Supramolecular Side-Chain Liquid Crystalline Polymers with Various Kinked Pendant Groups
Supramolecular side-chain liquid crystalline polymers with various kinked pendant groups are constructed from positional isomers of proton acceptor monomers and donor polymers (with different molecular weights) through hydrogen bonding. Monomer−monomer complexes of similar structures are built to co...
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Veröffentlicht in: | Macromolecules 1998-10, Vol.31 (21), p.7298-7311 |
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container_title | Macromolecules |
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creator | Lin, Hong-Cheu Lin, Yen-Shyi Lin, Yu-Sheng Chen, Yao-Te Chao, Ito Li, Ta-Wei |
description | Supramolecular side-chain liquid crystalline polymers with various kinked pendant groups are constructed from positional isomers of proton acceptor monomers and donor polymers (with different molecular weights) through hydrogen bonding. Monomer−monomer complexes of similar structures are built to compare the influence of the proton donors bound to the polymer backbones. Due to the bending effects introduced by the positional isomers, we are able to tune the molecular shape and thus to modify the mesogenic properties. New liquid crystalline properties are introduced by the kinked molecular geometry, and their kinked architecture is supported by the quantum mechanical calculations, the powder X-ray diffraction (XRD) patterns, and the deviation temperatures (ΔT). Mesogenic properties of monomer−polymer complexes have similar trends as those of monomer−monomer complexes. Compared with analogous hydrogen-bonded (H-bonded) monomer−monomer complexes, higher isotropization temperatures and broader ranges of mesogenic phases (e.g., SA phase) are observed in the kinked supramolecular polymers. Significantly, H-bonded positional isomerism leads to dissimilar structures and properties of supramolecular side-chain liquid crystalline polymers. |
doi_str_mv | 10.1021/ma980720e |
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Monomer−monomer complexes of similar structures are built to compare the influence of the proton donors bound to the polymer backbones. Due to the bending effects introduced by the positional isomers, we are able to tune the molecular shape and thus to modify the mesogenic properties. New liquid crystalline properties are introduced by the kinked molecular geometry, and their kinked architecture is supported by the quantum mechanical calculations, the powder X-ray diffraction (XRD) patterns, and the deviation temperatures (ΔT). Mesogenic properties of monomer−polymer complexes have similar trends as those of monomer−monomer complexes. Compared with analogous hydrogen-bonded (H-bonded) monomer−monomer complexes, higher isotropization temperatures and broader ranges of mesogenic phases (e.g., SA phase) are observed in the kinked supramolecular polymers. Significantly, H-bonded positional isomerism leads to dissimilar structures and properties of supramolecular side-chain liquid crystalline polymers.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma980720e</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Chemical modifications ; Exact sciences and technology ; Inorganic and organomineral polymers ; Physicochemistry of polymers</subject><ispartof>Macromolecules, 1998-10, Vol.31 (21), p.7298-7311</ispartof><rights>Copyright © 1998 American Chemical Society</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-8e3699041762e5dd03c14871363a024066d0dcd88937970ce2042bfe28621d8a3</citedby><cites>FETCH-LOGICAL-a324t-8e3699041762e5dd03c14871363a024066d0dcd88937970ce2042bfe28621d8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma980720e$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma980720e$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2438144$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Hong-Cheu</creatorcontrib><creatorcontrib>Lin, Yen-Shyi</creatorcontrib><creatorcontrib>Lin, Yu-Sheng</creatorcontrib><creatorcontrib>Chen, Yao-Te</creatorcontrib><creatorcontrib>Chao, Ito</creatorcontrib><creatorcontrib>Li, Ta-Wei</creatorcontrib><title>Supramolecular Side-Chain Liquid Crystalline Polymers with Various Kinked Pendant Groups</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Supramolecular side-chain liquid crystalline polymers with various kinked pendant groups are constructed from positional isomers of proton acceptor monomers and donor polymers (with different molecular weights) through hydrogen bonding. Monomer−monomer complexes of similar structures are built to compare the influence of the proton donors bound to the polymer backbones. Due to the bending effects introduced by the positional isomers, we are able to tune the molecular shape and thus to modify the mesogenic