<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Y</submitter><funding>NCI NIH HHS</funding><pagination>12041-12044</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6203447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(85)</volume><pubmed_abstract>Four distinct fluorescent states are achieved in a single Weak-Link Approach (WLA) construct bearing pyrene and tetraphenylethene moieties. The fluorescence of the compound in both the solution and solid phases can be manipulated through reversible coordination chemistry at the PtII center.</pubmed_abstract><journal>Chemical communications (Cambridge, England)</journal><pubmed_title>A four-state fluorescent molecular switch.</pubmed_title><pmcid>PMC6203447</pmcid><funding_grant_id>U54 CA199091</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Mirkin CA</pubmed_authors><pubmed_authors>Xing H</pubmed_authors><pubmed_authors>Wasielewski MR</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A four-state fluorescent molecular switch.</name><description>Four distinct fluorescent states are achieved in a single Weak-Link Approach (WLA) construct bearing pyrene and tetraphenylethene moieties. The fluorescence of the compound in both the solution and solid phases can be manipulated through reversible coordination chemistry at the PtII center.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2020-10-29T14:42:45Z</modification><creation>2019-11-05T08:04:04Z</creation></dates><accession>S-EPMC6203447</accession><cross_references><pubmed>30294737</pubmed><doi>10.1039/c8cc05159c</doi></cross_references></HashMap>