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Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole
We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble int...
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Published in: | Chemistry : a European journal 2018-02, Vol.24 (9), p.2182-2191 |
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description | We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble into dimeric capsules by encapsulating one molecule of a suitable bis‐N‐oxide or two molecules of a mono‐N‐oxide. The dimeric capsules are mainly stabilized by a cyclic array of sixteen hydrogen bonds established between the eight unidirectionally oriented urea groups. Photoirradiation experiments demonstrated the trans‐to‐cis isomerization of the azo‐phenyl groups and the formation of a plethora of stereo isomeric cis‐azo‐enriched capsular assemblies. The highly cis‐azo enriched capsular assemblies seem to show a reduced stability and their involvement in equilibria with non‐capsular counterparts that also bind the N‐oxides. The thermally induced cis‐to‐trans interconversion processes demonstrated the reversibility of the photoisomerization and the photostability of most binding partners. An equimolar mixture of the two tetraureas produced two homodimeric capsules and the heterodimeric counterpart in a ratio close to statistical distribution.
An aryl extension in light: The syntheses of a lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole, and its photo‐inactive counterpart are reported. Both tetraureas self‐assemble into dimeric capsules by encapsulating one molecule of a bis‐N‐oxide or two molecules of mono‐N‐oxide. The results of light irradiation experiments performed with the photoresponsive homo‐ and heterocapsules are described. |
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An aryl extension in light: The syntheses of a lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole, and its photo‐inactive counterpart are reported. Both tetraureas self‐assemble into dimeric capsules by encapsulating one molecule of a bis‐N‐oxide or two molecules of mono‐N‐oxide. The results of light irradiation experiments performed with the photoresponsive homo‐ and heterocapsules are described.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201704777</identifier><identifier>PMID: 29243315</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Aromatic compounds ; Assemblies ; Carbonyls ; Chemical bonds ; Chemistry ; Dimerization ; host–guest systems ; Hydrogen bonding ; Hydrogen bonds ; Isomerization ; Lipophilic ; molecular devices ; N-Oxides ; Oxides ; Pyrroles ; receptors ; self-assembly ; supramolecular chemistry ; Urea</subject><ispartof>Chemistry : a European journal, 2018-02, Vol.24 (9), p.2182-2191</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4767-b436b7557df31601a5cff97a42f5699eacce51f196f4a1ddface2cbbc400bf213</citedby><cites>FETCH-LOGICAL-c4767-b436b7557df31601a5cff97a42f5699eacce51f196f4a1ddface2cbbc400bf213</cites><orcidid>0000-0001-8377-6610 ; 0000-0001-8750-6415 ; 0000-0002-2108-4296</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29243315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sekiya, Ryo</creatorcontrib><creatorcontrib>Díaz‐Moscoso, Alejandro</creatorcontrib><creatorcontrib>Ballester, Pablo</creatorcontrib><title>Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble into dimeric capsules by encapsulating one molecule of a suitable bis‐N‐oxide or two molecules of a mono‐N‐oxide. The dimeric capsules are mainly stabilized by a cyclic array of sixteen hydrogen bonds established between the eight unidirectionally oriented urea groups. Photoirradiation experiments demonstrated the trans‐to‐cis isomerization of the azo‐phenyl groups and the formation of a plethora of stereo isomeric cis‐azo‐enriched capsular assemblies. The highly cis‐azo enriched capsular assemblies seem to show a reduced stability and their involvement in equilibria with non‐capsular counterparts that also bind the N‐oxides. The thermally induced cis‐to‐trans interconversion processes demonstrated the reversibility of the photoisomerization and the photostability of most binding partners. An equimolar mixture of the two tetraureas produced two homodimeric capsules and the heterodimeric counterpart in a ratio close to statistical distribution.
