Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases

We report the synthesis and mesophase characterization of a series of novel di- and tetra-aryl acenequinones. Diphenyl-acenequinones 1 and 2 exhibit monotropic mesophases while tetra-aryl acenequinones 4 and 5 exhibit stable columnar hexagonal mesophases. Compound 4 exhibits a more stable columnar m...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:New journal of chemistry 2016, Vol.4 (7), p.5985-5988
Hauptverfasser: Paquette, Joseph A, Yardley, Rebecca E, Yu, Joanne Wing-Yan, Eichhorn, S. Holger, Maly, Kenneth E
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5988
container_issue 7
container_start_page 5985
container_title New journal of chemistry
container_volume 4
creator Paquette, Joseph A
Yardley, Rebecca E
Yu, Joanne Wing-Yan
Eichhorn, S. Holger
Maly, Kenneth E
description We report the synthesis and mesophase characterization of a series of novel di- and tetra-aryl acenequinones. Diphenyl-acenequinones 1 and 2 exhibit monotropic mesophases while tetra-aryl acenequinones 4 and 5 exhibit stable columnar hexagonal mesophases. Compound 4 exhibits a more stable columnar mesophase than 5 , consistent with a packing motif where molecules are stacked in perpendicular arrangement. The mesomorphic properties of novel acenequinones reveals that a perpendicular packing motif is an important factor for determining mesophase stability.
doi_str_mv 10.1039/c6nj00301j
format Article
fullrecord <record><control><sourceid>rsc_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1039_C6NJ00301J</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c6nj00301j</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-d5d7784919b4ca07bb4d71a0880eeac116ea8748d00f575201f02c02d268dc073</originalsourceid><addsrcrecordid>eNpFkEtLAzEUhYMoWKsb90LWwui980hm3JXiqxTd6HpIkxs6ZZqpSabgvzda0dW9h_NxFh9jlwg3CEVzq4XbABSAmyM2wUI0WZMLPE4_lmUGVSlO2VkIiUGUAicszFxce5Vx5QzfkYtKk6OPsXODI27Id3sVuz2FO94524_kNPHB8hD9qOPoU3A8ronbwW8TmVJq9dCPW6c877s0Zbj2nyGqnu_WKlA4ZydW9YEufu-UvT_cv82fsuXr4_N8tsx0gU3MTGWkrMsGm1WpFcjVqjQSFdQ1ECmNKEjVsqwNgK1klQNayDXkJhe10SCLKbs-7Go_hODJtjvfbZX_bBHab13tXLwsfnQtEnx1gH3Qf9y_zuILi5xpiQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Paquette, Joseph A ; Yardley, Rebecca E ; Yu, Joanne Wing-Yan ; Eichhorn, S. Holger ; Maly, Kenneth E</creator><creatorcontrib>Paquette, Joseph A ; Yardley, Rebecca E ; Yu, Joanne Wing-Yan ; Eichhorn, S. Holger ; Maly, Kenneth E</creatorcontrib><description>We report the synthesis and mesophase characterization of a series of novel di- and tetra-aryl acenequinones. Diphenyl-acenequinones 1 and 2 exhibit monotropic mesophases while tetra-aryl acenequinones 4 and 5 exhibit stable columnar hexagonal mesophases. Compound 4 exhibits a more stable columnar mesophase than 5 , consistent with a packing motif where molecules are stacked in perpendicular arrangement. The mesomorphic properties of novel acenequinones reveals that a perpendicular packing motif is an important factor for determining mesophase stability.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c6nj00301j</identifier><language>eng</language><ispartof>New journal of chemistry, 2016, Vol.4 (7), p.5985-5988</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-d5d7784919b4ca07bb4d71a0880eeac116ea8748d00f575201f02c02d268dc073</citedby><cites>FETCH-LOGICAL-c319t-d5d7784919b4ca07bb4d71a0880eeac116ea8748d00f575201f02c02d268dc073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>Paquette, Joseph A</creatorcontrib><creatorcontrib>Yardley, Rebecca E</creatorcontrib><creatorcontrib>Yu, Joanne Wing-Yan</creatorcontrib><creatorcontrib>Eichhorn, S. Holger</creatorcontrib><creatorcontrib>Maly, Kenneth E</creatorcontrib><title>Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases</title><title>New journal of chemistry</title><description>We report the synthesis and mesophase characterization of a series of novel di- and tetra-aryl acenequinones. Diphenyl-acenequinones 1 and 2 exhibit monotropic mesophases while tetra-aryl acenequinones 4 and 5 exhibit stable columnar hexagonal mesophases. Compound 4 exhibits a more stable columnar mesophase than 5 , consistent with a packing motif where molecules are stacked in perpendicular arrangement. The mesomorphic properties of novel acenequinones reveals that a perpendicular packing motif is an important factor for determining mesophase stability.