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The role of indolyl substituents in squaramide-based anionophores
A new family of squaramide-based anionophores ( L1-L8 ) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties. L1 , L2 , L6 , and L8 , bearing a 7-indolyl/indol-7-yl moiety as the sub...
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Published in: | Organic & biomolecular chemistry 2022-10, Vol.2 (4), p.7981-7986 |
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container_title | Organic & biomolecular chemistry |
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creator | Picci, Giacomo Carreira-Barral, Israel Alonso-Carrillo, Daniel Busonera, Chiara Milia, Jessica Quesada, Roberto Caltagirone, Claudia |
description | A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.
L1
,
L2
,
L6
, and
L8
, bearing a 7-indolyl/indol-7-yl moiety as the substituent, were found to be the most efficient of the series in binding chloride with high stability constants.
L1
,
L6
, and
L8
were also found to be the most potent anionophores of the series, able to mediate transmembrane anion transport. In particular,
L6
bearing the 3,5-bis(trifluoromethyl)phenyl group was found to be the most active transporter, and its efficiency as an anionophore/anion transporter was favourably compared with that of their symmetrically-substituted squaramide analogues
L9
and
L10
, previously reported in the literature.
A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties. |
doi_str_mv | 10.1039/d2ob01444k |
format | article |
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L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.
L1
,
L2
,
L6
, and
L8
, bearing a 7-indolyl/indol-7-yl moiety as the substituent, were found to be the most efficient of the series in binding chloride with high stability constants.
L1
,
L6
, and
L8
were also found to be the most potent anionophores of the series, able to mediate transmembrane anion transport. In particular,
L6
bearing the 3,5-bis(trifluoromethyl)phenyl group was found to be the most active transporter, and its efficiency as an anionophore/anion transporter was favourably compared with that of their symmetrically-substituted squaramide analogues
L9
and
L10
, previously reported in the literature.
A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/d2ob01444k</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Anions ; Binding ; Stability constants ; Transport properties</subject><ispartof>Organic & biomolecular chemistry, 2022-10, Vol.2 (4), p.7981-7986</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-f31adb2b6a13dc2cb8ddb48b974e1b313d8340f7f1c2a5d10a5ffa0a394969e33</citedby><cites>FETCH-LOGICAL-c350t-f31adb2b6a13dc2cb8ddb48b974e1b313d8340f7f1c2a5d10a5ffa0a394969e33</cites><orcidid>0000-0002-4835-8752 ; 0000-0002-4302-0234 ; 0000-0003-2764-7157 ; 0000-0002-6132-8953</orcidid></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></links><search><creatorcontrib>Picci, Giacomo</creatorcontrib><creatorcontrib>Carreira-Barral, Israel</creatorcontrib><creatorcontrib>Alonso-Carrillo, Daniel</creatorcontrib><creatorcontrib>Busonera, Chiara</creatorcontrib><creatorcontrib>Milia, Jessica</creatorcontrib><creatorcontrib>Quesada, Roberto</creatorcontrib><creatorcontrib>Caltagirone, Claudia</creatorcontrib><title>The role of indolyl substituents in squaramide-based anionophores</title><title>Organic & biomolecular chemistry</title><description>A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.
L1
,
L2
,
L6
, and
L8
, bearing a 7-indolyl/indol-7-yl moiety as the substituent, were found to be the most efficient of the series in binding chloride with high stability constants.
L1
,
L6
, and
L8
were also found to be the most potent anionophores of the series, able to mediate transmembrane anion transport. In particular,
L6
bearing the 3,5-bis(trifluoromethyl)phenyl group was found to be the most active transporter, and its efficiency as an anionophore/anion transporter was favourably compared with that of their symmetrically-substituted squaramide analogues
L9
and
L10
, previously reported in the literature.