An aryl extension in light: The syntheses of a lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole, and its photo‐inactive counterpart are reported. Both tetraureas self‐assemble into dimeric capsules by encapsulating one molecule of a bis‐N‐oxide or two molecules of mono‐N‐oxide. The results of light irradiation experiments performed with the photoresponsive homo‐ and heterocapsules are described.</description><subject>Aromatic compounds</subject><subject>Assemblies</subject><subject>Carbonyls</subject><subject>Chemical bonds</subject><subject>Chemistry</subject><subject>Dimerization</subject><subject>host–guest systems</subject><subject>Hydrogen bonding</subject><subject>Hydrogen bonds</subject><subject>Isomerization</subject><subject>Lipophilic</subject><subject>molecular devices</subject><subject>N-Oxides</subject><subject>Oxides</subject><subject>Pyrroles</subject><subject>receptors</subject><subject>self-assembly</subject><subject>supramolecular chemistry</subject><subject>Urea</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkU2LFDEQhoMo7jh69SgBL156TOWjY47L7OgKIwq7nkSadLrCZOnutEm3bnvyJ_gb_SX2MusKXjwVFE89FO9LyFNgG2CMv3QH7DacgWZSa32PrEBxKIQu1X2yYkbqolTCnJBHOV8xxkwpxENywg2XQoBakf5i7scD5pCp7Rt6FjpM4bsdQ-zpxTg1ATONnlq6D0McDqENjn44xDEmzEPsc_iK9DTN7a8fP3fXI_YNNvQSx2SnhHZZbm0brj_Jz8OcUmzxMXngbZvxye1ck4-vd5fb82L__s3b7em-cFKXuqilKGutlG68gJKBVc57o63kXpXGoHUOFXgwpZcWmsZbh9zVtZOM1Z6DWJMXR--Q4pcJ81h1ITtsW9tjnHIFZknrlVRLCmvy_B_0Kk6pX75bKGMUcAC-UJsj5VLMOaGvhhQ6m-YKWHXTRHXTRHXXxHLw7FY71R02d_if6BfAHIFvocX5P7pqe75791f-G6tAmVA</recordid><startdate>20180209</startdate><enddate>20180209</enddate><creator>Sekiya, Ryo</creator><creator>Díaz‐Moscoso, Alejandro</creator><creator>Ballester, Pablo</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8377-6610</orcidid><orcidid>https://orcid.org/0000-0001-8750-6415</orcidid><orcidid>https://orcid.org/0000-0002-2108-4296</orcidid></search><sort><creationdate>20180209</creationdate><title>Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole</title><author>Sekiya, Ryo ; Díaz‐Moscoso, Alejandro ; Ballester, Pablo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4767-b436b7557df31601a5cff97a42f5699eacce51f196f4a1ddface2cbbc400bf213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aromatic compounds</topic><topic>Assemblies</topic><topic>Carbonyls</topic><topic>Chemical bonds</topic><topic>Chemistry</topic><topic>Dimerization</topic><topic>host–guest systems</topic><topic>Hydrogen bonding</topic><topic>Hydrogen bonds</topic><topic>Isomerization</topic><topic>Lipophilic</topic><topic>molecular devices</topic><topic>N-Oxides</topic><topic>Oxides</topic><topic>Pyrroles</topic><topic>receptors</topic><topic>self-assembly</topic><topic>supramolecular chemistry</topic><topic>Urea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sekiya, Ryo</creatorcontrib><creatorcontrib>Díaz‐Moscoso, Alejandro</creatorcontrib><creatorcontrib>Ballester, Pablo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sekiya, Ryo</au><au>Díaz‐Moscoso, Alejandro</au><au>Ballester, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2018-02-09</date><risdate>2018</risdate><volume>24</volume><issue>9</issue><spage>2182</spage><epage>2191</epage><pages>2182-2191</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble into dimeric capsules by encapsulating one molecule of a suitable bis‐N‐oxide or two molecules of a mono‐N‐oxide. The dimeric capsules are mainly stabilized by a cyclic array of sixteen hydrogen bonds established between the eight unidirectionally oriented urea groups. Photoirradiation experiments demonstrated the trans‐to‐cis isomerization of the azo‐phenyl groups and the formation of a plethora of stereo isomeric cis‐azo‐enriched capsular assemblies. The highly cis‐azo enriched capsular assemblies seem to show a reduced stability and their involvement in equilibria with non‐capsular counterparts that also bind the N‐oxides. The thermally induced cis‐to‐trans interconversion processes demonstrated the reversibility of the photoisomerization and the photostability of most binding partners. An equimolar mixture of the two tetraureas produced two homodimeric capsules and the heterodimeric counterpart in a ratio close to statistical distribution.
An aryl extension in light: The syntheses of a lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole, and its photo‐inactive counterpart are reported. Both tetraureas self‐assemble into dimeric capsules by encapsulating one molecule of a bis‐N‐oxide or two molecules of mono‐N‐oxide. The results of light irradiation experiments performed with the photoresponsive homo‐ and heterocapsules are described.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29243315</pmid><doi>10.1002/chem.201704777</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8377-6610</orcidid><orcidid>https://orcid.org/0000-0001-8750-6415</orcidid><orcidid>https://orcid.org/0000-0002-2108-4296</orcidid></addata></record> |
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subjects | Aromatic compounds Assemblies Carbonyls Chemical bonds Chemistry Dimerization host–guest systems Hydrogen bonding Hydrogen bonds Isomerization Lipophilic molecular devices N-Oxides Oxides Pyrroles receptors self-assembly supramolecular chemistry Urea |
title | Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole |
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