<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang H</submitter><funding>Basic Energy Sciences</funding><funding>National Science Foundation</funding><pagination>20221-20226</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9650692</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>144(44)</volume><pubmed_abstract>Pore space partitioning (PSP) is methodically suited for dramatically increasing the density of guest binding sites, leading to the partitioned acs (pacs) platform capable of record-high uptake for CO&lt;sub>2&lt;/sub> and small hydrocarbons such as C&lt;sub>2&lt;/sub>H&lt;sub>&lt;i>x&lt;/i>&lt;/sub>. For gas separation, achieving high selectivity amid PSP-enabled high uptake offers an enticing prospect. Here we aim for high selectivity by introducing the bioisosteric (BIS) concept, a widely used drug design strategy, into the realm of pore-space-partitioned MOFs. New pacs materials have high C&lt;sub>2&lt;/sub>H&lt;sub>2&lt;/sub>/CO&lt;sub>2&lt;/sub> selectivity of up to 29, high C&lt;sub>2&lt;/sub>H&lt;sub>2&lt;/sub> uptake of up to 144 cm&lt;sup>3&lt;/sup>/g (298 K, 1 atm), and high separation potential of up to 5.3 mmol/g, leading to excellent </pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>Optimization of Pore-Space-Partitioned Metal-Organic Frameworks Using the Bioisosteric Concept.</pubmed_title><pmcid>PMC9650692</pmcid><funding_grant_id>2105961</funding_grant_id><funding_grant_id>2117040</funding_grant_id><funding_grant_id>DE-SC0010596</funding_grant_id><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Bu X</pubmed_authors><pubmed_authors>Hong AN</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Dang C</pubmed_authors><pubmed_authors>Feng P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of Pore-Space-Partitioned Metal-Organic Frameworks Using the Bioisosteric Concept.</name><description>Pore space partitioning (PSP) is methodically suited for dramatically increasing the density of guest binding sites, leading to the partitioned acs (pacs) platform capable of record-high uptake for CO&lt;sub>2&lt;/sub> and small hydrocarbons such as C&lt;sub>2&lt;/sub>H&lt;sub>&lt;i>x&lt;/i>&lt;/sub>. For gas separation, achieving high selectivity amid PSP-enabled high uptake offers an enticing prospect. Here we aim for high selectivity by introducing the bioisosteric (BIS) concept, a widely used drug design strategy, into the realm of pore-space-partitioned MOFs. New pacs materials have high C&lt;sub>2&lt;/sub>H&lt;sub>2&lt;/sub>/CO&lt;sub>2&lt;/sub> selectivity of up to 29, high C&lt;sub>2&lt;/sub>H&lt;sub>2&lt;/sub> uptake of up to 144 cm&lt;sup>3&lt;/sup>/g (298 K, 1 atm), and high separation potential of up to 5.3 mmol/g, leading to excellent </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T09:02:37.773Z</modification><creation>2025-04-04T09:02:37.773Z</creation></dates><accession>S-EPMC9650692</accession><cross_references><pubmed>36305830</pubmed><doi>10.1021/jacs.2c09349</doi></cross_references></HashMap>