RESUMEN

Ti6Al4V alloy is the most commonly employed implant material for orthopedic replacements due to its good mechanical properties close to those of bones, biocompatibility and its good corrosion resistance in biological media. Nevertheless, it does not exhibit good wear resistance, showing friction and wear even with soft tissues. This latter feature can lead to a premature failure of the implant with the subsequent component replacement. Therefore, a system with good tribological resistance is required for several medical applications. One possible alternative to solve tribological problems consists of protecting the alloy surface by means of biocompatible Ti-C-N coatings. In this work, five types of metallic Ti-C-N coatings deposited by physical vapor deposition (PVD) cathodic arc method on Ti6Al4V substrate have been studied. Different deposition conditions have been analyzed, and the superficial properties of films have been characterized. Additionally, tribological response of these films have been determined and compared with the substrate one under fretting conditions in simulated body fluid. The results indicate that Ti-C-N coatings improve the general response of the biomaterial.

Asunto(s)

Aleaciones/química , Materiales Biocompatibles Revestidos/química , Titanio/química , Ensayo de Materiales , Prótesis e Implantes , Espectrometría Raman , Propiedades de Superficie , Difracción de Rayos X

RESUMEN

Four compounds of general formula [M(4,4'bipy)(N(3))2](n) (M = Mn (1), Zn (2), Co (3), Ni (4)) have been synthesized and magnetostructurally characterized by means of X-ray diffraction analysis, IR and ESR spectroscopies, and measurements of the magnetic susceptibility and magnetization. Compound 1 (C(10)H(8)N(8)Mn) crystallizes in the tetragonal P4(3)2(1)2 space group, Z = 4, with a = 8.229(2), b = 8.229(2), and c = 16.915(2) A. It exhibits an acentric 3D structure where Mn(II) ions are linked through EE-azide groups resulting in a diamondoid network. The 4,4'bipy ligands are coordinated on the axial positions of the octahedral spheres reinforcing the intermetallic connections. Weak ferromagnetism arising from spin canting is observed for compound 1. Compounds 2, 3, and 4 are proposed to be isomorphous and would consist of a 2D array where alternating EO + EE/EO + EE/EO + EO azide-chains are linked by 4,4'bipy ligands resulting in pi-pi stacked pyridyl-columns. The azido ligand dispositions in compounds 3 and 4 make possible systems of type -AF-AF-F-, which would give rise to a topological ferromagnetic behavior.

RESUMEN

Three tetrameric cobalt(II)-pseudohalide complexes have been structurally and magnetically characterized. Compounds 1 and 2 are isomorphous and exhibit the general formula [Co2(dpk-OH)(dpk-CH3O)(L)(H2O)]2A2-4H2O where dpk = di-2-pyridyl ketone, L = N3(-) and A = BF4(-) for 1, and L = NCO(-) and A = ClO4(-) for 2. The ligands dpk-OH(-) and dpk-CH3O(-) result from solvolysis and ulterior deprotonation of dpk in water and methanol, respectively. Both compounds exhibit cationic tetramers consisting of a dicubane-like core with two missing vertexes where the Co(II) ions are connected through end-on pseudohalide and oxo-bridges. A similar tetranuclear core has been found for 3 whose formula is [Co2(dpk-OH)(dpk-CH3O)(NCO)2]2. In this case, the tetramers are neutral and exhibit a terminal cyanate in place of the coordinated molecule of water for 1 and 2. The tetrameric units for 2 and 3 represent the first examples of any kind of cubanes exhibiting cyanate bridges as well as the first Co(II) compounds exhibiting intermetallic bridges through these pseudohalide groups. Measurements of the magnetic susceptibility indicated the presence of ferromagnetic Co(II)-Co(II) interactions in the three compounds.

RESUMEN

Compounds [Mn(dca)2bipym] (1), [Cu2(dca)4bipym] (2), and [Mn2(dca)4bipym] (3) have been synthesized and structural (2, 3) and magnetically characterized. Compound 1 is isomorphous with [Mn(dca)2bipy]. Compound 2 crystallizes in the monoclinic P2(1)/c space group, Z = 4, with a = 7.5609(9), b = 11.477(42), and c = 11.792(2) A and beta = 106.565(6) degrees. Compound 3 crystallizes in the monoclinic system, space group P2(1)/n, with a = 7.396(3) A, b = 11.498(7) A, and c = 12.349(9) A and beta = 106.61(5) degrees. While compound 1 is one-dimensional, with the manganese(II) ions bridged by double mu1,5-dicyanamide ligands, the structural arrangement in compounds 2 and 3 is three-dimensional based on ladder-like moieties. These units, whose steps are bipym groups, extend through mu1,5-dca bridges and are connected to another four on the plane perpendicular to the extension of the ladders to form the 3D arrangement. Magnetic susceptibility measurements show antiferromagnetic couplings in all cases, increasing for 1, 3, and 2, respectively.