Effects of Lateral Substituents on Mesomorphic Behavior. III. N-4-(4-Alkoxybenzoyloxy)benzylidene]-anilines
The mesomorphic properties of N-4-(4-alkoxybenzoyloxy)benzylidene]-2- and -3-X-anilines, where X = Me, F, Cl, Br or I, were examined. The 2-Me derivatives give higher nematic-isotropic transition temperatures than the 3-Me derivatives, whereas the reverse is true for the F compounds. The intersectio...
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Veröffentlicht in: | Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals Molecular crystals and liquid crystals, 1999-01, Vol.326 (1), p.155-164 |
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creator | Matsunaga, Y. Miyake, T. Rikimaru, H. Iwano, N. |
description | The mesomorphic properties of N-4-(4-alkoxybenzoyloxy)benzylidene]-2- and -3-X-anilines, where X = Me, F, Cl, Br or I, were examined. The 2-Me derivatives give higher nematic-isotropic transition temperatures than the 3-Me derivatives, whereas the reverse is true for the F compounds. The intersection between the plots of the transition temperatures of the 2-X and 3-X derivatives against the alky chain length is found for the CL, Br, and I compounds, respectively. The smectic A-nematic transition temperature recorded for the heptyloxy member is promoted by the 3-X substitution as much as 32°C (X = F) and 16° (X = Cl). |
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The smectic A-nematic transition temperature recorded for the heptyloxy member is promoted by the 3-X substitution as much as 32°C (X = F) and 16° (X = Cl).</description><identifier>ISSN: 1058-725X</identifier><identifier>DOI: 10.1080/10587259908025412</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>lateral substituent ; Nematic ; smectic</subject><ispartof>Molecular crystals and liquid crystals science and technology. 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III. N-4-(4-Alkoxybenzoyloxy)benzylidene]-anilines</title><title>Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals</title><description>The mesomorphic properties of N-4-(4-alkoxybenzoyloxy)benzylidene]-2- and -3-X-anilines, where X = Me, F, Cl, Br or I, were examined. The 2-Me derivatives give higher nematic-isotropic transition temperatures than the 3-Me derivatives, whereas the reverse is true for the F compounds. The intersection between the plots of the transition temperatures of the 2-X and 3-X derivatives against the alky chain length is found for the CL, Br, and I compounds, respectively. The smectic A-nematic transition temperature recorded for the heptyloxy member is promoted by the 3-X substitution as much as 32°C (X = F) and 16° (X = Cl).</description><subject>lateral substituent</subject><subject>Nematic</subject><subject>smectic</subject><issn>1058-725X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkD9PwzAQxT2ARCl8ALaMMLjYThwnEkup-BOpwABILChynLNqmtqVnULDpydR2SrEdO-e7nenewidUTKhJCOXlPBMMJ7nfcN4QtkBGg0e7s23I3QcwgchjPIkGaHljdag2hA5Hc1lC1420fOmCq1pN2AH30YPENzK-fXCqOgaFvLTOD-JiqKYRI84wecJnjZLt-0qsN-ua3p1MciuMTVYeMfSmsZYCCfoUMsmwOlvHaPX25uX2T2eP90Vs-kcK5pThmPF6wQEydKUcCllXcWC6EwIHSc14xqYVhkwWvfDVSbyFKSWkCpWKZ4CFfEY0d1e5V0IHnS59mYlfVdSUg4JlXsJ9YzYMcZq51fyy_mmLlvZv-O1l1aZsE-V7bbtyat_yfjvwz9XD4GA</recordid><startdate>19990101</startdate><enddate>19990101</enddate><creator>Matsunaga, Y.</creator><creator>Miyake, T.</creator><creator>Rikimaru, H.</creator><creator>Iwano, N.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990101</creationdate><title>Effects of Lateral Substituents on Mesomorphic Behavior. III. N-4-(4-Alkoxybenzoyloxy)benzylidene]-anilines</title><author>Matsunaga, Y. ; Miyake, T. ; Rikimaru, H. ; Iwano, N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1912-3c5d4e7086605aaadb370f877f34d25fe2fc8e21d912b8796eafae6c2bc56e173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>lateral substituent</topic><topic>Nematic</topic><topic>smectic</topic><toplevel>online_resources</toplevel><creatorcontrib>Matsunaga, Y.</creatorcontrib><creatorcontrib>Miyake, T.</creatorcontrib><creatorcontrib>Rikimaru, H.</creatorcontrib><creatorcontrib>Iwano, N.</creatorcontrib><collection>CrossRef</collection><jtitle>Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsunaga, Y.</au><au>Miyake, T.</au><au>Rikimaru, H.</au><au>Iwano, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Lateral Substituents on Mesomorphic Behavior. III. N-4-(4-Alkoxybenzoyloxy)benzylidene]-anilines</atitle><jtitle>Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals</jtitle><date>1999-01-01</date><risdate>1999</risdate><volume>326</volume><issue>1</issue><spage>155</spage><epage>164</epage><pages>155-164</pages><issn>1058-725X</issn><abstract>The mesomorphic properties of N-4-(4-alkoxybenzoyloxy)benzylidene]-2- and -3-X-anilines, where X = Me, F, Cl, Br or I, were examined. The 2-Me derivatives give higher nematic-isotropic transition temperatures than the 3-Me derivatives, whereas the reverse is true for the F compounds. The intersection between the plots of the transition temperatures of the 2-X and 3-X derivatives against the alky chain length is found for the CL, Br, and I compounds, respectively. The smectic A-nematic transition temperature recorded for the heptyloxy member is promoted by the 3-X substitution as much as 32°C (X = F) and 16° (X = Cl).</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/10587259908025412</doi><tpages>10</tpages></addata></record> |
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title | Effects of Lateral Substituents on Mesomorphic Behavior. III. N-4-(4-Alkoxybenzoyloxy)benzylidene]-anilines |
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