PubMed Health⌕ Search

Biomedical subjects

Youkoh Kaizu

Publications and source records attributed to Youkoh Kaizu.

7 recordsLinked to original sources

Static magnetic-field-induced phase lag in the magnetization response of tris(dipicolinato)lanthanides.

Alternating-current (ac) magnetic susceptibility measurements for tris(dipicolinato) complexes with a trivalent heavy lanthanide ion, [N(C2H5)4]3[Ln(dipic)(3)] x nH2O (dipic = pyridine-2,6-dicarboxylate; Ln = Tb, Dy, Ho, Er, Tm, or Yb) are reported. While none of the six complexes showed a magnetization lag from the ac magnetic field of 10-10(3) Hz above 1.8 K, the Dy, Er, and Yb complexes with odd numbers of 4f electrons exhibited the magnetization lag in a static magnetic field. This phenomenon is explained to be caused by the elimination of a fast relaxation path, which is only effective for the Kramers doublet ground states in near zero field. At higher static fields, the remaining paths such as Orbach and/or direct processes govern the dynamics of the two-level systems comprised of spin-up and spin-down states. The non-Kramers complexes were found to have a nondegenerate ground state with large energy gaps from higher states, which is consistent with their fast magnetization relaxation.

Journal Article↗

Upward temperature shift of the intrinsic phase lag of the magnetization of Bis(phthalocyaninato)terbium by ligand oxidation creating an S = 1/2 spin.

An alternating-current (ac) magnetic susceptibility measurement for the [(Pc)(2)Tb(III)](0) complex (Pc = phthalocyaninato) has shown that ligand oxidation of the anionic [(Pc)(2)Tb(III)](-) complex gives rise to a significant upward shift of the temperature range where the magnetization response shows a phase lag behind the time-varying external magnetic field. The peaks of the out-of-phase component of the ac susceptibility of the pi-radical [(Pc)(2)Tb(III)](0) were observed at 50, 43, and 36 K with ac magnetic fields of 10(3), 10(2), and 10 Hz, respectively, which were more than 10 K higher than the corresponding values of the anionic complex with a closed-shell pi-system. The ac susceptibility measurements on the complex with octa(dodecoxy)-substituted Pc ligand, which is readily dilutable in diamagnetic media, proved that the significant rise of the temperatures occurs as an intrinsic single-molecular property of the complex possessing both J = 6 and S = (1)/(2) systems, and is not due to long-range magnetic order or interactions between adjacent unpaired pi-electrons.

Ligands↗

Lanthanide double-decker complexes functioning as magnets at the single-molecular level.

Double-decker phthalocyanine complexes with Tb3+ or Dy3+ showed slow magnetization relaxation as a single-molecular property. The temperature ranges in which the behavior was observed were far higher than that of the transition-metal-cluster single-molecule magnets (SMMs). The significant temperature rise results from a mechanism in the relaxation process different from that in the transition-metal-cluster SMMs. The effective energy barrier for reversal of the magnetic moment is determined by the ligand field around a lanthanide ion, which gives the lowest degenerate substate a large |Jz| value and large energy separations from the rest of the substates in the ground-state multiplets.

Journal Article↗

Determination of ligand-field parameters and f-electronic structures of double-decker bis(phthalocyaninato)lanthanide complexes.

The f-electronic structures of the ground states of anionic bis(phthalocyaninato)lanthanides, [Pc(2)Ln](-) (Pc = dianion of phthalocyanine, Ln = Tb(3+), Dy(3+), Ho(3+), Er(3+), Tm(3+), or Yb(3+)), are determined. Magnetic susceptibilities of the powder samples of [Pc(2)Ln]TBA (TBA = tetra-n-butylammonium cation) in the range 1.8-300 K showed characteristic temperature dependences which resulted from splittings of the ground-state multiplets. NMR signals for the two kinds of protons on the Pc rings at room temperature were shifted to lower frequency with respect to the diamagnetic Y complex in Ln = Tb, Dy, and Ho cases, and to higher frequency in Er, Tm, and Yb cases. The ratios of the paramagnetic shifts of the two positions were near constant in the six cases. This indicates that the shifts are predominantly caused by the magnetic dipolar term, which is determined by the anisotropy of the magnetic susceptibility of the lanthanide ion. Using a multidimensional nonlinear minimization algorithm, we determined a set of ligand-field parameters that reproduces both the NMR and the magnetic susceptibility data of the six complexes simultaneously. Each ligand-field parameter was assumed to be a linear function of atomic number of the lanthanide. The energies and wave functions of the sublevels of the multiplets are presented. Temperature dependences of anisotropies in the magnetic susceptibilities are theoretically predicted for the six complexes.

Journal Article↗

Interaction between f-electronic systems in dinuclear lanthanide complexes with phthalocyanines.

