<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lo W</submitter><funding>NIGMS NIH HHS</funding><pagination>9883-92</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3483649</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(18)</volume><pubmed_abstract>The formation and solution properties, including stability in mixed aqueous-Me(2)SO media, have been investigated for an [Fe(4)S(4)](2+) cluster derived from β-cyclodextrin (CD) dithiolate. Clusters of the type [Fe(4)S(4)(SAr)(4)](2-) (Ar = Ph, C(6)H(4)-3-F) are generated in Me(2)SO by redox reactions of [Fe(4)S(4)(SEt)(4)](2-) with 2 equiv of ArSSAr. An analogous reaction with the intramolecular disulfide of 6(A),6(D)-(3-NHCOC(6)H(4)-1-SH)(2)-6(A),6(D)-dideoxy-β-cyclodextrin (14), whose synthesis is described, affords a completely substituted cluster formulated as [Fe(4)S(4){β-CD-(1,3-NHCOC(6)H(4)S)(2)}(2)](2-) (15). Ligand binding is indicated by a circular dichroism spectrum and also by UV-visible and isotropically shifted (1)H NMR spectra and redox behavior convincingly similar to [Fe(</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>Formation, spectroscopic characterization, and solution stability of an [Fe4S4]2+ cluster derived from β-cyclodextrin dithiolate.</pubmed_title><pmcid>PMC3483649</pmcid><funding_grant_id>R37 GM028856</funding_grant_id><funding_grant_id>GM28856</funding_grant_id><funding_grant_id>R01 GM028856</funding_grant_id><pubmed_authors>Holm RH</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Ling CC</pubmed_authors><pubmed_authors>Lo W</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Formation, spectroscopic characterization, and solution stability of an [Fe4S4]2+ cluster derived from β-cyclodextrin dithiolate.</name><description>The formation and solution properties, including stability in mixed aqueous-Me(2)SO media, have been investigated for an [Fe(4)S(4)](2+) cluster derived from β-cyclodextrin (CD) dithiolate. Clusters of the type [Fe(4)S(4)(SAr)(4)](2-) (Ar = Ph, C(6)H(4)-3-F) are generated in Me(2)SO by redox reactions of [Fe(4)S(4)(SEt)(4)](2-) with 2 equiv of ArSSAr. An analogous reaction with the intramolecular disulfide of 6(A),6(D)-(3-NHCOC(6)H(4)-1-SH)(2)-6(A),6(D)-dideoxy-β-cyclodextrin (14), whose synthesis is described, affords a completely substituted cluster formulated as [Fe(4)S(4){β-CD-(1,3-NHCOC(6)H(4)S)(2)}(2)](2-) (15). Ligand binding is indicated by a circular dichroism spectrum and also by UV-visible and isotropically shifted (1)H NMR spectra and redox behavior convincingly similar to [Fe(</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Sep</publication><modification>2025-04-05T12:54:51.263Z</modification><creation>2019-03-27T00:59:39Z</creation></dates><accession>S-EPMC3483649</accession><cross_references><pubmed>22934734</pubmed><doi>10.1021/ic301324u</doi></cross_references></HashMap>