Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids

A series of fluorene-based grid molecules (so-called Grid fluorenes) have been synthesized by means of shape-supported cyclization, starting from H-shaped precursors via the alternative Friedel–Crafts reactions of fluorenols and Suzuki cross-coupling reactions with key cyclization yields up to 26%....

Full description

Saved in:
Bibliographic Details
Published in:Organic letters 2014-03, Vol.16 (6), p.1748-1751
Main Authors: Wang, Long, Zhang, Guang-Wei, Ou, Chang-Jin, Xie, Ling-Hai, Lin, Jin-Yi, Liu, Yu-Yu, Huang, Wei
Format: Article
Language:English
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-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413
cites cdi_FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413
container_end_page 1751
container_issue 6
container_start_page 1748
container_title Organic letters
container_volume 16
creator Wang, Long
Zhang, Guang-Wei
Ou, Chang-Jin
Xie, Ling-Hai
Lin, Jin-Yi
Liu, Yu-Yu
Huang, Wei
description A series of fluorene-based grid molecules (so-called Grid fluorenes) have been synthesized by means of shape-supported cyclization, starting from H-shaped precursors via the alternative Friedel–Crafts reactions of fluorenols and Suzuki cross-coupling reactions with key cyclization yields up to 26%. Fluorenol approaches and nanogrids open a door to soluble one-, two-, or three-dimensional nanoporous polymers as next-generation polymer mechano-semiconductors facing a new era of consciousness.
doi_str_mv 10.1021/ol500439z
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1509408396</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1509408396</sourcerecordid><originalsourceid>FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413</originalsourceid><addsrcrecordid>eNptkLFOwzAQhi0EoqUw8ALICxIMAduxk3ikFQWkig6FDSly7EtJlcTFjocy8Q68IU9CUKET0_06ffp19yF0SskVJYxe21oQwmP5voeGVLA4Solg-7uckAE68n5FCO038hANGE8ozTgdopepq8BA_fXxOXGq7Dwe266zTRTWeLFpu1fwlce2xNM6WActRGPlweCFrUNRA56FpmrBa2g7PHdL1VYaP6rWLl1l_DE6KFXt4eR3jtDz9PZpch_N5ncPk5tZpGIqukgaWRQyFUooTTKTFYRkKTBtNOW80AAgDeNZkkquY53FSZZoIQgzWhvFOI1H6GLbu3b2LYDv8qbqT6pr1YINPqeCSE6yWCY9erlFtbPeOyjztasa5TY5JfmPzHwns2fPfmtD0YDZkX_2euB8Cyjt85UNru2__KfoGw7rfNw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1509408396</pqid></control><display><type>article</type><title>Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Wang, Long ; Zhang, Guang-Wei ; Ou, Chang-Jin ; Xie, Ling-Hai ; Lin, Jin-Yi ; Liu, Yu-Yu ; Huang, Wei</creator><creatorcontrib>Wang, Long ; Zhang, Guang-Wei ; Ou, Chang-Jin ; Xie, Ling-Hai ; Lin, Jin-Yi ; Liu, Yu-Yu ; Huang, Wei</creatorcontrib><description>A series of fluorene-based grid molecules (so-called Grid fluorenes) have been synthesized by means of shape-supported cyclization, starting from H-shaped precursors via the alternative Friedel–Crafts reactions of fluorenols and Suzuki cross-coupling reactions with key cyclization yields up to 26%. Fluorenol approaches and nanogrids open a door to soluble one-, two-, or three-dimensional nanoporous polymers as next-generation polymer mechano-semiconductors facing a new era of consciousness.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol500439z</identifier><identifier>PMID: 24611841</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Organic letters, 2014-03, Vol.16 (6), p.1748-1751</ispartof><rights>Copyright © 2014 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413</citedby><cites>FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24611841$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Long</creatorcontrib><creatorcontrib>Zhang, Guang-Wei</creatorcontrib><creatorcontrib>Ou, Chang-Jin</creatorcontrib><creatorcontrib>Xie, Ling-Hai</creatorcontrib><creatorcontrib>Lin, Jin-Yi</creatorcontrib><creatorcontrib>Liu, Yu-Yu</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><title>Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>A series of fluorene-based grid molecules (so-called Grid fluorenes) have been synthesized by means of shape-supported cyclization, starting from H-shaped precursors via the alternative Friedel–Crafts reactions of fluorenols and Suzuki cross-coupling reactions with key cyclization yields up to 26%. Fluorenol approaches and nanogrids open a door to soluble one-, two-, or three-dimensional nanoporous polymers as next-generation polymer mechano-semiconductors facing a new era of consciousness.