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Bicyclo[2.2.2]octene-Based “Crab-like” Molecules: Synthesis, Complexation, Luminescence Properties, and Solid-State Structures
The U-shaped, multifunctionalized tetraetheno-bridged dicyclopenta[b,i]anthracenediol 10 was synthesized to serve as a platform molecule. The molecule was prepared from the Diels−Alder adduct 5a of tricycloundecatriene 3 and bicyclo[2.2.2]octene-fused p-benzoquinone 4. Functionalization of 10 to con...
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Published in: | Journal of organic chemistry 2005-11, Vol.70 (24), p.9717-9726 |
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creator | Chou, Teh-Chang Hwa, Ching-Lun Lin, Jin-Ju Liao, Kung-Ching Tseng, Jui-Chang |
description | The U-shaped, multifunctionalized tetraetheno-bridged dicyclopenta[b,i]anthracenediol 10 was synthesized to serve as a platform molecule. The molecule was prepared from the Diels−Alder adduct 5a of tricycloundecatriene 3 and bicyclo[2.2.2]octene-fused p-benzoquinone 4. Functionalization of 10 to construct crab-like molecules was achieved via the base-promoted bis-O-alkylation of two endo-oriented hydroxyl groups at termini in 10 with the following alkyl halides: allyl, propagyl, and benzyl bromides; 1-bromo- and 1-iodo-4-(bromomethyl)benzene; 9-(bromomethyl)anthracene; 1-(bromomethyl)pyrene; and isomeric bromomethylpyridines. Single-crystal X-ray structures were obtained for bis-phenyl (21) and bis-pyrenyl (25) crabs, and for the silver(I) complex (32 and 33) crabs. The silver(I) complex 32 from bis-o-pyridyl crab 30 is a [2+2] dimeric dimetallocyclophane, and 33 from bis-m-pyridyl crab 29 is a [1+1] metallo-bridged cyclophane. The self-assembled intramolecular π-stacking of pyrenyl rings in 25 with an interplanar distance of 3.40 Å and the consequent π−π interactions were revealed by the X-ray crystal structure and its luminescence property. |
doi_str_mv | 10.1021/jo051006f |
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The molecule was prepared from the Diels−Alder adduct 5a of tricycloundecatriene 3 and bicyclo[2.2.2]octene-fused p-benzoquinone 4. Functionalization of 10 to construct crab-like molecules was achieved via the base-promoted bis-O-alkylation of two endo-oriented hydroxyl groups at termini in 10 with the following alkyl halides: allyl, propagyl, and benzyl bromides; 1-bromo- and 1-iodo-4-(bromomethyl)benzene; 9-(bromomethyl)anthracene; 1-(bromomethyl)pyrene; and isomeric bromomethylpyridines. Single-crystal X-ray structures were obtained for bis-phenyl (21) and bis-pyrenyl (25) crabs, and for the silver(I) complex (32 and 33) crabs. The silver(I) complex 32 from bis-o-pyridyl crab 30 is a [2+2] dimeric dimetallocyclophane, and 33 from bis-m-pyridyl crab 29 is a [1+1] metallo-bridged cyclophane. The self-assembled intramolecular π-stacking of pyrenyl rings in 25 with an interplanar distance of 3.40 Å and the consequent π−π interactions were revealed by the X-ray crystal structure and its luminescence property.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo051006f</identifier><identifier>PMID: 16292799</identifier><identifier>CODEN: JOCEAH</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Anthracenes - chemical synthesis ; Anthracenes - chemistry ; Bridged Bicyclo Compounds - chemical synthesis ; Bridged Bicyclo Compounds - chemistry ; Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis ; Bridged Bicyclo Compounds, Heterocyclic - chemistry ; Chemistry ; Coordination compounds ; Crystallography, X-Ray ; Exact sciences and technology ; Hydrogen Bonding ; Inorganic chemistry and origins of life ; Luminescence ; Models, Molecular ; Molecular Conformation ; Octanes - chemical synthesis ; Octanes - chemistry ; Preparations and properties ; Stereoisomerism</subject><ispartof>Journal of organic chemistry, 2005-11, Vol.70 (24), p.9717-9726</ispartof><rights>Copyright © 2005 American Chemical Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a447t-983080c80043b7f3305d2f6cfacafca22eb4e2158dcfa1e6f7d85730272ca87e3</citedby><cites>FETCH-LOGICAL-a447t-983080c80043b7f3305d2f6cfacafca22eb4e2158dcfa1e6f7d85730272ca87e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17313562$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16292799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chou, Teh-Chang</creatorcontrib><creatorcontrib>Hwa, Ching-Lun</creatorcontrib><creatorcontrib>Lin, Jin-Ju</creatorcontrib><creatorcontrib>Liao, Kung-Ching</creatorcontrib><creatorcontrib>Tseng, Jui-Chang</creatorcontrib><title>Bicyclo[2.2.2]octene-Based “Crab-like” Molecules: Synthesis, Complexation, Luminescence Properties, and Solid-State Structures</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>The U-shaped, multifunctionalized tetraetheno-bridged dicyclopenta[b,i]anthracenediol 10 was synthesized to serve as a platform molecule. The molecule was prepared from the Diels−Alder adduct 5a of tricycloundecatriene 3 and bicyclo[2.2.2]octene-fused p-benzoquinone 4. Functionalization of 10 to construct crab-like molecules was achieved via the base-promoted bis-O-alkylation of two endo-oriented hydroxyl groups at termini in 10 with the following alkyl halides: allyl, propagyl, and benzyl bromides; 1-bromo- and 1-iodo-4-(bromomethyl)benzene; 9-(bromomethyl)anthracene; 1-(bromomethyl)pyrene; and isomeric bromomethylpyridines. Single-crystal X-ray structures were obtained for bis-phenyl (21) and bis-pyrenyl (25) crabs, and for the silver(I) complex (32 and 33) crabs. The silver(I) complex 32 from bis-o-pyridyl crab 30 is a [2+2] dimeric dimetallocyclophane, and 33 from bis-m-pyridyl crab 29 is a [1+1] metallo-bridged cyclophane. The self-assembled intramolecular π-stacking of pyrenyl rings in 25 with an interplanar distance of 3.40 Å and the consequent π−π interactions were revealed by the X-ray crystal structure and its luminescence property.</description><subject>Anthracenes - chemical synthesis</subject><subject>Anthracenes - chemistry</subject><subject>Bridged Bicyclo Compounds - chemical synthesis</subject><subject>Bridged Bicyclo Compounds - chemistry</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - chemistry</subject><subject>Chemistry</subject><subject>Coordination compounds</subject><subject>Crystallography, X-Ray</subject><subject>Exact sciences and technology</subject><subject>Hydrogen Bonding</subject><subject>Inorganic chemistry and origins of life</subject><subject>Luminescence</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Octanes - chemical synthesis</subject><subject>Octanes - chemistry</subject><subject>Preparations and properties</subject><subject>Stereoisomerism</subject><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpt0E9rFDEYBvAgFrutHvwCMhcFoVPzZzKZ6c0u1YpbLE7Vg0jIZt7BtJnJmmSge9uLB79D--X2kxjZpXsxOQTe_Hh5eBB6TvAxwZS8uXaYE4zL7hGaEE5xXta4eIwmGFOaM1qyfXQQwjVOh3P-BO2TktZU1PUE_T41eqmt-06P0_3hdIQB8lMVoM3Wq7upV_PcmhtYr-6zC2dBjxbCyXr1J2uWQ_wJwYSjbOr6hYVbFY0bjrLZ2JsBgoZBQ3bp3QJ8NJCYGtqscda0eRNVhKyJftRx9BCeor1O2QDPtu8h-vLu7Gp6ns8-vf8wfTvLVVGImNcVwxXWFcYFm4uOMcxb2pW6U1p1WlEK8wIo4VWbRgTKTrQVFwxTQbWqBLBD9Gqzd-HdrxFClL1JQa1VA7gxyLKqsMCUJfh6A7V3IXjo5MKbXvmlJFj-61w-dJ7si-3Scd5Du5PbkhN4uQUqaGU7rwZtws4JRhgvaXL5xpkQ4fbhX_kbWQomuLy6bOTnb18vBJtR-XG3V-mQ8ox-SN39J-Bfgpqn9w</recordid><startdate>20051125</startdate><enddate>20051125</enddate><creator>Chou, Teh-Chang</creator><creator>Hwa, Ching-Lun</creator><creator>Lin, Jin-Ju</creator><creator>Liao, Kung-Ching</creator><creator>Tseng, Jui-Chang</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20051125</creationdate><title>Bicyclo[2.2.2]octene-Based “Crab-like” Molecules: Synthesis, Complexation, Luminescence Properties, and Solid-State Structures</title><author>Chou, Teh-Chang ; Hwa, Ching-Lun ; Lin, Jin-Ju ; Liao, Kung-Ching ; Tseng, Jui-Chang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a447t-983080c80043b7f3305d2f6cfacafca22eb4e2158dcfa1e6f7d85730272ca87e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Anthracenes - chemical synthesis</topic><topic>Anthracenes - chemistry</topic><topic>Bridged Bicyclo Compounds - chemical synthesis</topic><topic>Bridged Bicyclo Compounds - chemistry</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - chemistry</topic><topic>Chemistry</topic><topic>Coordination compounds</topic><topic>Crystallography, X-Ray</topic><topic>Exact sciences and technology</topic><topic>Hydrogen Bonding</topic><topic>Inorganic chemistry and origins of life</topic><topic>Luminescence</topic><topic>Models, Molecular</topic><topic>Molecular Conformation</topic><topic>Octanes - chemical synthesis</topic><topic>Octanes - chemistry</topic><topic>Preparations and properties</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chou, Teh-Chang</creatorcontrib><creatorcontrib>Hwa, Ching-Lun</creatorcontrib><creatorcontrib>Lin, Jin-Ju</creatorcontrib><creatorcontrib>Liao, Kung-Ching</creatorcontrib><creatorcontrib>Tseng, Jui-Chang</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chou, Teh-Chang</au><au>Hwa, Ching-Lun</au><au>Lin, Jin-Ju</au><au>Liao, Kung-Ching</au><au>Tseng, Jui-Chang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bicyclo[2.2.2]octene-Based “Crab-like” Molecules: Synthesis, Complexation, Luminescence Properties, and Solid-State Structures</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2005-11-25</date><risdate>2005</risdate><volume>70</volume><issue>24</issue><spage>9717</spage><epage>9726</epage><pages>9717-9726</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>The U-shaped, multifunctionalized tetraetheno-bridged dicyclopenta[b,i]anthracenediol 10 was synthesized to serve as a platform molecule. The molecule was prepared from the Diels−Alder adduct 5a of tricycloundecatriene 3 and bicyclo[2.2.2]octene-fused p-benzoquinone 4. Functionalization of 10 to construct crab-like molecules was achieved via the base-promoted bis-O-alkylation of two endo-oriented hydroxyl groups at termini in 10 with the following alkyl halides: allyl, propagyl, and benzyl bromides; 1-bromo- and 1-iodo-4-(bromomethyl)benzene; 9-(bromomethyl)anthracene; 1-(bromomethyl)pyrene; and isomeric bromomethylpyridines. Single-crystal X-ray structures were obtained for bis-phenyl (21) and bis-pyrenyl (25) crabs, and for the silver(I) complex (32 and 33) crabs. The silver(I) complex 32 from bis-o-pyridyl crab 30 is a [2+2] dimeric dimetallocyclophane, and 33 from bis-m-pyridyl crab 29 is a [1+1] metallo-bridged cyclophane. The self-assembled intramolecular π-stacking of pyrenyl rings in 25 with an interplanar distance of 3.40 Å and the consequent π−π interactions were revealed by the X-ray crystal structure and its luminescence property.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16292799</pmid><doi>10.1021/jo051006f</doi><tpages>10</tpages></addata></record> |
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subjects | Anthracenes - chemical synthesis Anthracenes - chemistry Bridged Bicyclo Compounds - chemical synthesis Bridged Bicyclo Compounds - chemistry Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis Bridged Bicyclo Compounds, Heterocyclic - chemistry Chemistry Coordination compounds Crystallography, X-Ray Exact sciences and technology Hydrogen Bonding Inorganic chemistry and origins of life Luminescence Models, Molecular Molecular Conformation Octanes - chemical synthesis Octanes - chemistry Preparations and properties Stereoisomerism |
title | Bicyclo[2.2.2]octene-Based “Crab-like” Molecules: Synthesis, Complexation, Luminescence Properties, and Solid-State Structures |
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