<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(16)</volume><submitter>Heydarian S</submitter><funding>Ilam University</funding><funding>Islamic Azad University</funding><pubmed_abstract>The surface of boehmite nanoparticles (γ-AlOOH NPs) consists of hydroxy groups that enable their surface modification and functionalization. Based on this fact, we first functionalized the AlOOH NP surface with a Schiff-base ligand in this work. The Schiff-base ligand was synthesized from the reaction of &lt;i>o&lt;/i>-formylphenol and (3,4-diaminophenyl)(phenyl)methanone. Then, palladium nanoparticles were immobilized on it, denoted as Pd@boehmite. Next, Pd@boehmite was investigated using TGA, DSC, SEM, TEM, and BET instrumental methods. Then, Pd@boehmite was used as a powerful catalyst for carbon-carbon bond formation in the Suzuki coupling reaction. Various aryl halide and aryl boronic acid derivatives were investigated using the Pd@boehmite nanocatalyst and all biphenyl products were obtaine</pubmed_abstract><journal>Nanoscale advances</journal><pagination>4867-4875</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12208136</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A new palladium complex Schiff-base on functionalized nanoboehmite as a reusable and practical catalyst for selective Suzuki C-C bond formation.</pubmed_title><pmcid>PMC12208136</pmcid><pubmed_authors>Heydarian S</pubmed_authors><pubmed_authors>Darabi M</pubmed_authors><pubmed_authors>Tahmasbi B</pubmed_authors></additional><is_claimable>false</is_claimable><name>A new palladium complex Schiff-base on functionalized nanoboehmite as a reusable and practical catalyst for selective Suzuki C-C bond formation.</name><description>The surface of boehmite nanoparticles (γ-AlOOH NPs) consists of hydroxy groups that enable their surface modification and functionalization. Based on this fact, we first functionalized the AlOOH NP surface with a Schiff-base ligand in this work. The Schiff-base ligand was synthesized from the reaction of &lt;i>o&lt;/i>-formylphenol and (3,4-diaminophenyl)(phenyl)methanone. Then, palladium nanoparticles were immobilized on it, denoted as Pd@boehmite. Next, Pd@boehmite was investigated using TGA, DSC, SEM, TEM, and BET instrumental methods. Then, Pd@boehmite was used as a powerful catalyst for carbon-carbon bond formation in the Suzuki coupling reaction. Various aryl halide and aryl boronic acid derivatives were investigated using the Pd@boehmite nanocatalyst and all biphenyl products were obtaine</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-03-31T11:49:39.793Z</modification><creation>2025-09-01T03:06:15.539Z</creation></dates><accession>S-EPMC12208136</accession><cross_references><pubmed>40599371</pubmed><doi>10.1039/d5na00362h</doi></cross_references></HashMap>