</description><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNptkLFOwzAQhi0EoqUw8ALICxIMAduxk3ikFQWkig6FDSly7EtJlcTFjocy8Q68IU9CUKET0_06ffp19yF0SskVJYxe21oQwmP5voeGVLA4Solg-7uckAE68n5FCO038hANGE8ozTgdopepq8BA_fXxOXGq7Dwe266zTRTWeLFpu1fwlce2xNM6WActRGPlweCFrUNRA56FpmrBa2g7PHdL1VYaP6rWLl1l_DE6KFXt4eR3jtDz9PZpch_N5ncPk5tZpGIqukgaWRQyFUooTTKTFYRkKTBtNOW80AAgDeNZkkquY53FSZZoIQgzWhvFOI1H6GLbu3b2LYDv8qbqT6pr1YINPqeCSE6yWCY9erlFtbPeOyjztasa5TY5JfmPzHwns2fPfmtD0YDZkX_2euB8Cyjt85UNru2__KfoGw7rfNw</recordid><startdate>20140321</startdate><enddate>20140321</enddate><creator>Wang, Long</creator><creator>Zhang, Guang-Wei</creator><creator>Ou, Chang-Jin</creator><creator>Xie, Ling-Hai</creator><creator>Lin, Jin-Yi</creator><creator>Liu, Yu-Yu</creator><creator>Huang, Wei</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140321</creationdate><title>Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids</title><author>Wang, Long ; Zhang, Guang-Wei ; Ou, Chang-Jin ; Xie, Ling-Hai ; Lin, Jin-Yi ; Liu, Yu-Yu ; Huang, Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Long</creatorcontrib><creatorcontrib>Zhang, Guang-Wei</creatorcontrib><creatorcontrib>Ou, Chang-Jin</creatorcontrib><creatorcontrib>Xie, Ling-Hai</creatorcontrib><creatorcontrib>Lin, Jin-Yi</creatorcontrib><creatorcontrib>Liu, Yu-Yu</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Long</au><au>Zhang, Guang-Wei</au><au>Ou, Chang-Jin</au><au>Xie, Ling-Hai</au><au>Lin, Jin-Yi</au><au>Liu, Yu-Yu</au><au>Huang, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2014-03-21</date><risdate>2014</risdate><volume>16</volume><issue>6</issue><spage>1748</spage><epage>1751</epage><pages>1748-1751</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>A series of fluorene-based grid molecules (so-called Grid fluorenes) have been synthesized by means of shape-supported cyclization, starting from H-shaped precursors via the alternative Friedel–Crafts reactions of fluorenols and Suzuki cross-coupling reactions with key cyclization yields up to 26%. Fluorenol approaches and nanogrids open a door to soluble one-, two-, or three-dimensional nanoporous polymers as next-generation polymer mechano-semiconductors facing a new era of consciousness.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24611841</pmid><doi>10.1021/ol500439z</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1523-7060
ispartof Organic letters, 2014-03, Vol.16 (6), p.1748-1751
issn 1523-7060
1523-7052
language eng
recordid cdi_proquest_miscellaneous_1509408396
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Friedel–Crafts Bottom-up Synthesis of Fluorene-Based Soluble Luminescent Organic Nanogrids
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T21%3A22%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Friedel%E2%80%93Crafts%20Bottom-up%20Synthesis%20of%20Fluorene-Based%20Soluble%20Luminescent%20Organic%20Nanogrids&rft.jtitle=Organic%20letters&rft.au=Wang,%20Long&rft.date=2014-03-21&rft.volume=16&rft.issue=6&rft.spage=1748&rft.epage=1751&rft.pages=1748-1751&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol500439z&rft_dat=%3Cproquest_cross%3E1509408396%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a315t-9d9bb975a5ac08d8b0087e2cdc144bceee9d2486794c3c83686c5502dccda2413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1509408396&rft_id=info:pmid/24611841&rfr_iscdi=true