RESUMEN
Veterinary anti-inflammatory Cu(II) complexes of indomethacin (1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid = IndoH), of the general formula [Cu(2)(Indo)(4)L(2)] (L = N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), N-methylpyrrolidone (NMP), and water), were studied by zero-field and X-band EPR spectroscopies, electronic spectroscopy, magnetic measurements, and X-ray powder diffraction. The complexes are similar to Cu(II) acetate monohydrate, with a strong antiferromagnetic exchange interaction, J, ranging from -141 to -152 cm(-)(1). Variable temperature magnetic susceptibility data for all of the complexes are similar, with the exception of a [Cu(2)(Indo)(4)(H(2)O)(2)] complex, which displays an unusual increase in magnetic moment with decreasing temperature from 50 to 10 K. The X-ray powder diffraction patterns of the DMF and DMA dimers show that they are isostructural. Two isostructural H(2)O complexes were synthesized from different methods yet displayed different variable temperature magnetic susceptibity data. All of the [Cu(2)(Indo)(4)L(2)] complexes crystallize in the triclinic space group P&onemacr;. Single-crystal X-ray diffraction analysis of the DMF complex, [Cu(2)(Indo)(4)(DMF)(2)].1.6(DMF), shows that it is similar to the previously reported [Cu(2)(Indo)(4)(DMSO)(2)] with a Cu-Cu bond length of 2.630(1) Å, Cu-O(RCOO) of 1.960(4)-1.967(4) Å, and Cu-O(DMF) of 2.143(5) Å and crystal parameters a = 10.848(3) Å, b = 13.336(6) Å, c = 16.457(4) Å, alpha = 104.67(3) degrees, beta = 100.94(2) degrees, and gamma = 107.16(3) degrees. The X-ray structure of the DMF dimer does not exhibit strong intermolecular interactions due to the hydrophobic nature of the exterior. This may be important in facilitating its dissolution in micelles and transport through membranes.
RESUMEN
The stability of the peroxide ligand bridging two manganese ions in the trinuclear oxomanganese complex [Mn(III)(3)(mu(3)-O)(mu-O(2))(AcO)(2)(dien)(3)](2+), one of only two structurally characterized Mn clusters possessing a mu(1,2)-peroxo bridge, has been investigated using density functional theory. Although the peroxide O-O bond in the related bis(mu-oxo)-bridged complex [Mn(IV)(2)(mu-O)(2)(mu-O(2))(NH(3))(6)](2+) undergoes spontaneous cleavage upon two-electron reduction to the Mn(III)(2) dimer, calculations on the model complexes [Mn(III)(2)(mu-O)(mu-O(2))(NH(3))(8)](2+) and [Mn(III)(2)(mu-O)(mu-O(2))(NH(3))(6)(H(2)O)(2)](2+), which contain the same mu-oxo-,mu-peroxo-bridged core present in the trimer, indicate that the peroxide bridge remains intact, in agreement with experiment. Its stability can be attributed to a Jahn-Teller distortion resulting in elongation of the axial Mn-N bonds perpendicular to the Mn(2)(mu-O)(mu-O(2)) plane which in turn stabilizes the high-spin Mn(III) oxidation state. However, the difference in the energies of the bridged and cleaved peroxide structures is small (ca. 0.5 eV), the lowest energy structure depending on the nature of the terminal ligands. Calculations on the model trimer complex [Mn(III)(3)(mu(3)-O)(mu-O(2))(HCO(2))(2)(NH(3))(9)](2+) indicate that the energetic differences between the cleaved and uncleaved structures is even smaller (ca. 0.2 eV), and although the peroxo-bridge remains more or less intact, it is likely to be quite facile.
RESUMEN
Numerous reports describe the photoluminescence of two- and three-coordinate gold(I)-phosphine complexes, but emission in their analogous four-coordinate complexes is almost unknown. This work examines the luminescence of tetrahedral gold(I) complexes of the types [Au(diphos)(2)]PF(6) (diphos = 1,2-bis(diphenylphosphino)ethane, 1) and [Au(2)(tetraphos)(2)](PF(6))(2) (tetraphos = (R,R)-(+/-)/(R,S)-1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane, (R,R)-(+/-)/(R,S)-2). Although nonemitting in solution, these complexes luminesce with an intense yellow color (lambda(max) 580-620 nm) at 293 K in the solid state or when immobilized as molecular dispersions within solid matrixes. The excited-state lifetimes of the emissions (tau 4.1-9.4 micros) are markedly dependent on the inter- and intramolecular phenyl-phenyl pairing interactions present. At 77 K in an ethanol glass, two transitions are observed: a minor emission at lambda(max) 415-450 nm and a major emission at lambda(max) 520-595 nm. For [Au(1)(2)]PF(6), lifetimes of tau 251.0 +/- 20.5 micros were determined for the former transition and tau 14.9 +/- 4.6 micros for the latter. Density functional theory (DFT) calculations and comparative studies indicate that the former of these emissions involves triplet LMCT pi(Ph) --> Au(d)-P(p) transitions associated with individual P-phenyl groups. The latter emissions, which are the only ones observed at 293 K, are assigned to LMCT pi(Ph-Ph) --> Au(d)-P(p) transitions associated with excited P-phenyl dimers. Other tetrahedral gold(I)-phosphine complexes containing paired P-Ph substituents display similar emissions. The corresponding phosphine ligands, whether free, protonated, or bound to Ag(I), do not exhibit comparable emissions. Far from being rare, luminescence in four-coordinate Au(I)-phosphine complexes appears to be general when stacked P-phenyl groups are present.