<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang GQ</submitter><funding>Jinan University</funding><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><pagination>2646-2653</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12687366</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(5)</volume><pubmed_abstract>Achieving chirality transfer and amplification through controlled supramolecular aggregation has long been a challenge in chemistry. This study presents the self-assembly of homochiral triple-helical aggregates (P- and M-type) with enantiomerically pure Cu(i) cyclic trinuclear complexes (CTCs) through metallophilic and hydrogen-bonding interactions. Both P- and M-type aggregates exhibit bright orange-red phosphorescence and circularly polarized luminescence (CPL) emission with an exceptional luminescence dissymmetry factor (&lt;i>g&lt;/i> &lt;sub>lum&lt;/sub>) of approximately ±1 × 10&lt;sup>-2&lt;/sup>. These values are the highest among coinage metal-based complexes with emissions across the red and near-infrared. Experimental results and computational simulations reveal that the extensive overlap of chir</pubmed_abstract><journal>Chemical science</journal><pubmed_title>Triple-helical aggregates of copper(i) cyclic trinuclear complexes for circularly polarized luminescence.</pubmed_title><pmcid>PMC12687366</pmcid><funding_grant_id>92461309</funding_grant_id><funding_grant_id>22431006</funding_grant_id><funding_grant_id>22171106</funding_grant_id><funding_grant_id>22271120</funding_grant_id><funding_grant_id>2024A1515012434</funding_grant_id><funding_grant_id>22401112</funding_grant_id><funding_grant_id>21621035</funding_grant_id><funding_grant_id>2024M761162</funding_grant_id><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Wu K</pubmed_authors><pubmed_authors>Xia RQ</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Huang YL</pubmed_authors><pubmed_authors>Huang GQ</pubmed_authors><pubmed_authors>Li SB</pubmed_authors><pubmed_authors>Hao DB</pubmed_authors><pubmed_authors>Zhou XP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Triple-helical aggregates of copper(i) cyclic trinuclear complexes for circularly polarized luminescence.</name><description>Achieving chirality transfer and amplification through controlled supramolecular aggregation has long been a challenge in chemistry. This study presents the self-assembly of homochiral triple-helical aggregates (P- and M-type) with enantiomerically pure Cu(i) cyclic trinuclear complexes (CTCs) through metallophilic and hydrogen-bonding interactions. Both P- and M-type aggregates exhibit bright orange-red phosphorescence and circularly polarized luminescence (CPL) emission with an exceptional luminescence dissymmetry factor (&lt;i>g&lt;/i> &lt;sub>lum&lt;/sub>) of approximately ±1 × 10&lt;sup>-2&lt;/sup>. These values are the highest among coinage metal-based complexes with emissions across the red and near-infrared. Experimental results and computational simulations reveal that the extensive overlap of chir</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-15T06:31:40.632Z</modification><creation>2026-06-30T03:19:57.934Z</creation></dates><accession>S-EPMC12687366</accession><cross_references><pubmed>41378145</pubmed><doi>10.1039/d5sc04965b</doi></cross_references></HashMap>