Loading…
One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer
Polycondensation of 1,2,4,5-tetrafluorobenzene (1) with 3,3′-dihexyl-2,2′-bithiophene via Pd/Ag dual-catalyzed cross-dehydrogenative coupling was examined. In situ deprotonation-metalation of 1 with Ag salt proceeded smoothly at 25 °C, and the subsequent transmetalation with a Pd catalyst provided a...
Saved in:
Published in: | Synthetic metals 2023-03, Vol.293, p.117279, Article 117279 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03 |
---|---|
cites | cdi_FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03 |
container_end_page | |
container_issue | |
container_start_page | 117279 |
container_title | Synthetic metals |
container_volume | 293 |
creator | Onda, Naoki Sato, Ryota Kuwabara, Junpei Yasuda, Takeshi Kanbara, Takaki |
description | Polycondensation of 1,2,4,5-tetrafluorobenzene (1) with 3,3′-dihexyl-2,2′-bithiophene via Pd/Ag dual-catalyzed cross-dehydrogenative coupling was examined. In situ deprotonation-metalation of 1 with Ag salt proceeded smoothly at 25 °C, and the subsequent transmetalation with a Pd catalyst provided a cross-coupling product. The sequential one-pot two-step reaction method effectively suppressed undesired homo-coupling defects during polymerization. The obtained highly regioregular polymer had a packing structure and exhibited strong fluorescence in the film state, which was also evaluated for use as an emitting material in organic light-emitting diodes.
[Display omitted]
•One-pot two-step cross-dehydrogenative-coupling polycondensation is demonstrated.•The sequential one-pot two-step reaction effectively suppressed undesired homo-coupling defects.•The regioregular polymer exhibits high crystallinity and strong fluorescence. |
doi_str_mv | 10.1016/j.synthmet.2023.117279 |
format | article |
fullrecord | <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_synthmet_2023_117279</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0379677923000012</els_id><sourcerecordid>S0379677923000012</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03</originalsourceid><addsrcrecordid>eNqFkM1qwzAQhEVpoenPKxS9gF1Jtiz71hL6B4Fc2rOQ5FXi4EhGUlJc6LvXSdpzTzuwzOzsh9AdJTkltLrf5HF0ab2FlDPCipxSwURzhma0Fk1WsIacoxkpJl0J0Vyiqxg3hBDaMD5D30sH2eATTp8-iwkGbIKPMWthPbbBr8Cp1O0hM3439J1b4cH3o_GuBRenjXfY-oCPBSB2EXuLE6SgbL_zwWtwXzAd0CpCiyfbZrdSaZKHlC2EG3RhVR_h9ndeo4_np_f5a7ZYvrzNHxeZKXiVsoawSoESipe8rrkRQthaCEU55wQ0UFrrUlfAatKWldBEMzAlLVpmmQZLimtUnXKPzwWwcgjdVoVRUiIPEOVG_kGUB4jyBHEyPpyMMLXbdxBkNB04A20XwCTZ-u6_iB9mCIPG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer</title><source>ScienceDirect Journals</source><creator>Onda, Naoki ; Sato, Ryota ; Kuwabara, Junpei ; Yasuda, Takeshi ; Kanbara, Takaki</creator><creatorcontrib>Onda, Naoki ; Sato, Ryota ; Kuwabara, Junpei ; Yasuda, Takeshi ; Kanbara, Takaki</creatorcontrib><description>Polycondensation of 1,2,4,5-tetrafluorobenzene (1) with 3,3′-dihexyl-2,2′-bithiophene via Pd/Ag dual-catalyzed cross-dehydrogenative coupling was examined. In situ deprotonation-metalation of 1 with Ag salt proceeded smoothly at 25 °C, and the subsequent transmetalation with a Pd catalyst provided a cross-coupling product. The sequential one-pot two-step reaction method effectively suppressed undesired homo-coupling defects during polymerization. The obtained highly regioregular polymer had a packing structure and exhibited strong fluorescence in the film state, which was also evaluated for use as an emitting material in organic light-emitting diodes.
[Display omitted]
•One-pot two-step cross-dehydrogenative-coupling polycondensation is demonstrated.•The sequential one-pot two-step reaction effectively suppressed undesired homo-coupling defects.•The regioregular polymer exhibits high crystallinity and strong fluorescence.</description><identifier>ISSN: 0379-6779</identifier><identifier>EISSN: 1879-3290</identifier><identifier>DOI: 10.1016/j.synthmet.2023.117279</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Conjugated polymers ; Cross-dehydrogenative-coupling reaction ; Emitting materials ; Pd/Ag dual-catalyst ; Polycondensation</subject><ispartof>Synthetic metals, 2023-03, Vol.293, p.117279, Article 117279</ispartof><rights>2023 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03</citedby><cites>FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Onda, Naoki</creatorcontrib><creatorcontrib>Sato, Ryota</creatorcontrib><creatorcontrib>Kuwabara, Junpei</creatorcontrib><creatorcontrib>Yasuda, Takeshi</creatorcontrib><creatorcontrib>Kanbara, Takaki</creatorcontrib><title>One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer</title><title>Synthetic metals</title><description>Polycondensation of 1,2,4,5-tetrafluorobenzene (1) with 3,3′-dihexyl-2,2′-bithiophene via Pd/Ag dual-catalyzed cross-dehydrogenative coupling was examined. In situ deprotonation-metalation of 1 with Ag salt proceeded smoothly at 25 °C, and the subsequent transmetalation with a Pd catalyst provided a cross-coupling product. The sequential one-pot two-step reaction method effectively suppressed undesired homo-coupling defects during polymerization. The obtained highly regioregular polymer had a packing structure and exhibited strong fluorescence in the film state, which was also evaluated for use as an emitting material in organic light-emitting diodes.
