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Su, Esra; Guven, Alaettin; Kani, Ibrahim
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"> <dc:creator>Su, Esra</dc:creator> <dc:creator>Guven, Alaettin</dc:creator> <dc:creator>Kani, Ibrahim</dc:creator> <dc:date>2018-01-01</dc:date> <dc:description>Two new homobinuclear manganese compounds with mixed ligands, [Mn-2((1,1)-2-NH2C6H4COO)(2)(phen)(4)](ClO4)2(CH3OH) (1), and [Mn-2((1,3)-2-NH2C6H4COO)(2)(bipy)(4)](ClO4)2 (2) (NH2C6H4COOH=anthranilic acid, bipy=2,2-bipyridine, phen=1,10- phenanthroline) were synthesized and thoroughly characterized by elemental analysis, IR, UV and single crystal X-ray crystallography. X-ray structure analysis shows that in the mono- and bidentate carboxylate bridged compounds, Mn-Mn distances of 1 and 2 are 3,461 angstrom, and 4,639 angstrom, respectively. The energy of the compounds was determined with a DFT (Density Functional Theory) calculation on B3LYP/6-31G(d,p) optimized geometry by using the B3LYP/6-31G(d,p) basis set. These compounds acts as biomimetic catalyst and show catalase-like activity for the hydrogen peroxide dismutation at room temperature in different solvents with remarkable activity (TOF, Turnover frequency=mol of subst./(mol of cat. x time)) up to 12640h(-1) with 1, and 17910h(-1) with 2 in Tris-HCl buffer). Moreover, the catalytic activity of 1 and 2 has been studied for oxidation of alcohols (cinnamyl alcohol, benzyl alcohol, cyclohexanol, 1-octanol and 1-heptanol) and alkenes (cyclohexene, styrene, ethyl benzene, 1-octene and 1-hexene) in a homogeneous catalytic system consisting t-butylhydroperoxide (TBHP) as an oxidant in acetonitrile. Both compounds exhibited very high activity in the oxidation of cyclohexene to cyclohexanone (similar to 80% selectivity, similar to 99% conversion in 1h, TOF=243h(-1) and 226h(-1)) and cinnamyl alcohol to cinnamaldehyde (similar to 64% selectivity) as the main product with very high TOF value (9180h(-1) and 13040h(-1) in the first minute of reaction) (similar to 100% conversion in 0.5h) with TBHP at 70 degrees C in acetonitrile, for 1 and 2, respectively.</dc:description> <dc:identifier>https://aperta.ulakbim.gov.trrecord/29063</dc:identifier> <dc:identifier>oai:zenodo.org:29063</dc:identifier> <dc:rights>info:eu-repo/semantics/openAccess</dc:rights> <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights> <dc:source>APPLIED ORGANOMETALLIC CHEMISTRY 32(2)</dc:source> <dc:title>Oxygen bridged Homobinuclear Mn(II) compounds with Anthranilic acid: Theoretical calculations, oxidation and catalase activity</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> <dc:type>publication-article</dc:type> </oai_dc:dc>
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