Reduction of the pincer complex [OsCl(PNP)] (PNP = N(CHCHPtBu)) affords the isolation and full characterization of an osmium(ii) complex with square-planar coordination geometry, i.e. [OsCl(PNP)]. Spectroscopic, structural and magnetic data in combination with multireference computations indicate strong temperature independent paramagnetism, which arises from an energetically well separated ground state that mixes with excited states through spin-orbit coupling.
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http://dx.doi.org/10.1039/c7cc01569k | DOI Listing |
Molecules
October 2024
Department of Chemistry, University of the Free State, P.O. Box 339, Bloemfontein 9300, South Africa.
In coordination chemistry, 2,2':6',2″-terpyridine is a versatile and extensively studied tridentate ligand. Terpyridine forms stable complexes with a variety of metal ions through coordination sites provided by the three nitrogen atoms in its pyridine rings. This paper presents an electrochemical study on various bis(terpyridine)osmium(II) complexes, addressing the absence of a systematic investigation into their redox behavior.
View Article and Find Full Text PDFNanoscale
September 2024
School of Chemistry, University of Birmingham, Edgbaston, B15 2TT, UK.
Osmium(II) complexes have attractive properties for potential theranostic agents given their anticancer activitiy, their redox potentials favourable for biological transformations within cancer cells and their luminescence in the near infrared (NIR) region. To achieve localised detection and delivery, gold nanoparticles (AuNP) provide an attractive scaffold to attach multiple luminescent agents on a single particle and provide a multimodal platform for detection and loaclaised delivery. We have developed 13 nm and 25 nm AuNP decorated with an osmium complex based on 1,10-phenantholine and surface active bipyridine ligands, OsPhenSS for live cell imaging and singlet oxygen generation, notated as OsPhenSS·AuNP13 and OsPhenSS·AuNP25.
View Article and Find Full Text PDFMolecules
February 2024
Nano-Gene and Drug Delivery Group, Discipline of Biochemistry, School of Life Sciences, College of Agriculture, Engineering and Science, University of KwaZulu-Natal, Private Bag X54001, Durban 4000, South Africa.
A series of new chelating bidentate (SS) alkylimidazole-2-thione-Ru(II)/Os(II) complexes (, , , /, , ), and the tridentate (SNS) pyridine-2,6-diylimidazole-2-thione-Ru(II)/Os(II) complexes (, /, , ) in the forms [M(cym)(L)Cl]PF and [M(cym)(L)]PF (M = Ru or Os, cym = η--cymene, and L = heterocyclic derivatives of thiourea) respectively, were successfully synthesized. Spectroscopic and analytical methods were used to characterize the complexes and their ligands. Solid-state single-crystal X-ray diffraction analyses revealed a "piano-stool" geometry around the Ru(II) or Os(II) centers in the respective complexes.
View Article and Find Full Text PDFDalton Trans
March 2024
Institute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Straße 42, 1090 Vienna, Austria.
In this contribution we report the synthesis, characterization and anticancer activity of novel cyclometalated 4-phenylthiazole-derived ruthenium(II) (2a-e) and osmium(II) (3a-e) complexes. Formation and sufficient purity of the complexes were unambigiously confirmed by H-, C- and 2D-NMR techniques, X-ray diffractometry, HRMS and elemental analysis. The binding preferences of these cyclometalates to selected amino acids and to DNA models including G-quadruplex structures were analyzed.
View Article and Find Full Text PDFInorg Chem
December 2023
Department of Chemistry, Ramakrishna Mission Residential College (Autonomous), Narendrapur, Kolkata 700 103, India.
Herein, we disclose a unique method of oxidation of a 1,4-naphthoquinone ring in air. We report that (1,4-naphthoquinone)-NH-N=C(OH)Ph (HL) coordinated to octahedral ruthenium(II) and osmium(II) ions activates an O molecule spontaneously. Hydrogen atom transfer (HAT) from the -NH- function of HL to O and subsequent (2e + 2H) oxidation forming (1,3,4-trioxonaphthalen)=N-N=C(OH)Ph (HL) have been established.
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