<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dockendorff J</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>European Research Council</funding><funding>Government of the Russian Federation</funding><pagination>8108-8122</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9062874</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53(18)</volume><pubmed_abstract>Arborescent copolymers with a core-shell-corona (CSC) architecture were synthesized and the topology of the molecules was challenged (constrained) through intramolecular interactions, resulting in phase separation breaking the symmetry of radial density. The inner poly(2-vinylpyridine) shell of these arborescent polystyrene-&lt;i>g&lt;/i>-[poly(2-vinylpyridine)-&lt;i>b&lt;/i>-polystyrene] molecules can self-assemble by binding metallic salts and acids in apolar and intermediate-polarity solvents. Upon loading with HAuCl&lt;sub>4&lt;/sub>, the characteristics of the polymer templates govern the "loading sites" of the metal within the molecules. Unique morphologies were observed for the metal-loaded G0-G4 arborescent copolymers investigated, namely, spherical, toroidal, raspberry-like, spherical nanocage, and</pubmed_abstract><journal>Macromolecules</journal><pubmed_title>Metal Coordination Induces Phase Segregation in Amphipolar Arborescent Copolymers with a Core-Shell-Corona Architecture.</pubmed_title><pmcid>PMC9062874</pmcid><funding_grant_id>02.A03.21.0011</funding_grant_id><funding_grant_id>695716</funding_grant_id><funding_grant_id>SFB 985</funding_grant_id><pubmed_authors>Moller M</pubmed_authors><pubmed_authors>Gumerov RA</pubmed_authors><pubmed_authors>Mourran A</pubmed_authors><pubmed_authors>Gauthier M</pubmed_authors><pubmed_authors>Dockendorff J</pubmed_authors><pubmed_authors>Potemkin II</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metal Coordination Induces Phase Segregation in Amphipolar Arborescent Copolymers with a Core-Shell-Corona Architecture.</name><description>Arborescent copolymers with a core-shell-corona (CSC) architecture were synthesized and the topology of the molecules was challenged (constrained) through intramolecular interactions, resulting in phase separation breaking the symmetry of radial density. The inner poly(2-vinylpyridine) shell of these arborescent polystyrene-&lt;i>g&lt;/i>-[poly(2-vinylpyridine)-&lt;i>b&lt;/i>-polystyrene] molecules can self-assemble by binding metallic salts and acids in apolar and intermediate-polarity solvents. Upon loading with HAuCl&lt;sub>4&lt;/sub>, the characteristics of the polymer templates govern the "loading sites" of the metal within the molecules. Unique morphologies were observed for the metal-loaded G0-G4 arborescent copolymers investigated, namely, spherical, toroidal, raspberry-like, spherical nanocage, and</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2025-04-25T18:05:55.835Z</modification><creation>2025-04-25T18:05:55.835Z</creation></dates><accession>S-EPMC9062874</accession><cross_references><pubmed>35516458</pubmed><doi>10.1021/acs.macromol.0c00778</doi></cross_references></HashMap>