Photoinduced nitric oxide release from nitrobenzene derivatives

A new type of photoinduced nitric oxide (NO) donors was designed from nitrobenzene derivatives. Visible-light irradiation of 2,6-dimethylnitrobenzenes bearing extended pi-electron systems at the 4-position revealed efficient NO release using ESR analysis and the Griess assay. Computational study and ultraviolet spectrum analysis suggested that the NO-releasing activity was closely related to the conformation of the nitro group, the absorption intensity, and the length of the conjugated pi-electron system. Employing the photodependent cytotoxicity of compound 14 against HCT116 human colon cancer cells, it was demonstrated that 4-substituted-2,6-dimethylnitrobenzene analogues are useful NO donors for the time- and site-controlled NO treatment.     

Water-soluble constituents of caraway: carvone derivatives and their glucosides

Nine monoterpenoids related to carvone and seven glucosides were isolated from the water-soluble portion of the methanolic extract of the caraway (fruit of Carum carvi L.), and their structures were clarified by spectral investigation. Among them, eight monoterpenoids and six glucosides were new.     

Synthesis and absolute configuration of a new 3,4-dihydro-beta-carboline-type alkaloid, 3,4-dehydro-5(S)-5-carboxystrictosidine,isolated from Peruvian Uña de Gato (Uncaria tomentosa)

The structure including the absolute configuration of a new glucoalkaloid, 3,4-dehydro-5(S)-5-carboxystrictosidine, isolated from Peruvian U?a de Gato (Cat's Claw, original plant: Uncaria tomentosa), was confirmed by synthesis starting from secologanin and L-tryptophan.     

Isolation and structure elucidation of two new alkaloids,pandamarilactonine-C and -D,from Pandanus amaryllifolius and revision of relative stereochemistry of pandamarilactonine-A and -B by total synthesis

Two new pyrrolidine alkaloids, pandamarilactonine-C and -D, were isolated from Pandanus amaryllifolius. Based on the total synthesis of pandamarilactonine-C and its related alkaloid, pandamarilactonine-A, the relative stereochemistry of pandamarilactonine-A and -B, which was previously proposed by spectroscopic analysis, was revised.     

Dynamics of coherent anharmonic phonons in bismuth using high density photoexcitation

We have investigated the dynamical properties of the coherent anharmonic phonons generated in Bi under high density excitation. The time-resolved reflectivity in the intensely photoexcited Bi film is modulated by the coherent A(1g) phonon oscillation with a time-dependent oscillation period. As the pump power density is increased, the line shape of the A(1g) mode in the Fourier transformed spectra becomes asymmetric, and the redshift of the phonon frequency is observed. Analysis of the transient redshift with a wavelet transform reveals that the frequency of the A(1g) mode depends on the squared amplitude of the oscillation, which is attributed to an anharmonicity of the lattice potential.     

An ESR-CT imaging of the head of a living rat receiving an administration of a nitroxide radical.

Three-dimensional ESR imaging of a living rat has been performed by an L-band ESR system, which is composed of an L-band ESR spectrometer, a field gradient coil, and a data processor. The imaging was carried out by Lauterbur's method. A nitroxide, 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl (Carbamoyl-PROXYL), was used as an imaging agent in saline solution at a concentration of 0.2 M and administered intraperitoneally to obtain a constant concentration in the head for about an hour. It took about 40 min to obtain one set of ESR-CT images. The cross-sectional images were made, both as coronal and horizontal images. In the images of the rat head the nitroxide-rich region was clearly distinguished from the deficient region. The nitroxide-deficient areas corresponded well to the brain of the rat.     

In situ spectroscopic measurement of structural change in SiO2 during femtosecond laser irradiation

Spectra of light transmitted through SiO₂ specimens were measured during irradiation of amplified 800 nm ultrashort (400 fs) laser with a repetition rate of 100 kHz. The spectra exhibit a broad dispersion including a peak at around 450 nm, and the peak wavelength and the intensity are found to significantly depend on the irradiation time. Positively charged oxygen vacancies (E center) and oxygen-deficiency centers (ODCs) with neutral charge were observed by electron spin resonance (ESR) and photoluminescence (PL), respectively, after irradiation. The formation of the E center and the subsequent transformation to ODCs significantly depend on the laser power density. The correlation between the intensity of the peak at around 450 nm and the ESR signal intensity of the E center, and also the observation of PL spectrum due to ODCs suggest that self-trapped excitons exhibiting the peak at around 450 nm are created through multi-photon absorption, followed by the formation of the E center, and this finally leads to the formation of ODCs. PACS 78.47.+p; 61.80.Ba; 76.30.Mi     

On the nature of coherent phonons generated by ultrashort laser pulses in single-crystal antimony

Reflectivity oscillations generated by A_1g coherent phonons in an antimony single crystal have been studied by a method involving pumping and probing by femtosecond laser pulses, which was complemented by spectral filtration of the signal. An analysis of the spectrally resolved signal showed that not only the integrated intensity but also the spectrum of the probe pulse are functions of the delay time between the pumping and probing and oscillate between the Stokes and anti-Stokes components at the optical-phonon frequency. A comparison of the integrated lattice excitation relaxation dynamics with the spectrally resolved lattice excitation relaxation dynamics revealed new facets in the nature and generation mechanism of coherent phonons.     

Glycosides of Atractylodes ovata

A new coumarin glycoside and a new glycoside of an acetylene derivative were isolated from the water-soluble portion of the methanolic extract of Atractylodes ovata rhizome together with eight known compounds. Their structures were characterized as scopoletin beta-D-xylopyranosyl-(1-->6)-beta-D-glucopyranoside and (2E)-2-decene-4,6-diyne-1,8-diol 8-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside, respectively, based on chemical and spectroscopic investigations. A comparison of the polar constituents among Atractylodes japonica, Atractylodes lancea, and A. ovata is led to the conclusion that A. ovata is distinguishable from A. lancea and A. japonica, as also shown by phylogenetic analysis.     

Polymorphic forms of nylon 3

The crystal structure of nylon 3 was studied, and four crystalline modifications were observed. Modification I, as determined from the x-ray diffraction pattern of drawn fibers, is similar to the α crystal structure of nylon 6. The unit cell is monoclinic; a = 9.33 Å, b = 4.78 Å, (fiber identity period), c = 8.73 Å, and β = 60°. The theoretical density for nylon 3 with four monomeric units in the unit cell is 1.39 g/cm³, and the observed density is 1.33 g/cm³. The space group is P2₁. The nylon 3 chains are in the extended planar zigzag conformation. Although other odd-numbered nylon form triclinic or pseudohexagonal crystals when oriented, drawn nylon 3 crystals are monoclinic. In addition to modification I, modifications II, III, and IV were studied. Lattice spacings of modifications II and III are equal to those of modification I. However x-ray diffraction intensities are different. Infrared spectra of those forms indicate an extended planar zigzag conformation of the chains. Modification IV is thought to correspond to the so-called smectic hexagonal form. No γ crystals were found, and it appears that polyamide chains with short sequences of methylene groups cannot form crystals of this type.