Stereoselective synthesis of the C14-C24 degraded fragment of symbiodinolide

Symbiodinolide is a polyol macrolide isolated from the marine dinoflagellate Symbiodinium sp. in 2007. The C14-C24 fragment of symbiodinolide possessing the 17R/18R/21R absolute configuration, which was obtained as one of the degraded products of symbiodinolide, was synthesized stereoselectively from cis-2-butene-1,4-diol. The detailed comparison of the synthetic product with the degraded product in the spectroscopic data confirmed that the stereostructure of the C14-C24 fragment was 17R, 18R, and 21R.     

Grubbs carbene complex-catalyzed cleavage of allyl vic-diols to aldehydes with a co-oxidant: application to the selective cleavage of huge marine molecules

An oxidative cleavage of allyl vic-diols to aldehydes catalyzed by a Grubbs carbene complex using a co-oxidant has been established for the first time, with good yields. The utility of this selective cleavage reaction was demonstrated through the use of two huge marine molecules, symbiodinolide and N-p-BrBz palytoxin.     

Generation of 12-fs pulses from a diode-pumped Kerr-lens mode-locked Cr:LiSAF laser

We demonstrate 12-fs-pulse generation from a diode-pumped Kerr-lens mode-locked Cr:LiSAF laser. This is to our knowledge the shortest pulse ever produced from a mode-locked Cr:LiSAF laser. Based on an improved estimation of the intracavity dispersions, we utilized BK7 glass for the Brewster-prism-pair material.     

Carbon-13 NMR studies of the biologically active nor-diterpenoid dilactones from Podocarpus plants

Carbon-13 NMR signals of the biologically active norditerpenoid dilactones from Podocarpus plants were fully assigned by using selective ¹H decoupling, coupling constants (²J_CH), spin-lattice relaxation times (T₁) and correlation of the spectra of more than thirty dilactone congeners. The spectra of five nagilactones, B, C, D, E and F, which constitute representative members of three major structural types of the dilactones: (A) 8:14, 9:11-dienolide (α-pyrone) type, (B) 7α:8α-epoxy-9:11-enolide type, and (C) 7:8,9:11-dienolide type, were extensively analysed. Some characteristic steric interactions for the substituents on the ring system can be demonstrated from the spectral properties.     

Theory of the spin depolarisation rate of μ+ SR in pure Fe

The diffusion constant (D) and the spin depolarisation rate (λ_S) of the positive muon in the ferromagnetic b.c.c. lattices such as Fe have been calculated on the basis of the small polaron (SP) model with particular attention to the hopping and the coherent motions. They have been obtained in the forms: $\text{D=}\text{d}{}^2\text{w}{}_{\mathrm{D}}\text{6}$ and $\text{λ}{}_{\mathrm{S}}\text{=}\text{4γ}{}^2{}_{\mathrm{\mu }}\text{H}{}^2{}_{\mathrm{d}}\text{3w}{}_{\mathrm{S}}$, where d is a jump length, and H_d is a magnitude of internal dipolar field. At high temperatures, the activated-type hopping motion gives a dominant contribution to w_D, and w_S coincides with w_D. With decreasing temperature, w_D turns to be increasing owing to the coherent motion. Whereas w_S deviates from w_D, after passing the minimum, to have a maximum, and then decreases in inverse proportion to a lifetime (_B) of the SP band states. Because of the cell periodicity of the internal fields, the spin in an SP band state feels a definite magnetic field corresponding to the state, and sees various fields if scattered to other states. These scattering processes succeeding in a time shorter than (γ_μH_d)^-1 result in the motional narrowing of the spectra, with λ_{S ?} γ²_μH_d_B.     

Muon spin relaxation studies of magnetic-field-induced effects in high-Tc superconductors

Muon spin relaxation measurements in high transverse magnetic fields [FORMULA: SEE TEXT] revealed strong field-induced quasistatic magnetism in the underdoped and Eu-doped (La,Sr)2CuO4 and La1.875Ba0.125CuO4, existing well above Tc and TN. The susceptibility counterpart of Cu spin polarization, derived from the muon spin relaxation rate, exhibits a divergent behavior towards T approximately 25 K. No field-induced magnetism was detected in overdoped La1.81Sr0.19CuO4, optimally doped Bi2212, and Zn-doped YBa2Cu3O7.     

Fabrication of nanofibers with uniform morphology by self-assembly of designed peptides

Fabrication of controlled peptide nanofibers with homogeneous morphology has been demonstrated. Amphiphilic beta-sheet peptides were designed as sequences of Pro-Lys-X(1)-Lys-X(2)-X(2)-Glu-X(1)-Glu-Pro. X(1) and X(2) were hydrophobic residues selected from Phe, Ile, Val, or Tyr. The peptide FI (X(1)=Phe; X(2)=Ile) self-assemble into straight fibers with 80-120 nm widths and clear edges, as examined by transmission electron microscopy (TEM) and atomic force microscopy (AFM). The fiber formation is performed in a hierarchical manner: beta-sheet peptides form a protofibril, the protofibrils assemble side-by-side to form a ribbon, and the ribbons then coil in a left-handed fashion to make up a straight fiber. These type of fibers are formed from peptides possessing hydrophobic aromatic Phe residue(s). Furthermore, a peptide with Ala residues at both N and C termini does not form fibers (100 nm scale) with clear edges; this causes random aggregation of small pieces of fibers instead. Thus, the combination of unique amphiphilic sequences and terminal Pro residues determine the fiber morphology.