properties. New liquid crystalline properties are introduced by the kinked molecular geometry, and their kinked architecture is supported by the quantum mechanical calculations, the powder X-ray diffraction (XRD) patterns, and the deviation temperatures (ΔT). Mesogenic properties of monomer−polymer complexes have similar trends as those of monomer−monomer complexes. Compared with analogous hydrogen-bonded (H-bonded) monomer−monomer complexes, higher isotropization temperatures and broader ranges of mesogenic phases (e.g., SA phase) are observed in the kinked supramolecular polymers. Significantly, H-bonded positional isomerism leads to dissimilar structures and properties of supramolecular side-chain liquid crystalline polymers.</description><subject>Applied sciences</subject><subject>Chemical modifications</subject><subject>Exact sciences and technology</subject><subject>Inorganic and organomineral polymers</subject><subject>Physicochemistry of polymers</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpt0DtPwzAQAGALgUQpDPwDDzAwBPxK4owoogW1QKsWxGYdsaO65IWdCPrvCQrqxHTDffdE6JySa0oYvSkhkSRmxBygEQ0ZCULJw0M0IoSJIGFJfIxOvN8SQmko-Ai9rbrGQVkXJusKcHhltQnSDdgKz-1nZzVO3c63UBS2MnhRF7vSOI-_bLvBr-Bs3Xk8s9WH0XhhKg1Vi6eu7hp_io5yKLw5-4tj9DK5W6f3wfx5-pDezgPgTLSBNDxKEiJoHDETak14RoWMKY849CuTKNJEZ1rKhMdJTDLDiGDvuWEyYlRL4GN0NfTNXO29M7lqnC3B7RQl6vclav-S3l4MtgGfQZE7qDLr9wVMcEmF6FkwMOtb871Pg_tQUczjUK0XK_W0ZLPHdDlRUe8vBw-ZV9u6c1V_8D_jfwDDZXsP</recordid><startdate>19981020</startdate><enddate>19981020</enddate><creator>Lin, Hong-Cheu</creator><creator>Lin, Yen-Shyi</creator><creator>Lin, Yu-Sheng</creator><creator>Chen, Yao-Te</creator><creator>Chao, Ito</creator><creator>Li, Ta-Wei</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19981020</creationdate><title>Supramolecular Side-Chain Liquid Crystalline Polymers with Various Kinked Pendant Groups</title><author>Lin, Hong-Cheu ; Lin, Yen-Shyi ; Lin, Yu-Sheng ; Chen, Yao-Te ; Chao, Ito ; Li, Ta-Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-8e3699041762e5dd03c14871363a024066d0dcd88937970ce2042bfe28621d8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Applied sciences</topic><topic>Chemical modifications</topic><topic>Exact sciences and technology</topic><topic>Inorganic and organomineral polymers</topic><topic>Physicochemistry of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Hong-Cheu</creatorcontrib><creatorcontrib>Lin, Yen-Shyi</creatorcontrib><creatorcontrib>Lin, Yu-Sheng</creatorcontrib><creatorcontrib>Chen, Yao-Te</creatorcontrib><creatorcontrib>Chao, Ito</creatorcontrib><creatorcontrib>Li, Ta-Wei</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Hong-Cheu</au><au>Lin, Yen-Shyi</au><au>Lin, Yu-Sheng</au><au>Chen, Yao-Te</au><au>Chao, Ito</au><au>Li, Ta-Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Supramolecular Side-Chain Liquid Crystalline Polymers with Various Kinked Pendant Groups</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>1998-10-20</date><risdate>1998</risdate><volume>31</volume><issue>21</issue><spage>7298</spage><epage>7311</epage><pages>7298-7311</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Supramolecular side-chain liquid crystalline polymers with various kinked pendant groups are constructed from positional isomers of proton acceptor monomers and donor polymers (with different molecular weights) through hydrogen bonding. Monomer−monomer complexes of similar structures are built to compare the influence of the proton donors bound to the polymer backbones. Due to the bending effects introduced by the positional isomers, we are able to tune the molecular shape and thus to modify the mesogenic properties. New liquid crystalline properties are introduced by the kinked molecular geometry, and their kinked architecture is supported by the quantum mechanical calculations, the powder X-ray diffraction (XRD) patterns, and the deviation temperatures (ΔT). Mesogenic properties of monomer−polymer complexes have similar trends as those of monomer−monomer complexes. Compared with analogous hydrogen-bonded (H-bonded) monomer−monomer complexes, higher isotropization temperatures and broader ranges of mesogenic phases (e.g., SA phase) are observed in the kinked supramolecular polymers. Significantly, H-bonded positional isomerism leads to dissimilar structures and properties of supramolecular side-chain liquid crystalline polymers.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma980720e</doi><tpages>14</tpages></addata></record> |
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subjects | Applied sciences Chemical modifications Exact sciences and technology Inorganic and organomineral polymers Physicochemistry of polymers |
title | Supramolecular Side-Chain Liquid Crystalline Polymers with Various Kinked Pendant Groups |
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