A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.</description><subject>Anions</subject><subject>Binding</subject><subject>Stability constants</subject><subject>Transport properties</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0MtLw0AQBvBFFKzVi3ch4EWE6OwjSfdY6xMLvdRz2CdNTbPtTnLof29iRcHTDB8_huEj5JLCHQUu7y0LGqgQ4vOIjKgoihQyLo9_dwan5AxxDUBlkYsRmS5XLomhdknwSdXYUO_rBDuNbdV2rmmxDxPcdSqqTWVdqhU6m6imCk3YrkJ0eE5OvKrRXfzMMfl4flrOXtP54uVtNp2nhmfQpp5TZTXTuaLcGmb0xFotJloWwlHN-3DCBfjCU8NUZimozHsFikshc-k4H5Obw91tDLvOYVtuKjSurlXjQoclKxjNBy17ev2PrkMXm_67QeUAOeWDuj0oEwNidL7cxmqj4r6kUA5tlo9s8fDd5nuPrw44ovl1f23zL_IdcSo</recordid><startdate>20221019</startdate><enddate>20221019</enddate><creator>Picci, Giacomo</creator><creator>Carreira-Barral, Israel</creator><creator>Alonso-Carrillo, Daniel</creator><creator>Busonera, Chiara</creator><creator>Milia, Jessica</creator><creator>Quesada, Roberto</creator><creator>Caltagirone, Claudia</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4835-8752</orcidid><orcidid>https://orcid.org/0000-0002-4302-0234</orcidid><orcidid>https://orcid.org/0000-0003-2764-7157</orcidid><orcidid>https://orcid.org/0000-0002-6132-8953</orcidid></search><sort><creationdate>20221019</creationdate><title>The role of indolyl substituents in squaramide-based anionophores</title><author>Picci, Giacomo ; Carreira-Barral, Israel ; Alonso-Carrillo, Daniel ; Busonera, Chiara ; Milia, Jessica ; Quesada, Roberto ; Caltagirone, Claudia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-f31adb2b6a13dc2cb8ddb48b974e1b313d8340f7f1c2a5d10a5ffa0a394969e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Anions</topic><topic>Binding</topic><topic>Stability constants</topic><topic>Transport properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Picci, Giacomo</creatorcontrib><creatorcontrib>Carreira-Barral, Israel</creatorcontrib><creatorcontrib>Alonso-Carrillo, Daniel</creatorcontrib><creatorcontrib>Busonera, Chiara</creatorcontrib><creatorcontrib>Milia, Jessica</creatorcontrib><creatorcontrib>Quesada, Roberto</creatorcontrib><creatorcontrib>Caltagirone, Claudia</creatorcontrib><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Organic & biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Picci, Giacomo</au><au>Carreira-Barral, Israel</au><au>Alonso-Carrillo, Daniel</au><au>Busonera, Chiara</au><au>Milia, Jessica</au><au>Quesada, Roberto</au><au>Caltagirone, Claudia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of indolyl substituents in squaramide-based anionophores</atitle><jtitle>Organic & biomolecular chemistry</jtitle><date>2022-10-19</date><risdate>2022</risdate><volume>2</volume><issue>4</issue><spage>7981</spage><epage>7986</epage><pages>7981-7986</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.
L1
,
L2
,
L6
, and
L8
, bearing a 7-indolyl/indol-7-yl moiety as the substituent, were found to be the most efficient of the series in binding chloride with high stability constants.
L1
,
L6
, and
L8
were also found to be the most potent anionophores of the series, able to mediate transmembrane anion transport. In particular,
L6
bearing the 3,5-bis(trifluoromethyl)phenyl group was found to be the most active transporter, and its efficiency as an anionophore/anion transporter was favourably compared with that of their symmetrically-substituted squaramide analogues
L9
and
L10
, previously reported in the literature.
A new family of squaramide-based anionophores (
L1-L8
) have been synthesised and fully characterised with the aim to investigate the effect of indolyl substituents on their anion binding and transmembrane transport properties.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2ob01444k</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-4835-8752</orcidid><orcidid>https://orcid.org/0000-0002-4302-0234</orcidid><orcidid>https://orcid.org/0000-0003-2764-7157</orcidid><orcidid>https://orcid.org/0000-0002-6132-8953</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Royal Society of Chemistry |
subjects | Anions Binding Stability constants Transport properties |
title | The role of indolyl substituents in squaramide-based anionophores |
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