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLAzEUhYMoWKsb90LWwui980hm3JXiqxTd6HpIkxs6ZZqpSabgvzda0dW9h_NxFh9jlwg3CEVzq4XbABSAmyM2wUI0WZMLPE4_lmUGVSlO2VkIiUGUAicszFxce5Vx5QzfkYtKk6OPsXODI27Id3sVuz2FO94524_kNPHB8hD9qOPoU3A8ronbwW8TmVJq9dCPW6c877s0Zbj2nyGqnu_WKlA4ZydW9YEufu-UvT_cv82fsuXr4_N8tsx0gU3MTGWkrMsGm1WpFcjVqjQSFdQ1ECmNKEjVsqwNgK1klQNayDXkJhe10SCLKbs-7Go_hODJtjvfbZX_bBHab13tXLwsfnQtEnx1gH3Qf9y_zuILi5xpiQ</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Paquette, Joseph A</creator><creator>Yardley, Rebecca E</creator><creator>Yu, Joanne Wing-Yan</creator><creator>Eichhorn, S. Holger</creator><creator>Maly, Kenneth E</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2016</creationdate><title>Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases</title><author>Paquette, Joseph A ; Yardley, Rebecca E ; Yu, Joanne Wing-Yan ; Eichhorn, S. Holger ; Maly, Kenneth E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-d5d7784919b4ca07bb4d71a0880eeac116ea8748d00f575201f02c02d268dc073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paquette, Joseph A</creatorcontrib><creatorcontrib>Yardley, Rebecca E</creatorcontrib><creatorcontrib>Yu, Joanne Wing-Yan</creatorcontrib><creatorcontrib>Eichhorn, S. Holger</creatorcontrib><creatorcontrib>Maly, Kenneth E</creatorcontrib><collection>CrossRef</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paquette, Joseph A</au><au>Yardley, Rebecca E</au><au>Yu, Joanne Wing-Yan</au><au>Eichhorn, S. Holger</au><au>Maly, Kenneth E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases</atitle><jtitle>New journal of chemistry</jtitle><date>2016</date><risdate>2016</risdate><volume>4</volume><issue>7</issue><spage>5985</spage><epage>5988</epage><pages>5985-5988</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>We report the synthesis and mesophase characterization of a series of novel di- and tetra-aryl acenequinones. Diphenyl-acenequinones 1 and 2 exhibit monotropic mesophases while tetra-aryl acenequinones 4 and 5 exhibit stable columnar hexagonal mesophases. Compound 4 exhibits a more stable columnar mesophase than 5 , consistent with a packing motif where molecules are stacked in perpendicular arrangement. The mesomorphic properties of novel acenequinones reveals that a perpendicular packing motif is an important factor for determining mesophase stability.</abstract><doi>10.1039/c6nj00301j</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1144-0546
ispartof New journal of chemistry, 2016, Vol.4 (7), p.5985-5988
issn 1144-0546
1369-9261
language eng
recordid cdi_crossref_primary_10_1039_C6NJ00301J
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Anthra- and pentacenequinone derivatives: influence of structure on the formation of columnar liquid crystal phases
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T21%3A25%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anthra-%20and%20pentacenequinone%20derivatives:%20influence%20of%20structure%20on%20the%20formation%20of%20columnar%20liquid%20crystal%20phases&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Paquette,%20Joseph%20A&rft.date=2016&rft.volume=4&rft.issue=7&rft.spage=5985&rft.epage=5988&rft.pages=5985-5988&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/c6nj00301j&rft_dat=%3Crsc_cross%3Ec6nj00301j%3C/rsc_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true