Loading…

Facile access to benzofuran-based bis-stilbene for organic laser dyes

A concise and efficient synthetic protocol for the synthesis of furan-based bis-stilbene derivatives (BPBFCz1) was described, which is a very promising organic laser dye. Starting with 4,4'-diethynylbiphenyl, BPBFCz1 was prepared with a total yield of 40% through a three-step classical reaction...

Full description

Saved in:
Bibliographic Details
Published in:Synthetic communications 2024-06, Vol.54 (11), p.927-934
Main Authors: Zheng, Ziyi, Bian, Guangling, Song, Ling
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c286t-149b644f2cce2d1be6bbca1ab8cad0a6bf634833f23cce400047466760cc4e0c3
container_end_page 934
container_issue 11
container_start_page 927
container_title Synthetic communications
container_volume 54
creator Zheng, Ziyi
Bian, Guangling
Song, Ling
description A concise and efficient synthetic protocol for the synthesis of furan-based bis-stilbene derivatives (BPBFCz1) was described, which is a very promising organic laser dye. Starting with 4,4'-diethynylbiphenyl, BPBFCz1 was prepared with a total yield of 40% through a three-step classical reaction of Sonogashira Coupling, intramolecular cyclization of 2-alkynyl phenol, and Buchwald Hartwig cross-coupling. The crystal structure of BPBFCz1 was presented for the first time. The synthesis strategy was applied to the synthesis of other three materials with similar structure and the yields of 28.6-36.6% were obtained.
doi_str_mv 10.1080/00397911.2024.2356632
format article
fullrecord <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_proquest_journals_3062327142</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3062327142</sourcerecordid><originalsourceid>FETCH-LOGICAL-c286t-149b644f2cce2d1be6bbca1ab8cad0a6bf634833f23cce400047466760cc4e0c3</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMoWKs_QQh4Tp18bHb3ppRWhYIXPYckm0jKdlOTLVJ_vVmqV09zmOedl3kQuqWwoNDAPQBv65bSBQMmFoxXUnJ2hma04owwwdk5mk0MmaBLdJXzFoBWddPO0Gqtbegd1ta6nPEYsXHDd_SHpAdidHYdNiGTPIa-LBz2MeGYPvQQLO7LOuHu6PI1uvC6z-7md87R-3r1tnwmm9enl-XjhljWyJFQ0RophGeljHXUOGmM1VSbxuoOtDRectFw7hkvhAAAUQspawnWCgeWz9Hd6e4-xc-Dy6PaxkMaSqXiIBlnNRWsUNWJsinmnJxX-xR2Oh0VBTUZU3_G1GRM_RoruYdTLgzlzZ3-iqnv1KiPfUy--LCh1Px_4gcpAHH7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3062327142</pqid></control><display><type>article</type><title>Facile access to benzofuran-based bis-stilbene for organic laser dyes</title><source>Taylor and Francis Science and Technology Collection</source><creator>Zheng, Ziyi ; Bian, Guangling ; Song, Ling</creator><creatorcontrib>Zheng, Ziyi ; Bian, Guangling ; Song, Ling</creatorcontrib><description>A concise and efficient synthetic protocol for the synthesis of furan-based bis-stilbene derivatives (BPBFCz1) was described, which is a very promising organic laser dye. Starting with 4,4'-diethynylbiphenyl, BPBFCz1 was prepared with a total yield of 40% through a three-step classical reaction of Sonogashira Coupling, intramolecular cyclization of 2-alkynyl phenol, and Buchwald Hartwig cross-coupling. The crystal structure of BPBFCz1 was presented for the first time. The synthesis strategy was applied to the synthesis of other three materials with similar structure and the yields of 28.6-36.6% were obtained.</description><identifier>ISSN: 0039-7911</identifier><identifier>EISSN: 1532-2432</identifier><identifier>DOI: 10.1080/00397911.2024.2356632</identifier><language>eng</language><publisher>Philadelphia: Taylor &amp; Francis</publisher><subject>benzofuran ; bis-stilbene ; Cross coupling ; Crystal structure ; Dyes ; organic gain media ; Organic laser dyes ; Organic lasers ; sonogashira coupling ; Stilbene ; Synthesis</subject><ispartof>Synthetic communications, 2024-06, Vol.54 (11), p.927-934</ispartof><rights>2024 Taylor &amp; Francis Group, LLC 2024</rights><rights>2024 Taylor &amp; Francis Group, LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c286t-149b644f2cce2d1be6bbca1ab8cad0a6bf634833f23cce400047466760cc4e0c3</cites><orcidid>0000-0001-5824-7418 ; 0000-0003-0303-046X</orcidid></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>Zheng, Ziyi</creatorcontrib><creatorcontrib>Bian, Guangling</creatorcontrib><creatorcontrib>Song, Ling</creatorcontrib><title>Facile access to benzofuran-based bis-stilbene for organic laser dyes</title><title>Synthetic communications</title><description>A concise and efficient synthetic protocol for the synthesis of furan-based bis-stilbene derivatives (BPBFCz1) was described, which is a very promising organic laser dye. Starting with 4,4'-diethynylbiphenyl, BPBFCz1 was prepared with a total yield of 40% through a three-step classical reaction of Sonogashira Coupling, intramolecular cyclization of 2-alkynyl phenol, and Buchwald Hartwig cross-coupling. The crystal structure of BPBFCz1 was presented for the first time. The synthesis strategy was applied to the synthesis of other three materials with similar structure and the yields of 28.6-36.6% were obtained.