Six dinuclear lanthanide(III) nitrato complexes [Ln(NO)(HO)](-tppz) (where tppz = 2,3,5,6-tetra(2-pyridyl) pyrazine and Ln(III) = Nd (), Sm (), Eu (), Gd (), Tb (), and Dy ()) with bis-tridentate N-heterocyclic 2,3,5,6-tetra(2-pyridyl)pyrazine as bridging ligand have been solvothermally synthesized and characterized via elemental analysis, infrared spectroscopy, thermogravimetric analysis, single-crystal X-ray diffraction, and powder X-ray diffraction. The 3-D Hirshfeld surface and 2-D fingerprint plots show that the main interactions in - are the O⋯H/H⋯O intermolecular interactions with relative contributions of about 62%. Although the poor lanthanide(III)-centered luminescence properties clearly point to the efficiency of nonradiative quenching processes (presence of water molecules in the coordination sphere of the lanthanide(III) ions), the ligand tppz is better suited to sensitize the lanthanide(III)'s emissions of Eu and Nd than Sm, Tb, and Dy. Finally, the magnetic data of Dy comple× reveals antiferromagnetic coupling between Dy ions.
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http://dx.doi.org/10.1016/j.jlumin.2020.117835 | DOI Listing |
J Am Chem Soc
November 2024
Department of Chemistry, University of Fribourg, Chemin du Musée 9, 1700 Fribourg, Switzerland.
-selective ring-opening metathesis polymerization (ROMP) with the commercial Grubbs "nitrato catalyst" has shown promise for synthesizing stereoregular materials, but it comes with the drawback of losing control over the molecular weight due to the poor initiation rate of the catalyst and the need for stoichiometric ruthenium complex loading. To address these issues, we developed a chain transfer polymerization method that allows for the catalytic synthesis of polymers while controlling the degree of polymerization. This allowed us to produce shorter polymers with exceptional chain-end control.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
August 2024
Phosphorus Laboratory Department of Chemistry Indian Institute of Technology, Bombay,Mumbai 400076 India.
Reaction of thorium(IV) nitrate with 2-[(4-phenyl-1-1,2,3-triazol-1-yl)meth-yl]pyridine () yielded (H)[Th(NO)] or (CHN)[Th(NO)] (), instead of the expected mixed-ligand complex [Th(NO) ], which was detected in the mass spectrum of . In the structure, the [Th(NO)] anions display an icosa-hedral coordination geometry and are connected by H cations through C-H⋯O hydrogen bonds. The H cations inter-act N-H⋯N hydrogen bonds.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
June 2024
L. V. Pisarzhevskii Institute of Physical Chemistry of the National Academy of Sciences of Ukraine, Prospect Nauki 31, Kyiv, 03028, Ukraine.
J Inorg Biochem
September 2024
Department of Chemical Physiology and Biochemistry, School of Medicine, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, USA. Electronic address:
The NO dioxygenation reaction catalyzed by heme-containing globin proteins is a crucial aerobic detoxification pathway. Accordingly, the second order reaction of NO with oxymyoglobin and oxyhemoglobin has been the focus of a large number of kinetic and spectroscopic studies. Stopped-flow and rapid-freeze-quench (RFQ) measurements have provided evidence for the formation of a Fe(III)-nitrato complex with millisecond lifetime prior to release of the nitrate product, but the temporal resolution of these techniques is insufficient for the characterization of precursor species.
View Article and Find Full Text PDFChemMedChem
August 2024
Institute of Inorganic Chemistry, RWTH Aachen University, Aachen, Germany.
Cobalt complexes exhibit versatile reactivity with nitric oxide (NO), enabling their utilization in applications ranging from homogeneous catalysis to NO-based modulation of biological processes. However, the coordination geometry around the cobalt center is complex, the therapeutic window of NO is narrow, and controlled NO delivery is difficult. To better understand the complexation of cobalt with NO, we prepared four cobalt nitrato complexes and present a structure-property relationship for ultrasound-triggerable NO release.
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