5 research outputs found
1D and 3D supramolecular structures exhibiting weak ferromagnetism in three Cu(II) complexes based on malonato and di-alkyl-2,2’-bipyridines
Abstract Manganese coordination polymers {Mn(- fum)(5dmb)(H2O)2}n (1) and {[Mn2(fum)2(4dmb)2] H2O}n (2) (fum= fumarato; 5dmb = 5,50-dimethyl-2,20-bipyridine; 4dmb = 4,40-dimethyl-2,20-bipyridine) were obtained from one-pot, solution reactions under ambient conditions. The fum ligand acquires different coordination modes in the presence of the different dmb ancillary ligands, promoting distinctive crystal structures, including divergent dimensionalities. Thus, X-ray single-crystal data reveal that complex 1 crystallizes in a monoclinic system with C2/c space group and forms an infinite one-dimensional polymer. The Mn(II) center is six-coordinated and displays a distorted octahedral configuration. In addition, the solid-state selfassembly of the polymeric structure of 1 gives rise to a twodimensional (2D) supramolecular framework, mainly through hydrogen bonding. In contrast, complex 2 crystallizes in a monoclinic system with a Cc space group and forms an infinite 2D coordination polymer having dinuclear units. The Mn(II) center has a distorted octahedral configuration. The thermal stabilities of both coordination polymers were investigated. Variable-temperature magnetic measurements show that complex 1 is paramagnetic, while complex 2 exhibits weak antiferromagnetic coupling between adjacent Mn(II) centers.supported by CONACyT project 129293, DGAPA-UNAM project IN106014, and ICYTDF, project PICCO
Synthesis and characterization of nanometric magnetite coated by oleic acid and the surfactant CTAB
For the intermediate and largest particles a mixture of magnetite and maghemite phases were produced as the saturation magnetization values of MS ∼ 60 emu/g indicated; these values were measured for most samples, independently of the coating surfactant concentration, and according to the ZFC-FC curves the blocking temperatures were 225K and 275K for the smallest and largest magnetite nanoparticles, respectively. The synthesis method was highly reproducible.Nanometric magnetite (nm-Fe3O4) particles were prepared by the reverse co-precipitation synthesis method, obtaining particle sizes that ranged from 4 to 8.5 nm. In their synthesis, the concentration of iron salts of ferric nitrate, Fe(NO3)3⋅9H2O, and ferrous sulfate, FeSO4⋅7H2O, were varied relative to the chemical reaction volume and by using different surfactants such as oleic acid (OA) and hexadecyltrimethylammonium bromide (CTAB). The nm-Fe3O4 particles were characterized by transmission electron microscopy (TEM), Mössbauer spectroscopy (MS), magnetic and X-ray diffraction (XRD) measurements
1,4-Cyclohexanedicarboxylato-bridged cobalt coordination polymers: Synthesis, crystal structures and magnetic properties
1,4-Cyclohexanedicarboxylato-bridged cobalt coordination polymers:
Synthesis, crystal structures and magnetic propertiesThree coordination polymers have been synthesized, using self-assembly solution reactions at ambient
conditions, combining Co(II) ion with 1,4-ciclohexanedicarboxylic acid, in the presence of 1,10-phenantrolione
and two different 2,20-bipyridines, as co-ligands: [Co(H2O)(cdc)(phen)]n (1); {[Co(H2O)(cdc)(4dmb)]
2H2O}n (2); {[Co(H2O)(cdc)(5dmb)] 3H2O}n (3), where cdc = e,a-cis-1,4-ciclohexanedicarboxylato,
phen = 1,10-phenantroline, 4dmb = 4,40-dimethyl-2,20-bipyridine, and 5dmb = 5,50-dimethyl-2,20-bipyridine.
Crystallographic studies show that these compounds have one-dimensional (1D) structures; Co(II)
in 1–3 is six-coordinated with a distorted-octahedral coordination sphere. Complexes 2 and 3 exhibit a
novel bridging motif of the cdc ligand in its equatorial, axial cis configuration. In addition, the solid-state
self-assembly of the polymeric structure of 1 gives rise to a 2D supramolecular framework, mainly through
hydrogen bonding. In contrast, complex 2 forms an infinite 1D supramolecular array, made of double Co
ion rows bridged by hydrogen bonding interactions. Complex 3 generates an intricate 2D supramolecular
framework also throughout hydrogen bonding. The thermal stabilities of the three coordination polymers
were investigated. Magnetic properties measurements reveal that complexes 1–3 exhibit weak antiferromagnetic
ordering with h(C-W) = 9.6, 5.8 and 7.5 K, and E2 = 0.51, 0.16 and 0.28 cm 1, accordingly to
Curie-Weiss model and Rueff phenomenological approach, respectively
Modification of the structure and magnetic properties of fumarato-bridged Mn coordination polymers through different dimethyl-2,20-bipyridine co-ligands
Abstract Manganese coordination polymers {Mn(- fum)(5dmb)(H2O)2}n (1) and {[Mn2(fum)2(4dmb)2] H2O}n (2) (fum= fumarato; 5dmb = 5,50-dimethyl-2,20-bipyridine; 4dmb = 4,40-dimethyl-2,20-bipyridine) were obtained from one-pot, solution reactions under ambient conditions. The fum ligand acquires different coordination modes in the presence of the different dmb ancillary ligands, promoting distinctive crystal structures, including divergent dimensionalities. Thus, X-ray single-crystal data reveal that complex 1 crystallizes in a monoclinic system with C2/c space group and forms an infinite one-dimensional polymer. The Mn(II) center is six-coordinated and displays a distorted octahedral configuration. In addition, the solid-state selfassembly of the polymeric structure of 1 gives rise to a twodimensional (2D) supramolecular framework, mainly through hydrogen bonding. In contrast, complex 2 crystallizes in a monoclinic system with a Cc space group and forms an infinite 2D coordination polymer having dinuclear units. The Mn(II) center has a distorted octahedral configuration. The thermal stabilities of both coordination polymers were investigated. Variable-temperature magnetic measurements show that complex 1 is paramagnetic, while complex 2 exhibits weak antiferromagnetic coupling between adjacent Mn(II) centers.supported by CONACyT project 129293, DGAPA-UNAM project IN106014, and ICYTDF, project PICCO. R.E
Muconato-bridged Mn coordination polymer exhibiting rare distorted-trigonal prismatic coordination geometry
Muconato-bridged Manganese Coordination Polymer exhibiting rare Distorted-trigonal Prismatic Coordination ArrangementNovel poly[Mn(H2O)(dmb)(muco)] (1) (H2muco = trans,trans-muconic acid; dmb = 5,5 -dimethyl-2,2 -bipyridine) was obtained by self-assembly, one-pot, solution reaction. 1 crystallizes in a monoclinic system with P21 space group and forms an infinite onedimensional (1D) polymer. Remarkably, the six-coordinate MnII display a rare distorted trigonal prismatic configuration. This unusual co-ordination arrangement appears to be acquired due to the supramolecular interactions of the polymeric structure of 1, mainly throughout hydrogen bonding, giving rise to a 2D framework. Magnetic properties measurements reveal that 1 possesses weak antiferromagnetic interactions with θ(C–W) = –1.0 K and J = 458 cm–1