</description><subject>benzofuran</subject><subject>bis-stilbene</subject><subject>Cross coupling</subject><subject>Crystal structure</subject><subject>Dyes</subject><subject>organic gain media</subject><subject>Organic laser dyes</subject><subject>Organic lasers</subject><subject>sonogashira coupling</subject><subject>Stilbene</subject><subject>Synthesis</subject><issn>0039-7911</issn><issn>1532-2432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWKs_QQh4Tp18bHb3ppRWhYIXPYckm0jKdlOTLVJ_vVmqV09zmOedl3kQuqWwoNDAPQBv65bSBQMmFoxXUnJ2hma04owwwdk5mk0MmaBLdJXzFoBWddPO0Gqtbegd1ta6nPEYsXHDd_SHpAdidHYdNiGTPIa-LBz2MeGYPvQQLO7LOuHu6PI1uvC6z-7md87R-3r1tnwmm9enl-XjhljWyJFQ0RophGeljHXUOGmM1VSbxuoOtDRectFw7hkvhAAAUQspawnWCgeWz9Hd6e4-xc-Dy6PaxkMaSqXiIBlnNRWsUNWJsinmnJxX-xR2Oh0VBTUZU3_G1GRM_RoruYdTLgzlzZ3-iqnv1KiPfUy--LCh1Px_4gcpAHH7</recordid><startdate>20240602</startdate><enddate>20240602</enddate><creator>Zheng, Ziyi</creator><creator>Bian, Guangling</creator><creator>Song, Ling</creator><general>Taylor &amp; Francis</general><general>Taylor &amp; Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-5824-7418</orcidid><orcidid>https://orcid.org/0000-0003-0303-046X</orcidid></search><sort><creationdate>20240602</creationdate><title>Facile access to benzofuran-based bis-stilbene for organic laser dyes</title><author>Zheng, Ziyi ; Bian, Guangling ; Song, Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-149b644f2cce2d1be6bbca1ab8cad0a6bf634833f23cce400047466760cc4e0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>benzofuran</topic><topic>bis-stilbene</topic><topic>Cross coupling</topic><topic>Crystal structure</topic><topic>Dyes</topic><topic>organic gain media</topic><topic>Organic laser dyes</topic><topic>Organic lasers</topic><topic>sonogashira coupling</topic><topic>Stilbene</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Ziyi</creatorcontrib><creatorcontrib>Bian, Guangling</creatorcontrib><creatorcontrib>Song, Ling</creatorcontrib><collection>CrossRef</collection><jtitle>Synthetic communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Ziyi</au><au>Bian, Guangling</au><au>Song, Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Facile access to benzofuran-based bis-stilbene for organic laser dyes</atitle><jtitle>Synthetic communications</jtitle><date>2024-06-02</date><risdate>2024</risdate><volume>54</volume><issue>11</issue><spage>927</spage><epage>934</epage><pages>927-934</pages><issn>0039-7911</issn><eissn>1532-2432</eissn><abstract>A concise and efficient synthetic protocol for the synthesis of furan-based bis-stilbene derivatives (BPBFCz1) was described, which is a very promising organic laser dye. Starting with 4,4'-diethynylbiphenyl, BPBFCz1 was prepared with a total yield of 40% through a three-step classical reaction of Sonogashira Coupling, intramolecular cyclization of 2-alkynyl phenol, and Buchwald Hartwig cross-coupling. The crystal structure of BPBFCz1 was presented for the first time. The synthesis strategy was applied to the synthesis of other three materials with similar structure and the yields of 28.6-36.6% were obtained.</abstract><cop>Philadelphia</cop><pub>Taylor &amp; Francis</pub><doi>10.1080/00397911.2024.2356632</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5824-7418</orcidid><orcidid>https://orcid.org/0000-0003-0303-046X</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0039-7911
ispartof Synthetic communications, 2024-06, Vol.54 (11), p.927-934
issn 0039-7911
1532-2432
language eng
recordid cdi_proquest_journals_3062327142
source Taylor and Francis Science and Technology Collection
subjects benzofuran
bis-stilbene
Cross coupling
Crystal structure
Dyes
organic gain media
Organic laser dyes
Organic lasers
sonogashira coupling
Stilbene
Synthesis
title Facile access to benzofuran-based bis-stilbene for organic laser dyes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T02%3A10%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Facile%20access%20to%20benzofuran-based%20bis-stilbene%20for%20organic%20laser%20dyes&rft.jtitle=Synthetic%20communications&rft.au=Zheng,%20Ziyi&rft.date=2024-06-02&rft.volume=54&rft.issue=11&rft.spage=927&rft.epage=934&rft.pages=927-934&rft.issn=0039-7911&rft.eissn=1532-2432&rft_id=info:doi/10.1080/00397911.2024.2356632&rft_dat=%3Cproquest_infor%3E3062327142%3C/proquest_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c286t-149b644f2cce2d1be6bbca1ab8cad0a6bf634833f23cce400047466760cc4e0c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3062327142&rft_id=info:pmid/&rfr_iscdi=true