The photochemical reactivities of cobalt(III)-diamine and cobalt(III)-amino acid compounds have been compared using complexes that also contain polypyridyl ligands. Metallacyclic complexes result from UV-induced photodecarboxylation reactions of the amino acid complexes. UV-irradiation of closely related complexes with amine donors replacing the carboxylate donors does not lead to the production of the same metallacyclic products. The reported UV-induced fragmentation of amine donors and subsequent metallacycle formation appears not to be a general reaction. Nine cobalt(III) complexes of polypyridyl ligands have been structurally characterised, including four that also contain amino acid ligands and one that contains a three-membered metallacyclic ring.
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Molecules
January 2025
Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Campusvej 55, 5230 Odense M, Denmark.
The overexpression of the epidermal growth factor receptor (EGFR) in certain types of prostate cancers and glioblastoma makes it a promising target for targeted radioligand therapy. In this context, pairing an EGFR-targeting peptide with the emerging theranostic pair comprising the Auger electron emitter cobalt-58m (Co) and the Positron Emission Tomography-isotope cobalt-55 (Co) would be of great interest for creating novel radiopharmaceuticals for prostate cancer and glioblastoma theranostics. In this study, GE11 (YHWYGYTPQNVI) was investigated for its EGFR-targeting potential when conjugated using click chemistry to N1-((triazol-4-yl)methyl)-N1,N2,N2-tris(pyridin-2-ylmethyl)ethane-1,2-diamine (TZTPEN).
View Article and Find Full Text PDFSmall Methods
January 2025
Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh, 208016, India.
Molecular electronics exhibiting resistive-switching memory features hold great promise for the next generation of digital technology. In this work, electrosynthesis of ruthenium polypyridyl nanoscale oligomeric films is demonstrated on an indium tin oxide (ITO) electrode followed by an ITO top contact deposition yielding large-scale (junction area = 0.7 × 0.
View Article and Find Full Text PDFSensors (Basel)
December 2024
Chemical Optosensors & Applied Photochemistry Group (GSOLFA), Department of Organic Chemistry, Faculty of Chemistry, Complutense University of Madrid, 28040 Madrid, Spain.
Water conductivity sensing relies universally on electrical measurements, which are subject to corrosion of the electrodes and subsequent signal drift in prolonged in situ uses. Furthermore, they cannot provide contactless sensing or remote readout. To this end, a novel device for water conductivity monitoring has been developed by employing a microenvironment-sensitive ruthenium complex, [Ru(2,2'-bipyridine-4,4'-disulfonato)], embedded into a quaternary ammonium functionalized cross-linked polymer support.
View Article and Find Full Text PDFChemistry
December 2024
Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, 208016, Uttar Pradesh, India.
Herein, the photophysical, photochemical properties and photogenerated excited state dynamics of two new Ru(II) complexes, viz. [Ru(p-ttp)(bpy)(PTA)] [1], [Ru(p-ttp)(phen)(PTA)] [2] having a phosphorus-based ligand PTA [p-ttp=p-tolyl terpyridine; bpy=2,2'-bipyridyl; phen=1,10-phenanthroline and PTA=1,3,5-triaza-7-phosphaadamantane] are reported. Upon excitation with 470 nm LED, [1] and [2] neither undergo ligand release nor exhibit room temperature luminescence/O generation.
View Article and Find Full Text PDFInorg Chem
December 2024
School of Chemistry, University College Dublin, Dublin 4 D04 V1W8, Ireland.
The preparation, electrochemistry and photophysical properties of a heteroleptic chromium(III) polypyridyl complex [Cr(TMP)(dppn)] () containing two 3,4,7,8-tetramethyl-1,10-phenanthroline (TMP) ligands and the π-extended benzodipyrido[3,2-a:2',3'-]phenazine (dppn) ligand are reported. The visible absorption spectrum of reveals distinct bands between 320 and 420 nm characteristic of dppn-based ligand-centered transitions, with found to be nonemissive in aqueous solution but weakly luminescent in aerated acetonitrile solution. Transient visible absorption (TrA) spectroscopy reveals that 400 nm excitation of leads to initial population of a ligand-to-metal charge transfer (LMCT) state which evolves within tens of ps to form a dppn-localized intraligand (IL) state which persists for longer than 7 ns and efficiently sensitizes singlet oxygen.
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