<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tan L</submitter><funding>European Research Council</funding><funding>Stockholms Universitet (Stockholm University)</funding><funding>Vetenskapsrådet (Swedish Research Council)</funding><funding>Beijing Institute of Technology (BIT)</funding><funding>Verband der Chemischen Industrie (Chemical Industry Association)</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>1471</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8933400</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>The construction of hierarchically nanoporous composite for high-performance catalytic application is still challenging. In this work, a series of host-in-host ionic porous materials are crafted by encapsulating ionic organic cages into a hyper-crosslinked, oppositely charged porous poly(ionic liquid) (PoPIL) through an ion pair-directed assembly strategy. Specifically, the cationic cage (C-Cage) as the inner host can spatially accommodate a functional Au cluster, forming a [Au⊂C-Cage&lt;sup>+&lt;/sup>]⊂PoPIL&lt;sup&gt;-&lt;/sup> supramolecular composite. This dual-host molecular hierarchy enables a charge-selective substrate sorting effect to the Au clusters, which amplifies their catalytic activity by at least one order of magnitude as compared to Au confined only by C-Cage as the mono-host (Au⊂C-Cage&lt;sup>+&lt;/sup>). Moreover, we demonstrate that such dual-host porous system can advantageously immobilize electrostatically repulsive Au⊂C-Cage&lt;sup>+&lt;/sup> and cationic ferrocene co-catalyst (Fer&lt;sup>+&lt;/sup>) together into the same microcompartments, and synergistically speed up the enzyme-like tandem reactions by channelling the substrate to the catalytic centers via nanoconfinement.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Electrostatically cooperative host-in-host of metal cluster ⊂ ionic organic cages in nanopores for enhanced catalysis.</pubmed_title><pmcid>PMC8933400</pmcid><funding_grant_id>NAPOLI-639720</funding_grant_id><funding_grant_id>SU FV-2.1.1-005</funding_grant_id><funding_grant_id>639720</funding_grant_id><funding_grant_id>22071008</funding_grant_id><funding_grant_id>2018-05351</funding_grant_id><funding_grant_id>Dozentenpreis 15126</funding_grant_id><funding_grant_id>52003029</funding_grant_id><funding_grant_id>3100011181910</funding_grant_id><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Zhou JH</pubmed_authors><pubmed_authors>Sun JK</pubmed_authors><pubmed_authors>Yuan J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrostatically cooperative host-in-host of metal cluster ⊂ ionic organic cages in nanopores for enhanced catalysis.</name><description>The construction of hierarchically nanoporous composite for high-performance catalytic application is still challenging. In this work, a series of host-in-host ionic porous materials are crafted by encapsulating ionic organic cages into a hyper-crosslinked, oppositely charged porous poly(ionic liquid) (PoPIL) through an ion pair-directed assembly strategy. Specifically, the cationic cage (C-Cage) as the inner host can spatially accommodate a functional Au cluster, forming a [Au⊂C-Cage&lt;sup>+&lt;/sup>]⊂PoPIL&lt;sup&gt;-&lt;/sup> supramolecular composite. This dual-host molecular hierarchy enables a charge-selective substrate sorting effect to the Au clusters, which amplifies their catalytic activity by at least one order of magnitude as compared to Au confined only by C-Cage as the mono-host (Au⊂C-Cage&lt;sup>+&lt;/sup>). Moreover, we demonstrate that such dual-host porous system can advantageously immobilize electrostatically repulsive Au⊂C-Cage&lt;sup>+&lt;/sup> and cationic ferrocene co-catalyst (Fer&lt;sup>+&lt;/sup>) together into the same microcompartments, and synergistically speed up the enzyme-like tandem reactions by channelling the substrate to the catalytic centers via nanoconfinement.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-05-29T21:53:02.33Z</modification><creation>2025-05-29T21:53:02.33Z</creation></dates><accession>S-EPMC8933400</accession><cross_references><pubmed>35304468</pubmed><doi>10.1038/s41467-022-29031-y</doi></cross_references></HashMap>