US
dc.citation.epage2988en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000354579000014en_US
dc.citation.woscount0en_US
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