Oxygenation of 1,5-cyclooctadiene (COD) is achieved on an iridium center using water as a reagent. A hydrogen-bonding interaction with an unbound nitrogen atom of the naphthyridine-based ligand architecture promotes nucleophilic attack of water to the metal-bound COD. Irida-oxetane and oxo-irida-allyl compounds are isolated, products which are normally accessed from reactions with H2O2 or O2. DFT studies support a ligand-assisted water activation mechanism.
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http://dx.doi.org/10.1021/jacs.5b03055 | DOI Listing |
Nano Lett
December 2024
Alan G. MacDiarmid Institute, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China.
Developing highly efficient non-iridium-based active sites for acidic water splitting is still a huge challenge. Herein, unique Ru-B-Cr moieties have been constructed in RuO nanofibers (NFs) to activate Ru sites for water electrolysis, which overcomes the bottleneck of RuO-based catalysts usually possessing low activity for the hydrogen evolution reaction (HER) and poor stability for the oxygen evolution reaction (OER). The fabricated Cr, B-doped RuO NFs exhibit low overpotentials of 205 and 379 mV for acidic HER and OER at 1 A cm with outstanding stability lasting 1000 and 188 h, respectively.
View Article and Find Full Text PDFChem Asian J
December 2024
CSIR - North East Institute of Science and Technology, Materials Sciences and Technology Division, Pulibor, CSIR-NEIST, 785006, Jorhat, INDIA.
Bimetallic catalysts have gained attention as promising contenders, owing to the synergistic interaction between two distinct metal centers. In this study, we present two N-heterocyclic carbene iridium(III) pentamethylcyclopentadienyl complexes [Cp*Ir(fcpyNHC)Cl]PF6 (1) and [Cp*Ir(pyNHC)Cl]PF6 (2) where 1 includes a ferrocene moiety acting as a bimetallic complex. Using ceric ammonium nitrate as a sacrificial oxidant, both complexes were tested for water oxidation.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
College of Chemistry and Materials Science, Hebei Research Center of the Basic Discipline of Synthetic Chemistry, Chemical Biology Key Laboratory of Hebei Province, Hebei University, Baoding 071002, PR China; Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, State Key Laboratory of New Pharmaceutical Preparations and Excipients, Baoding 071002, PR China. Electronic address:
Chem Sci
December 2024
Department of Chemistry, University of York Heslington YO10 5DD UK
This work details how the unusual iridium tetrahydride [Ir(H)(IMes)(sulfoxide)]Na and trihydride [Ir(H)(IMes)(sulfoxide)] can be formed in a solvent dependent reaction of [IrCl(COD)(IMes)] with sulfoxide (dimethyl or methylphenyl), base, and H. In the case of dimethyl sulfoxide, the four hydride ligands of the tetrahydride are equivalent, and the IMes and sulfoxide ligands mutually . However, for phenyl methyl sulfoxide, this isomer of the tetrahydride forms alongside its counterpart where the remarkable symmetry breaking effect of the sulfoxide leads to it presenting four chemically distinct hydride ligands.
View Article and Find Full Text PDFRSC Chem Biol
December 2024
Jiangsu Collaborative Innovation Center of Biomedical Functional Materials/Nanjing Drum Tower Hospital, College of Chemistry and Materials Science, Nanjing Normal University Nanjing 210023 China
Colon cancer is one of the most commonly diagnosed cancers and is recognized as the most aggressive tumor of the digestive system. Aberrant activation of signal transducer and activator of transcription 3 (STAT3) is associated with proliferation, metastasis and immunosuppression of the tumor cells. Here, to inhibit the STAT3 pathway and suppress metastasis in colon cancer cells, the half-sandwich iridium complex Ir-ART containing an artesunate-derived ligand was synthesized.
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