<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Langton MJ</submitter><funding>EPSRC Centre</funding><funding>Funded Access</funding><funding>European Union’s Framework Program</funding><funding>European Research Council</funding><funding>University of Oxford Clarendon Fund Scholarship</funding><funding>EPSRC</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>18910-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4736451</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(52)</volume><pubmed_abstract>The synthesis of an all-halogen-bonding rotaxane for anion recognition is achieved by using active-metal templation. A flexible bis-iodotriazole-containing macrocycle is exploited for the metal-directed rotaxane synthesis. Endotopic binding of a Cu(I) template facilitates an active-metal CuAAC iodotriazole axle formation reaction that captures the interlocked rotaxane product. Following copper-template removal, exotopic coordination of a more sterically demanding rhenium(I) complex induces an inversion in the conformation of the macrocycle component, directing the iodotriazole halogen-bond donors into the rotaxane's interlocked binding cavity to facilitate anion recognition.</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>Active-Metal Template Synthesis of a Halogen-Bonding Rotaxane for Anion Recognition.</pubmed_title><pmcid>PMC4736451</pmcid><funding_grant_id>267426</funding_grant_id><funding_grant_id>1517513</funding_grant_id><funding_grant_id>FP7/2007-2013</funding_grant_id><funding_grant_id>EP/L015838/1</funding_grant_id><pubmed_authors>Xiong Y</pubmed_authors><pubmed_authors>Langton MJ</pubmed_authors><pubmed_authors>Beer PD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Active-Metal Template Synthesis of a Halogen-Bonding Rotaxane for Anion Recognition.</name><description>The synthesis of an all-halogen-bonding rotaxane for anion recognition is achieved by using active-metal templation. A flexible bis-iodotriazole-containing macrocycle is exploited for the metal-directed rotaxane synthesis. Endotopic binding of a Cu(I) template facilitates an active-metal CuAAC iodotriazole axle formation reaction that captures the interlocked rotaxane product. Following copper-template removal, exotopic coordination of a more sterically demanding rhenium(I) complex induces an inversion in the conformation of the macrocycle component, directing the iodotriazole halogen-bond donors into the rotaxane's interlocked binding cavity to facilitate anion recognition.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2026-05-05T09:05:10.49Z</modification><creation>2019-03-27T02:08:03Z</creation></dates><accession>S-EPMC4736451</accession><cross_references><pubmed>26500150</pubmed><doi>10.1002/chem.201504236</doi></cross_references></HashMap>