We report the synthesis, crystal structures, and magnetic properties of two new metal-radical chains built up from a new class of organic radical-based ligands, the polychlorinated triphenylmethyl (PTM) radicals. Crystal structures of two new 1D coordination polymers, [Cu(2)(PTMDC)(2)(py)(5)(EtOH)].3EtOH (1) and [Co(2)(PTMDC)(2)(DMF)(2)(H(2)O)(6)].5DMF (2) (where PTMDC is a PTM radical functionalized with two carboxylic groups), show similar chain-like structures, in which each of the PTMDC radicals are connecting two Cu(II) or Co(II) metal ions. Therefore, from a magnetic point of view, both structures describe a magnetic chain model based on the PTMDC-M(II) unit. In this manuscript, the magnetic exchange coupling constants between both metal ions and the bridging PTM radicals have been determined. In both cases, the temperature dependence of the magnetic susceptibility reveals antiferromagnetic exchange coupling constants between the PTMDC radicals and Cu(II) (J/k(B) = -42 K) and Co(II) (J/k(B) = -14.6 K) ions based on the exchange Hamiltonian H = -J sum S(A(i))S(A(i+1)).
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Dalton Trans
August 2021
Department of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
The preparation, crystal structures, and magnetic properties of a family of hetero-tri-spin 1-D coordination polymers with the formula [Ln(hfac)Cu(hfac)(4-NIT-MePyz)] (Ln = Gd, 1, Tb, 2, Dy, 3; hfac = hexafluoroacetylacetonate; 4-NIT-MePyz = 2-{4-(1-methyl)-pyrazolyl}-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) are reported. In these complexes, the 4-NIT-MePyz radical acts as a linker to bridge the Cu and Ln ions through its pyrazole and aminoxyl groups to form a chain structure. Magnetic properties typical of spin-chains are observed for Dy and Tb derivatives but single-chain magnet (SCM) behavior was evidenced only for the Tb compound which is characterized by an energy gap for demagnetization / of 31 K.
View Article and Find Full Text PDFJ Am Chem Soc
May 2018
Department of Chemistry , Northwestern University, Evanston , Illinois 60208-3313 , United States.
We report the synthesis of a semiquinoid-bridged single-chain magnet, as generated through a thermally induced metal-ligand electron transfer. Reaction of FeCl with 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone (LH) in the presence of (NMe)Cl gave the compound (NMe)[LFeCl]. Together, variable-temperature X-ray diffraction, Mössbauer spectra, Raman spectra, and dc magnetic susceptibility reveal a transition from a chain containing (L)Fe units to one with (L)Fe upon decreasing temperature, with a transition temperature of T = 213 K.
View Article and Find Full Text PDFACS Omega
March 2018
Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.
Two stable nitronyl nitroxide free radicals { = 4'-methoxy-phenyl-4,4,5,5,-tetramethylimidazoline-1-oxyl-3-oxide (NNPhOMe) and = 2-(2'-thienyl)-4,4,5,5-tetramethylimidazoline 3-oxide 1-oxyl (NNT)} are successfully synthesized using Ullmann condensation. The reactions of these two radicals with 3d transition metal ions, in the form of M(hfac) (where M = Co or Mn, hfac: hexafluoroacetylacetone), result in four metal-organic complexes Co(hfac)(NNPhOMe), ; Co(hfac)(NNT)·(HO), ; Mn(hfac)(NNPhOMe)·(CH), ; and Mn(hfac)(NNT), . The crystal structure and magnetic properties of these complexes are investigated by single-crystal X-ray diffraction, dc magnetization, infrared, and electron paramagnetic resonance spectroscopies.
View Article and Find Full Text PDFInorg Chem
October 2015
Instituto de Química, Universidade Federal Fluminense , Niterói, 24020-150, Rio de Janeiro, Brazil.
Two isostructural 1D complexes, [M(hfac)2NaphNN]n [M = Mn(II) (1) or Co(II) (2); NaphNN = 1-naphthyl nitronylnitroxide], were synthesized and exhibit very strong antiferromagnetic metal-radical exchange coupling. Compound 2 shows slow magnetic relaxation behavior with a high blocking temperature (TB ≈ 13.2 K) and a very high coercive field of 49 kOe at 4.
View Article and Find Full Text PDFChemistry
October 2014
Department of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry, Tianjin Key Laboratory of Metal and Molecule-based Material Chemistry and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071 (China).
Employing nitronyl nitroxide lanthanide(III) complexes as metallo-ligands allowed the efficient and highly selective preparation of three series of unprecedented hetero-tri-spin (Cu-Ln-radical) one-dimensional compounds. These 2p-3d-4f spin systems, namely [Ln3Cu(hfac)11(NitPhOAll)4] (Ln(III) = Gd 1Gd, Tb 1Tb, Dy 1Dy; NitPhOAll = 2-(4'-allyloxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide), [Ln3Cu(hfac)11(NitPhOPr)4] (Ln(III) = Gd 2Gd, Tb 2Tb, Dy 2Dy, Ho 2Ho, Yb 2Yb; NitPhOPr = 2-(4'-propoxyphenyl)-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxide) and [Ln3Cu(hfac)11(NitPhOBz)4] (Ln(III) = Gd 3Gd, Tb 3Tb, Dy 3Dy; NitPhOBz=2-(4'-benzyloxyphenyl)-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxide) involve O-bound nitronyl nitroxide radicals as bridging ligands in chain structures with a [Cu-Nit-Ln-Nit-Ln-Nit-Ln-Nit] repeating unit. The dc magnetic studies show that ferromagnetic metal-radical interactions take place in these hetero-tri-spin chain complexes, these and the next-neighbor interactions have been quantified for the Gd derivatives.
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