<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(6)</volume><submitter>Rodriguez-Florez LV</submitter><pubmed_abstract>Multilayer graphene (MLG), obtained by mild sonication of graphite in NMP, was functionalised &lt;i>via&lt;/i> 1,3-dipolar cycloaddition with azomethine ylides generated by thermal 1,2-prototropy from various imino esters. The microwave-assisted functionalisation took place in five hours at 100 °C. The resulting MLG, containing substituted proline-based amine functional groups, was characterized using XPS and showed a nitrogen loading three times that obtained for the same transformation performed for five days using convection-assisted heating. The preparation of the imino ester containing a bipyridine unit at the arylidene position allowed for the preparation of the corresponding functionalised MLG, which incorporated the ruthenium atom to achieve a heterogeneous MLG-Ru complex. This supported complex was tested, as a proof of concept, as a photocatalyst of the aerobic oxidative hydroxylation of 4-methoxyphenylboronic acid.</pubmed_abstract><journal>Nanoscale advances</journal><pagination>1648-1652</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10929589</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preparation of a ruthenium complex covalently bonded to multilayer graphene and its evaluation as a photocatalyst.</pubmed_title><pmcid>PMC10929589</pmcid><pubmed_authors>Navlani-Garcia M</pubmed_authors><pubmed_authors>Rodriguez-Florez LV</pubmed_authors><pubmed_authors>Sansano JM</pubmed_authors><pubmed_authors>Yus M</pubmed_authors><pubmed_authors>Cazorla-Amoros D</pubmed_authors><pubmed_authors>Najera C</pubmed_authors><pubmed_authors>de Gracia Retamosa M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preparation of a ruthenium complex covalently bonded to multilayer graphene and its evaluation as a photocatalyst.</name><description>Multilayer graphene (MLG), obtained by mild sonication of graphite in NMP, was functionalised &lt;i>via&lt;/i> 1,3-dipolar cycloaddition with azomethine ylides generated by thermal 1,2-prototropy from various imino esters. The microwave-assisted functionalisation took place in five hours at 100 °C. The resulting MLG, containing substituted proline-based amine functional groups, was characterized using XPS and showed a nitrogen loading three times that obtained for the same transformation performed for five days using convection-assisted heating. The preparation of the imino ester containing a bipyridine unit at the arylidene position allowed for the preparation of the corresponding functionalised MLG, which incorporated the ruthenium atom to achieve a heterogeneous MLG-Ru complex. This supported complex was tested, as a proof of concept, as a photocatalyst of the aerobic oxidative hydroxylation of 4-methoxyphenylboronic acid.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2024-11-07T11:30:21.487Z</modification><creation>2024-11-07T11:30:21.487Z</creation></dates><accession>S-EPMC10929589</accession><cross_references><pubmed>38482040</pubmed><doi>10.1039/d4na00075g</doi></cross_references></HashMap>