Effect of the different rigidity of the chiral crosslinker on phase behaviors of side-chain chiral liquid crystalline elastomers
In the present work, the phase behaviors of two series of side-chain liquid crystalline elastomers (PI and PII series) derived from the same nematic liquid crystalline monomer and the different rigidity of chiral bisolefinic crosslinking units have been compared and studied extensively, and the effe...
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Veröffentlicht in: | Journal of applied polymer science 2008-02, Vol.107 (3), p.1479-1486 |
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description | In the present work, the phase behaviors of two series of side-chain liquid crystalline elastomers (PI and PII series) derived from the same nematic liquid crystalline monomer and the different rigidity of chiral bisolefinic crosslinking units have been compared and studied extensively, and the effect of the different rigidity of crosslinker on the phase behavior of elastomers has been discussed. The chemical structure of the monomers and polymers obtained were confirmed by FTIR and ¹H NMR spectroscopy. The phase behaviors were investigated by differential scanning calorimetry, polarizing optical microscopy measurement, thermogravimetric analyses, and X-ray diffraction measurement. The two series of elastomers showed smectic or cholesteric phases. When the amount of different crosslinking units was less than 15 mol %, both of the elastomers displayed elasticity, reversible phase transition with wide mesophase temperature ranges, and high thermal stability. It is shown that the isotropization temperature values of PII series are higher than those of PI series, and the glass transition temperature values of PII series varied smoothly and that of PI series changed smoothly first and then abruptly with increasing the contents of crosslinkers with different rigidity. In addition, PI series showed an interesting change in LC texture near clearing point, but PII series did not. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 |
doi_str_mv | 10.1002/app.27059 |
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The chemical structure of the monomers and polymers obtained were confirmed by FTIR and ¹H NMR spectroscopy. The phase behaviors were investigated by differential scanning calorimetry, polarizing optical microscopy measurement, thermogravimetric analyses, and X-ray diffraction measurement. The two series of elastomers showed smectic or cholesteric phases. When the amount of different crosslinking units was less than 15 mol %, both of the elastomers displayed elasticity, reversible phase transition with wide mesophase temperature ranges, and high thermal stability. It is shown that the isotropization temperature values of PII series are higher than those of PI series, and the glass transition temperature values of PII series varied smoothly and that of PI series changed smoothly first and then abruptly with increasing the contents of crosslinkers with different rigidity. In addition, PI series showed an interesting change in LC texture near clearing point, but PII series did not. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.27059</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; Chemical modifications ; chiral smectic C ; crosslinking ; elastomer ; Exact sciences and technology ; Inorganic and organomineral polymers ; liquid crystal ; Physicochemistry of polymers</subject><ispartof>Journal of applied polymer science, 2008-02, Vol.107 (3), p.1479-1486</ispartof><rights>Copyright © 2007 Wiley Periodicals, Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3929-b7ed0563f679fde155a7e25c75511f47d15767aca7334708fe87ff9c604a0cec3</citedby><cites>FETCH-LOGICAL-c3929-b7ed0563f679fde155a7e25c75511f47d15767aca7334708fe87ff9c604a0cec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fapp.27059$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.27059$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19961536$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Bao-Yan</creatorcontrib><creatorcontrib>He, Xiao-Zhi</creatorcontrib><creatorcontrib>Liao, Qing-Feng</creatorcontrib><creatorcontrib>Zhou, Qun-Hua</creatorcontrib><title>Effect of the different rigidity of the chiral crosslinker on phase behaviors of side-chain chiral liquid crystalline elastomers</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>In the present work, the phase behaviors of two series of side-chain liquid crystalline elastomers (PI and PII series) derived from the same nematic liquid crystalline monomer and the different rigidity of chiral bisolefinic crosslinking units have been compared and studied extensively, and the effect of the different rigidity of crosslinker on the phase behavior of elastomers has been discussed. The chemical structure of the monomers and polymers obtained were confirmed by FTIR and ¹H NMR spectroscopy. The phase behaviors were investigated by differential scanning calorimetry, polarizing optical microscopy measurement, thermogravimetric analyses, and X-ray diffraction measurement. The two series of elastomers showed smectic or cholesteric phases. When the amount of different crosslinking units was less than 15 mol %, both of the elastomers displayed elasticity, reversible phase transition with wide mesophase temperature ranges, and high thermal stability. It is shown that the isotropization temperature values of PII series are higher than those of PI series, and the glass transition temperature values of PII series varied smoothly and that of PI series changed smoothly first and then abruptly with increasing the contents of crosslinkers with different rigidity. In addition, PI series showed an interesting change in LC texture near clearing point, but PII series did not. