<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>5(16)</volume><submitter>Ishida J</submitter><pubmed_abstract>Herein, the synthesis of new N,N-dimethylformamide (DMF)-protected palladium nanoparticles (Pd NPs-OAc) employing Pd (OAc)2 (= Pd(OCOCH3)2) as the NP precursor is reported. Pd NPs-OAc were comprehensively characterized by transmission electron microscopy, FT-IR, NMR, and X-ray photoelectron spectroscopy to determine the Pd NP size distribution and the coordination state of DMF. Pd NPs-OAc were compared with Pd NPs-Cl, using PdCl2 as the NP precursor. The Suzuki-Miyaura cross-coupling reaction proceeded efficiently in the presence of Pd NPs-OAc and a high catalytic activity was observed with a turnover number of up to 1.5 × 105. Furthermore, the Pd NP-OAc catalysts could be recycled at least five times.</pubmed_abstract><journal>ACS omega</journal><pagination>9598-9604</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7191860</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and Characterization of N,N-Dimethylformamide-Protected Palladium Nanoparticles and Their Use in the Suzuki-Miyaura Cross-Coupling Reaction.</pubmed_title><pmcid>PMC7191860</pmcid><pubmed_authors>Ishida J</pubmed_authors><pubmed_authors>Suzuki T</pubmed_authors><pubmed_authors>Kawasaki H</pubmed_authors><pubmed_authors>Nagata T</pubmed_authors><pubmed_authors>Nakatsuji M</pubmed_authors><pubmed_authors>Obora Y</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Synthesis and Characterization of N,N-Dimethylformamide-Protected Palladium Nanoparticles and Their Use in the Suzuki-Miyaura Cross-Coupling Reaction.</name><description>Herein, the synthesis of new N,N-dimethylformamide (DMF)-protected palladium nanoparticles (Pd NPs-OAc) employing Pd (OAc)2 (= Pd(OCOCH3)2) as the NP precursor is reported. Pd NPs-OAc were comprehensively characterized by transmission electron microscopy, FT-IR, NMR, and X-ray photoelectron spectroscopy to determine the Pd NP size distribution and the coordination state of DMF. Pd NPs-OAc were compared with Pd NPs-Cl, using PdCl2 as the NP precursor. The Suzuki-Miyaura cross-coupling reaction proceeded efficiently in the presence of Pd NPs-OAc and a high catalytic activity was observed with a turnover number of up to 1.5 × 105. Furthermore, the Pd NP-OAc catalysts could be recycled at least five times.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2020-05-22T19:32:11Z</modification><creation>2020-05-22T19:32:11Z</creation></dates><accession>S-EPMC7191860</accession><cross_references><pubmed>32363312</pubmed><doi>10.1021/acsomega.0c01006 </doi></cross_references></HashMap>