The first detection and characterization of the interactions between the f-electronic systems in the dinuclear complexes of paramagnetic trivalent Tb, Dy, Ho, Er, Tm, and Yb ions with phthalocyanine ligands are presented. The molar magnetic susceptibilities, chi(m), were measured for PcLnPcLnPc* ([Ln, Ln]; Pc = dianion of phthalocyanine, Pc* = dianion of 2,3,9,10,16,17,23,24-octabutoxyphthalocyanine) and PcLnPcYPc* ([Ln, Y]) in the range from 1.8 K to room temperature. The selective synthetic method previously reported for the heterodinuclear complex [Y, Ln] was used to prepare [Ln, Ln] and [Ln, Y] with a modification on the choice of starting materials. The f-f interaction contributions to the magnetic susceptibility are evaluated as Delta(chi)(m)T = chi(m)([Ln, Ln])T - chi(m)([Ln, Y])T - chi(m)([Y, Ln])T, where T refers to temperature on the kelvin scale. The homodinuclear complexes having f(8)-f(10)-systems, namely [Tb, Tb], [Dy, Dy], and [Ho, Ho], show positive Delta(chi)(m)T values in the 1.8-50 K range, indicating the existence of ferromagnetic interaction between the f-systems. The magnitude of the Delta(chi)(m)T increases in the descending order of the number of f-electrons. [Er, Er] gives negative Delta(chi)(m)T values in the 1.8-50 K range, showing the antiferromagnetic nature of the f-f interaction. [Tm, Tm] exhibits small and negative Delta(chi)(m)T values, which gradually decline in the negative direction as the temperature decreases in the range 13-50 K and sharply rise in the positive direction as the temperature falls from 10 to 1.8 K. [Yb, Yb] has extremely small Delta(chi)(m)T values, whose magnitude at 2 K is less than 1% of that of [Tb, Tb]. The ligand field parameters of the ground-state multiplets of the six [Ln, Y] complexes are determined by simultaneous fitting to both the magnetic susceptibility data and paramagnetic shifts of (1)H NMR. The theoretical analysis successfully converged by assuming that each ligand field parameter is a function of the number of f-electrons in each ion. Using these parameters as well as the previously obtained corresponding parameters for the [Y, Ln] series, the interactions between the f-systems in [Ln, Ln] are investigated. All the characteristic observations above are satisfactorily reproduced with the assumption that the magnetic dipolar term is the sole source of the f-f interaction.

Journal Article↗

Crystal Structure and Energy Transfer in Double-Complex Salts Composed of Tris(2,2'-bipyridine)ruthenium(II) or Tris(2,2'-bipyridine)osmium(II) and Hexacyanochromate(III).

In crystals of double-complex salts [M(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O (M(2+) = Ru(2+), Os(2+); bpy = 2,2'-bipyridine), luminescence from (3)CT state of [M(bpy)(3)](2+) is partially quenched by [Cr(CN)(6)](3)(-) at 77 K and room temperature (RT). This quenching is attributed to intermolecular excitation energy transfer from the (3)CT state of [M(bpy)(3)](2+) to the (2)E(g) state of [Cr(CN)(6)](3)(-). Crystal structure and crystal parameters of [Os(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O: monoclinic, C2, a = 22.384(4) Å, b = 13.827(4) Å, c = 22.186(3) Å, beta = 90.70(2) degrees, V = 6866(2) Å(3), Z = 4, R = 0.0789, R(w) = 0.1932: are almost the same as those of [Ru(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O: monoclinic, C2, a = 22.414(2) Å, b = 13.7686(15) Å, c = 22.207(2) Å, beta = 90.713(8) degrees, V = 6852.9(12) Å(3), Z = 4, R = 0.0554, R(w) = 0.1679. Moreover, these double complex salts have the same distance and relative orientation between donor and acceptor. The rate of intermolecular energy transfer from [M(bpy)(3)](2+) to [Cr(CN)(6)](3)(-) was evaluated by the decay time of luminescence from (3)CT state of [M(bpy)(3)](2+) in single- and double-complex salts. The rate of energy transfer in [Os(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O (4.9 x 10(7) s(-)(1)) is about eight times larger than that in [Ru(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O (6.0 x 10(6) s(-)(1)) at 77 K. The difference of energy transfer rate is brought about by only the spectral overlap between the normalized luminescence spectrum from the (3)CT state of donor ([M(bpy)(3)](2+)) and the normalized excitation spectrum of the (2)E(g) state of acceptor ([Cr(CN)(6)](3)(-)) in the salts. Decay rates of the (3)CT state in [M(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O were measured as a function of temperature. A large enhancement of a decay rate from the (3)CT state was obtained for [Ru(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O as the temperature was increased. This result implies that an additional path from the (3)CT state of [Ru(bpy)(3)](2+) to the (2)T(2g) state of [Cr(CN)(6)](3)(-) would be opened for energy transfer with a rise in temperature in [Ru(bpy)(3)](2)[Cr(CN)(6)]Cl.8H(2)O.

Journal Article↗