<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xing G</submitter><funding>Ministero dell&amp;apos;Istruzione, dell&amp;apos;Universitá e della Ricerca</funding><funding>Cariplo Foundation</funding><funding>Lombardy Region</funding><funding>National Natural Science Foundation of China</funding><pagination>730-736</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6354830</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(3)</volume><pubmed_abstract>Porous molecular materials represent a new front in the endeavor to achieve high-performance sorptive properties and gas transport. Self-assembly of polyfunctional molecules containing multiple charges, namely, tetrahedral tetra-sulfonate anions and bifunctional linear cations, resulted in a permanently porous crystalline material exhibiting tailored sub-nanometer channels with double helices of electrostatic charges that governed the association and transport of CO&lt;sub>2&lt;/sub> molecules. The charged channels were consolidated by robust hydrogen bonds. Guest recognition by electrostatic interactions remind us of the role played by the dipolar helical channels in regulatory biological membranes. The systematic electrostatic sites provided the perfectly fitting &lt;i>loci&lt;/i> of complementary c</pubmed_abstract><journal>Chemical science</journal><pubmed_title>A double helix of opposite charges to form channels with unique CO&lt;sub>2&lt;/sub> selectivity and dynamics.</pubmed_title><pmcid>PMC6354830</pmcid><funding_grant_id>PRIN 2016</funding_grant_id><funding_grant_id>21471065</funding_grant_id><funding_grant_id>21390394</funding_grant_id><funding_grant_id>Balance Project</funding_grant_id><funding_grant_id>Dipartimenti di Eccellenza 2018</funding_grant_id><pubmed_authors>Bezuidenhout C</pubmed_authors><pubmed_authors>Xing G</pubmed_authors><pubmed_authors>Sozzani P</pubmed_authors><pubmed_authors>Bassanetti I</pubmed_authors><pubmed_authors>Comotti A</pubmed_authors><pubmed_authors>Bracco S</pubmed_authors><pubmed_authors>Ben T</pubmed_authors><pubmed_authors>Negroni M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A double helix of opposite charges to form channels with unique CO&lt;sub>2&lt;/sub> selectivity and dynamics.</name><description>Porous molecular materials represent a new front in the endeavor to achieve high-performance sorptive properties and gas transport. Self-assembly of polyfunctional molecules containing multiple charges, namely, tetrahedral tetra-sulfonate anions and bifunctional linear cations, resulted in a permanently porous crystalline material exhibiting tailored sub-nanometer channels with double helices of electrostatic charges that governed the association and transport of CO&lt;sub>2&lt;/sub> molecules. The charged channels were consolidated by robust hydrogen bonds. Guest recognition by electrostatic interactions remind us of the role played by the dipolar helical channels in regulatory biological membranes. The systematic electrostatic sites provided the perfectly fitting &lt;i>loci&lt;/i> of complementary c</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-05-18T11:30:33.474Z</modification><creation>2025-05-18T11:30:33.474Z</creation></dates><accession>S-EPMC6354830</accession><cross_references><pubmed>30809339</pubmed><doi>10.1039/c8sc04376k</doi></cross_references></HashMap>