Hexafluoroacetylacetonates that contain lead and divalent first-row transition metals, PbM(hfac)(4) (M = Ni (1), Co (2), Mn (3), Fe (4), and Zn (5)), have been synthesized. Their heterometallic structures are held together by strong Lewis acid-base interactions between metal atoms and diketonate ligands acting in chelating-bridging fashion. Compounds 1-5 are highly volatile and decompose below 350 °C. Fluorinated heterometallic β-diketonates have been used for the first time as volatile single-source precursors for the preparation of mixed-metal fluorides. Complex fluorides of composition Pb(2)MF(6) have been obtained by decomposition of 1-5 in a two-zone furnace under low-pressure nitrogen flow. Lead-transition metal fluorides conform to orthorhombically distorted Aurivillius-type structure with layers of corner-sharing [MF(6)] octahedra separated by α-PbO-type (Pb(2)F(2)) blocks. Pb(2)NiF(6) and Pb(2)CoF(6) were found to exhibit magnetic ordering below 80 and 43 K, respectively. The ordering is antiferromagnetic, with a weak, uncompensated moment due to the canting of spins. The Pb(2)MF(6) fluorides represent a new class of prospective magnetoelectric materials combining transition metals and lone-pair main-group cations.
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http://dx.doi.org/10.1021/ja109128r | DOI Listing |
Molecules
November 2022
Postovsky Institute of Organic Synthesis, The Ural Branch of the Russian Academy of Sciences, Ekaterinburg 620108, Russia.
This review summarizes the data on the synthesis of coordination compounds containing two or more different metal ions based on fluorinated β-diketonates. Heterometallic systems are of high interest in terms of their potential use in catalysis, medicine and diagnostics, as well as in the development of effective sensor devices and functional materials. Having a rich history in coordination chemistry, fluorinated β-diketones are well-known ligands generating a wide variety of heterometallic complexes.
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November 2021
Laboratoire de Tectonique Moléculaire, UMR Université de Strasbourg-CNRS 7140, icFRC, Université de Strasbourg, F-67000 Strasbourg, France.
Seven isostructural heterometallic luminescent (Ir,Cd) coordination polymers were prepared upon the combination of tris-chelate cationic Ir(III) complexes behaving as metalloligands with Cd(II) salts. Three octahedral Ir(III) complexes have been considered in the present report. They consist of a bipyridine unit functionalised with 3-pyridyl moieties as peripheral coordinating sites and two 2-phenylpyridyl cyclometalating derivatives.
View Article and Find Full Text PDFChem Sci
July 2020
Department of Chemistry, Molecular Sciences Research Hub, Imperial College London 80 Wood Lane, Shepherds Bush London W12 0BZ UK
A palladium pre-catalyst, [Pd(PCy)] is reported for the efficient and selective C-F alumination of fluorobenzenes with the aluminium(i) reagent [{(ArNCMe)CH}Al] (, Ar = 2,6-di-iso-propylphenyl). The catalytic protocol results in the transformation of sp C-F bonds to sp C-Al bonds and provides a route to reactive organoaluminium complexes () from fluorocarbons. The catalyst is highly active.
View Article and Find Full Text PDFMolecules
November 2018
Departamento de Química Orgánica y Química Inorgánica, Instituto de Investigacion en Química "Andres M. del Río" (IQAR) Universidad de Alcalá, Campus Universitario, 28871-Alcala de Henares, Madrid, Spain.
New heterometallic aluminium-alkali metal compounds have been prepared using Schiff bases with electron withdrawing substituents as ligands. The synthesis of these new species was achieved via the reaction of AlMe₃ with the freshly prepared alkali-metallated ligand. The derivatives formed were characterized by NMR in solution and by single crystal X-ray diffraction in the solid state.
View Article and Find Full Text PDFChempluschem
November 2016
State Key Laboratory of Fluorine and Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute, Xi'an, 710065, China.
3-Oxy-furoxanate is immobilized in a heterometallic energetic metal-organic framework (MOFs). Two furoxan-based MOFs ([Ag K (BDOFO)(BDFO) (H O) ] , [K (BDFO)] ) and a salt ([(BDFO )(NH NH ) (H O)] (BDOFO =4,5-bis(dinitromethyl)-3-oxy-furoxanate, BDFO =4,5-bis(dinitromethyl)-furoxanate) are synthesized and their energetic performance evaluated. This study outlines the systematic investigation of detonation performance of 3-oxy-furoxan and its derivatives.
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