[Display omitted]
•One-pot two-step cross-dehydrogenative-coupling polycondensation is demonstrated.•The sequential one-pot two-step reaction effectively suppressed undesired homo-coupling defects.•The regioregular polymer exhibits high crystallinity and strong fluorescence.</description><subject>Conjugated polymers</subject><subject>Cross-dehydrogenative-coupling reaction</subject><subject>Emitting materials</subject><subject>Pd/Ag dual-catalyst</subject><subject>Polycondensation</subject><issn>0379-6779</issn><issn>1879-3290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkM1qwzAQhEVpoenPKxS9gF1Jtiz71hL6B4Fc2rOQ5FXi4EhGUlJc6LvXSdpzTzuwzOzsh9AdJTkltLrf5HF0ab2FlDPCipxSwURzhma0Fk1WsIacoxkpJl0J0Vyiqxg3hBDaMD5D30sH2eATTp8-iwkGbIKPMWthPbbBr8Cp1O0hM3439J1b4cH3o_GuBRenjXfY-oCPBSB2EXuLE6SgbL_zwWtwXzAd0CpCiyfbZrdSaZKHlC2EG3RhVR_h9ndeo4_np_f5a7ZYvrzNHxeZKXiVsoawSoESipe8rrkRQthaCEU55wQ0UFrrUlfAatKWldBEMzAlLVpmmQZLimtUnXKPzwWwcgjdVoVRUiIPEOVG_kGUB4jyBHEyPpyMMLXbdxBkNB04A20XwCTZ-u6_iB9mCIPG</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Onda, Naoki</creator><creator>Sato, Ryota</creator><creator>Kuwabara, Junpei</creator><creator>Yasuda, Takeshi</creator><creator>Kanbara, Takaki</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230301</creationdate><title>One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer</title><author>Onda, Naoki ; Sato, Ryota ; Kuwabara, Junpei ; Yasuda, Takeshi ; Kanbara, Takaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Conjugated polymers</topic><topic>Cross-dehydrogenative-coupling reaction</topic><topic>Emitting materials</topic><topic>Pd/Ag dual-catalyst</topic><topic>Polycondensation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Onda, Naoki</creatorcontrib><creatorcontrib>Sato, Ryota</creatorcontrib><creatorcontrib>Kuwabara, Junpei</creatorcontrib><creatorcontrib>Yasuda, Takeshi</creatorcontrib><creatorcontrib>Kanbara, Takaki</creatorcontrib><collection>CrossRef</collection><jtitle>Synthetic metals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Onda, Naoki</au><au>Sato, Ryota</au><au>Kuwabara, Junpei</au><au>Yasuda, Takeshi</au><au>Kanbara, Takaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer</atitle><jtitle>Synthetic metals</jtitle><date>2023-03-01</date><risdate>2023</risdate><volume>293</volume><spage>117279</spage><pages>117279-</pages><artnum>117279</artnum><issn>0379-6779</issn><eissn>1879-3290</eissn><abstract>Polycondensation of 1,2,4,5-tetrafluorobenzene (1) with 3,3′-dihexyl-2,2′-bithiophene via Pd/Ag dual-catalyzed cross-dehydrogenative coupling was examined. In situ deprotonation-metalation of 1 with Ag salt proceeded smoothly at 25 °C, and the subsequent transmetalation with a Pd catalyst provided a cross-coupling product. The sequential one-pot two-step reaction method effectively suppressed undesired homo-coupling defects during polymerization. The obtained highly regioregular polymer had a packing structure and exhibited strong fluorescence in the film state, which was also evaluated for use as an emitting material in organic light-emitting diodes.
[Display omitted]
•One-pot two-step cross-dehydrogenative-coupling polycondensation is demonstrated.•The sequential one-pot two-step reaction effectively suppressed undesired homo-coupling defects.•The regioregular polymer exhibits high crystallinity and strong fluorescence.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.synthmet.2023.117279</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0379-6779 |
ispartof | Synthetic metals, 2023-03, Vol.293, p.117279, Article 117279 |
issn | 0379-6779 1879-3290 |
language | eng |
recordid | cdi_crossref_primary_10_1016_j_synthmet_2023_117279 |
source | ScienceDirect Journals |
subjects | Conjugated polymers Cross-dehydrogenative-coupling reaction Emitting materials Pd/Ag dual-catalyst Polycondensation |
title | One-pot two-step cross-dehydrogenative-coupling polycondensation for synthesis of tetrafluorobenzene-based conjugated polymer |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A12%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=One-pot%20two-step%20cross-dehydrogenative-coupling%20polycondensation%20for%20synthesis%20of%20tetrafluorobenzene-based%20conjugated%20polymer&rft.jtitle=Synthetic%20metals&rft.au=Onda,%20Naoki&rft.date=2023-03-01&rft.volume=293&rft.spage=117279&rft.pages=117279-&rft.artnum=117279&rft.issn=0379-6779&rft.eissn=1879-3290&rft_id=info:doi/10.1016/j.synthmet.2023.117279&rft_dat=%3Celsevier_cross%3ES0379677923000012%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c356t-9026aea7a545885c777f877a15550ebe118b4b6e280d467b0b2ec413d2f2bef03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |