<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(10)</volume><submitter>Sutradhar M</submitter><funding>Fundação para a Ciência e a Tecnologia, Portugal</funding><pubmed_abstract>Bis(2-hydroxybenzylidene)isophthalohydrazide (H?L) has been used to synthesize the dinuclear [Cu?(1?&lt;i>NO&lt;/i>²:2?&lt;i>N'O'&lt;/i>²-H?L)(NO?)?(H?O)?] (&lt;b>1&lt;/b>) and the tetranuclear [Cu?(?-1?&lt;i>NO&lt;/i>²:2?&lt;i>N&lt;/i>&lt;i>'O&lt;/i>²-H?L)?(?-NO?)?(H?O)?]·2C?H?OH (&lt;b>2&lt;/b>) complexes. The solvent plays an important role in determining the ligand behaviour in the syntheses of the complexes. An ethanol-acetonitrile mixture of solvents favours partials enolization in the case of &lt;b>2&lt;/b>. Both complexes have been characterized by elemental analysis, infrared radiation (IR), single crystal X-ray crystallography and electrochemical methods. The variable temperature magnetic susceptibility measurements of &lt;b>2&lt;/b> show strong antiferromagnetic coupling between the central nitrato-bridged Cu (II) ions. The catalytic activity of both &lt;b>1&lt;/b> and &lt;b>2&lt;/b> has been screened toward the solvent-free microwave-assisted oxidation of alcohols and the peroxidative oxidation of alkanes under mild conditions. Complex &lt;b>1&lt;/b> exhibits the highest activity for both oxidation reactions, leading selectively to a maximum product yield of 99% (for the 1-phenylethanol oxidation after 1 h without any additive) and 13% (for the cyclohexane oxidation to cyclohexyl hydroperoxide, cyclohexanol and cyclohexanone after 3 h).</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6222479</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Peroxidative Oxidation of Alkanes and Alcohols under Mild Conditions by Di- and Tetranuclear Copper (II) Complexes of Bis (2-Hydroxybenzylidene) Isophthalohydrazide.</pubmed_title><pmcid>PMC6222479</pmcid><funding_grant_id>UID/QUI/00100/2013, PTDC/QEQ-ERQ/1648/2014, PTDC/QEQ-QIN/3967/2014 and SFRH/BPD/86067/2012</funding_grant_id><pubmed_authors>Sutradhar M</pubmed_authors><pubmed_authors>Guedes da Silva MFC</pubmed_authors><pubmed_authors>Alegria ECBA</pubmed_authors><pubmed_authors>Pombeiro AJL</pubmed_authors><pubmed_authors>Liu CM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Peroxidative Oxidation of Alkanes and Alcohols under Mild Conditions by Di- and Tetranuclear Copper (II) Complexes of Bis (2-Hydroxybenzylidene) Isophthalohydrazide.</name><description>Bis(2-hydroxybenzylidene)isophthalohydrazide (H?L) has been used to synthesize the dinuclear [Cu?(1?&lt;i>NO&lt;/i>²:2?&lt;i>N'O'&lt;/i>²-H?L)(NO?)?(H?O)?] (&lt;b>1&lt;/b>) and the tetranuclear [Cu?(?-1?&lt;i>NO&lt;/i>²:2?&lt;i>N&lt;/i>&lt;i>'O&lt;/i>²-H?L)?(?-NO?)?(H?O)?]·2C?H?OH (&lt;b>2&lt;/b>) complexes. The solvent plays an important role in determining the ligand behaviour in the syntheses of the complexes. An ethanol-acetonitrile mixture of solvents favours partials enolization in the case of &lt;b>2&lt;/b>. Both complexes have been characterized by elemental analysis, infrared radiation (IR), single crystal X-ray crystallography and electrochemical methods. The variable temperature magnetic susceptibility measurements of &lt;b>2&lt;/b> show strong antiferromagnetic coupling between the central nitrato-bridged Cu (II) ions. The catalytic activity of both &lt;b>1&lt;/b> and &lt;b>2&lt;/b> has been screened toward the solvent-free microwave-assisted oxidation of alcohols and the peroxidative oxidation of alkanes under mild conditions. Complex &lt;b>1&lt;/b> exhibits the highest activity for both oxidation reactions, leading selectively to a maximum product yield of 99% (for the 1-phenylethanol oxidation after 1 h without any additive) and 13% (for the cyclohexane oxidation to cyclohexyl hydroperoxide, cyclohexanol and cyclohexanone after 3 h).</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2021-02-21T08:14:34Z</modification><creation>2019-03-27T00:06:52Z</creation></dates><accession>S-EPMC6222479</accession><cross_references><pubmed>30347723</pubmed><doi>10.3390/molecules23102699</doi></cross_references></HashMap>