The first example of a hexadecanuclear copper(II) phosphonate containing pyrazole, hydroxide and acetate ancillary ligands has been assembled in a reaction involving copper(II) nitrate, pyrazole, t-butylphosphonic acid and triethylamine.
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http://dx.doi.org/10.1039/b905456a | DOI Listing |
J Phys Chem Lett
December 2022
U.S. Army Combat Capabilities Development Command Chemical Biological Center, 8198 Blackhawk Road, Aberdeen Proving Ground, Maryland 21010, United States.
Organophosphonates were originally developed as insecticides but were quickly identified as highly toxic acetylcholinesterase inhibitors, leading to their exploitation as chemical warfare agents (CWA). To develop next generation filtration technologies, there must be a fundamental understanding of the molecular interactions occurring with toxic chemicals, such as CWAs. In this paper, we investigate the interaction between dry CuO nanoparticles and sarin (GB), using infrared (IR) spectroscopy in an effort to build an atomic understanding.
View Article and Find Full Text PDFInorg Chem
February 2021
Univ. Brest, UMR CNRS 6521, 6 Avenue Victor Le Gorgeu, 29200 Brest, France.
Herein we present the preparation of two novel cyclam-based macrocycles ( and ), bearing phosphonate-appended pyridine side arms for the coordination of copper(II) ions in the context of Cu PET imaging. The two ligands have been prepared through conventional protection-alkylation sequences on cyclam, and their coordination properties have been thoroughly investigated. The corresponding copper complexes have been fully characterized in the solid state (X-ray diffraction analysis) and in solution (EPR and UV-vis spectroscopies).
View Article and Find Full Text PDFDalton Trans
March 2020
Department of Chemistry, Indiana University Northwest, Gary, Indiana 46408, USA.
The synthesis of a heteromacrocyclic bifunctional chelator with phosphonic acid pendent arms is presented along copper(ii) complexation. Ligand NS-POH featuring N,N'-bis-substituted phosphonate pendent arms was isolated in respectable yields, characterized, and chelated to copper(ii). Implementation of both Moedritzer-Irani and Kabachnik-Fields conditions using aza-thia macrocycle 1,8-dithia-4,11-diazacyclotetradecane afforded 1,8-dithia-4,11-diazacyclotetradecane-4,11-diyl-bis-(methylene)-bis-(phosphonic acid) (NS-POH).
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
December 2018
ICMUB, UMR CNRS 6302, Université Bourgogne Franche-Comté, 9 avenue Alain Savary, 21078 Dijon cedex, France.
In the title compound, [Cu(OH){CHN(POCH)}(HO)]·7HO, two Cu cations are bridged by two hydroxide groups, forming a centrosymmetric binuclear complex. Each Cucation is further coordinated by the N atoms of a bidentate ethyl (1,10-phenanthrolin-3-yl)phospho-nate anion and a water mol-ecule in a square-pyramidal geometry. In the crystal, a network of O-H⋯O hydrogen bonds involving the P(O)(O)(OEt) groups, bridging hydroxyl groups, coordinated and uncoordinated water mol-ecules generates a three-dimensional supra-molecular structure.
View Article and Find Full Text PDFChem Commun (Camb)
June 2018
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210023, P. R. China.
The reaction of copper(ii) chloride with 2-carboxyphenylphosphonic acid (2-cppH3) under hydrothermal conditions at 100 °C results in the formation of a polar compound, Cu3(2-cpp)2(H2O)5 (1), which shows large dielectric anisotropy. A similar reaction at 140 °C results in a centrosymmetric phase, Cu3(2-cpp)2(H2O)2 (2). Compound 1 can convert into 2 upon increasing the reaction temperature under hydrothermal conditions, and further to Cu3(2-cpp)2 (3) upon thermal treatment at 240 °C.
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