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008</description><subject>Applied sciences</subject><subject>Chemical modifications</subject><subject>chiral smectic C</subject><subject>crosslinking</subject><subject>elastomer</subject><subject>Exact sciences and technology</subject><subject>Inorganic and organomineral polymers</subject><subject>liquid crystal</subject><subject>Physicochemistry of polymers</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kMFO3DAQhqOqSN1CD32C-tJKPQTsOLbjIwIKSCuK1AJHa3DGxMWbBDvbdm99dAxh21NPI2u-79f4L4r3jO4zSqsDGMf9SlGhXxULRrUqa1k1r4tF3rGy0Vq8Kd6m9INSxgSVi-LPiXNoJzI4MnVIWp-fEfuJRH_nWz9tthvb-QiB2DikFHx_j5EMPRk7SEhusYOffojpCU6-xdJ24PutE_zD2rdZ3aQJQpaRYIA0DSuMaa_YcRASvnuZu8XVl5PvR2fl8uvp-dHhsrRcV7q8VdhSIbmTSrsWmRCgsBJWCcGYq1XLhJIKLCjOa0Ubh41yTltJa6AWLd8tPs25Yxwe1pgms_LJYgjQ47BOhjPW1LphGfw8g89fjejMGP0K4sYwap46Nrlj89xxZj--hEKyEFyE3vr0T9BaMsFl5g5m7pcPuPl_oDm8vNwml7Ph04S__xoQ741UXAlzc3FqhDxWF9dnlVlm_sPMOxgM3MV8xdW3ijJOacNrVjf8EeU2pSo</recordid><startdate>20080205</startdate><enddate>20080205</enddate><creator>Zhang, Bao-Yan</creator><creator>He, Xiao-Zhi</creator><creator>Liao, Qing-Feng</creator><creator>Zhou, Qun-Hua</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20080205</creationdate><title>Effect of the different rigidity of the chiral crosslinker on phase behaviors of side-chain chiral liquid crystalline elastomers</title><author>Zhang, Bao-Yan ; He, Xiao-Zhi ; Liao, Qing-Feng ; Zhou, Qun-Hua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3929-b7ed0563f679fde155a7e25c75511f47d15767aca7334708fe87ff9c604a0cec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Applied sciences</topic><topic>Chemical modifications</topic><topic>chiral smectic C</topic><topic>crosslinking</topic><topic>elastomer</topic><topic>Exact sciences and technology</topic><topic>Inorganic and organomineral polymers</topic><topic>liquid crystal</topic><topic>Physicochemistry of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Bao-Yan</creatorcontrib><creatorcontrib>He, Xiao-Zhi</creatorcontrib><creatorcontrib>Liao, Qing-Feng</creatorcontrib><creatorcontrib>Zhou, Qun-Hua</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Bao-Yan</au><au>He, Xiao-Zhi</au><au>Liao, Qing-Feng</au><au>Zhou, Qun-Hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of the different rigidity of the chiral crosslinker on phase behaviors of side-chain chiral liquid crystalline elastomers</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2008-02-05</date><risdate>2008</risdate><volume>107</volume><issue>3</issue><spage>1479</spage><epage>1486</epage><pages>1479-1486</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>In the present work, the phase behaviors of two series of side-chain liquid crystalline elastomers (PI and PII series) derived from the same nematic liquid crystalline monomer and the different rigidity of chiral bisolefinic crosslinking units have been compared and studied extensively, and the effect of the different rigidity of crosslinker on the phase behavior of elastomers has been discussed. The chemical structure of the monomers and polymers obtained were confirmed by FTIR and ¹H NMR spectroscopy. The phase behaviors were investigated by differential scanning calorimetry, polarizing optical microscopy measurement, thermogravimetric analyses, and X-ray diffraction measurement. The two series of elastomers showed smectic or cholesteric phases. When the amount of different crosslinking units was less than 15 mol %, both of the elastomers displayed elasticity, reversible phase transition with wide mesophase temperature ranges, and high thermal stability. It is shown that the isotropization temperature values of PII series are higher than those of PI series, and the glass transition temperature values of PII series varied smoothly and that of PI series changed smoothly first and then abruptly with increasing the contents of crosslinkers with different rigidity. In addition, PI series showed an interesting change in LC texture near clearing point, but PII series did not. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.27059</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Chemical modifications chiral smectic C crosslinking elastomer Exact sciences and technology Inorganic and organomineral polymers liquid crystal Physicochemistry of polymers |
title | Effect of the different rigidity of the chiral crosslinker on phase behaviors of side-chain chiral liquid crystalline elastomers |
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