<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hartmann D</submitter><funding>Biotechnology and Biological Sciences Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>e202501122</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11976202</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>64(15)</volume><pubmed_abstract>Helical assemblies of organic dyes are ubiquitous chiral organic materials, with valuable properties including chiroptical switching due to the dynamic nature of supramolecular chirality. Herein, we report a novel chiral bis-perylene diimide macrocycle, which acts as a discrete molecular model for a chiral supramolecular assembly. Point chirality is installed through amino acid-derived imide groups which, upon macrocyclization, is translated into helical chirality in the perylene diimide dimer. In solution, the macrocycle's chiroptical properties are switchable, with both the sign (+/-) and amplitude (on/off) of the signal tuned using solvent and molecular recognition stimuli respectively. The chiral structure-property relationships identified from this macrocycle are important for the des</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>A Bis-Perylene Diimide Macrocycle Chiroptical Switch.</pubmed_title><pmcid>PMC11976202</pmcid><funding_grant_id>BB/X001172/1</funding_grant_id><funding_grant_id>BB/S017615/1</funding_grant_id><funding_grant_id>EP/X040259/1</funding_grant_id><funding_grant_id>EP/W037661/1</funding_grant_id><pubmed_authors>Barendt TA</pubmed_authors><pubmed_authors>Penty SE</pubmed_authors><pubmed_authors>Pal R</pubmed_authors><pubmed_authors>Hartmann D</pubmed_authors><pubmed_authors>Zwijnenburg MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Bis-Perylene Diimide Macrocycle Chiroptical Switch.</name><description>Helical assemblies of organic dyes are ubiquitous chiral organic materials, with valuable properties including chiroptical switching due to the dynamic nature of supramolecular chirality. Herein, we report a novel chiral bis-perylene diimide macrocycle, which acts as a discrete molecular model for a chiral supramolecular assembly. Point chirality is installed through amino acid-derived imide groups which, upon macrocyclization, is translated into helical chirality in the perylene diimide dimer. In solution, the macrocycle's chiroptical properties are switchable, with both the sign (+/-) and amplitude (on/off) of the signal tuned using solvent and molecular recognition stimuli respectively. The chiral structure-property relationships identified from this macrocycle are important for the des</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2025-07-06T03:04:36.454Z</modification><creation>2025-07-06T03:04:36.454Z</creation></dates><accession>S-EPMC11976202</accession><cross_references><pubmed>39888156</pubmed><doi>10.1002/anie.202501122</doi></cross_references></HashMap>