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81.
Mariame A. Hassan Loreto B. Feril Kosho Suzuki Nobuki Kudo Katsuro Tachibana Takashi Kondo 《Ultrasonics sonochemistry》2009,16(3):372-378
Three novel lipid-shell-type microbubbles (MBs), AS-0100, BG6356A and BG6356B, have been evaluated for their impact on ultrasound (US)-induced cell death and free radicals production. Previously studied and well-characterized US exposure conditions were employed in which human myelomonocytic lymphoma U937 cells were exposed to 1 MHz pulsed US beam (0.3 W/cm2, 10% duty factor) for 1 min with or without MBs. Three different concentrations of each MB were used. Apoptosis and cell lysis were assessed by examining phosphatidylserine externalization and by counting viable cells, respectively, 6 h post-exposure. Free radicals production and scavenging activities were evaluated using electron paramagnetic resonance (EPR)-spin trapping. The results showed that only AS-0100 and BG6356A were able to enhance the US-induced apoptosis, mainly by increasing the secondary necrosis. Apoptosis and cell lysis seemed to depend more on mechanical forces exerted by oscillating MBs while free radicals played a trivial role. BG series MBs exhibited pronounced scavenging activities. Generally, despite the need for further optimization, AS-0100 and BG6356A appear to be promising as adjuncts in cases where US-induced cell death is required. 相似文献
82.
Hideo Kaiju Akito Ono Kenji Kondo Jonghan Won Manabu Ishimaru 《Applied Surface Science》2009,255(6):3706-3712
We study the structural properties of the surface roughness, the surface mound size and the interfacial structure in Ni thin films vacuum-deposited on polyethylene naphthalate (PEN) organic substrates with and without the application of magnetic field and discuss its feasibility of fabricating quantum cross (QC) devices. For Ni/PEN evaporated without the magnetic field, the surface roughness decreases from 1.3 nm to 0.69 nm and the surface mound size increases from 32 nm to 80 nm with the thickness increased to 41 nm. In contrast, for Ni/PEN evaporated in the magnetic field of 360 Oe, the surface roughness tends to slightly decrease from 1.3 nm to 1.1 nm and the surface mound size shows the almost constant value of 28-30 nm with the thickness increased to 35 nm. It can be also confirmed for each sample that there is no diffusion of Ni into the PEN layer, resulting in clear Ni/PEN interface and smooth Ni surface. Therefore, these experimental results indicate that Ni/PEN films can be expected as metal/insulator hybrid materials in QC devices, leading to novel high-density memory devices. 相似文献
83.
84.
Michiro Kondo 《Mathematica Slovaca》2014,64(5):1093-1104
We define states on bounded commutative residuated lattices and consider their property. We show that, for a bounded commutative residuated lattice X,
- If s is a state, then X/ker(s) is an MV-algebra.
- If s is a state-morphism, then X/ker(s) is a linearly ordered locally finite MV-algebra.
- s is a state-morphism on X.
- ker(s) is a maximal filter of X.
- s is extremal on X.
85.
Dr. Masaki Yoshida Dr. Mio Kondo Prof. Toshikazu Nakamura Prof. Ken Sakai Prof. Shigeyuki Masaoka 《Angewandte Chemie (International ed. in English)》2014,53(43):11519-11523
A series of [{(terpy)(bpy)Ru}(μ‐O){Ru(bpy)(terpy)}]n+ ( [RuORu]n+ , terpy=2,2′;6′,2′′‐terpyridine, bpy=2,2′‐bipyridine) was systematically synthesized and characterized in three distinct redox states (n=3, 4, and 5 for RuII,III2 , RuIII,III2 , and RuIII,IV2 , respectively). The crystal structures of [RuORu]n+ (n=3, 4, 5) in all three redox states were successfully determined. X‐ray crystallography showed that the Ru? O distances and the Ru‐O‐Ru angles are mainly regulated by the oxidation states of the ruthenium centers. X‐ray crystallography and ESR spectra clearly revealed the detailed electronic structures of two mixed‐valence complexes, [RuIIIORuIV]5+ and [RuIIORuIII]3+ , in which each unpaired electron is completely delocalized across the oxo‐bridged dinuclear core. These findings allow us to understand the systematic changes in structure and electronic state that accompany the changes in the redox state. 相似文献
86.
The structures of two new dimeric acridone alkaloids, glycobismine-D (1) and -E (2), having a novel linkage as binary acridones, three monomeric acridones, glycocitrine-IV (3), -V (4), and -VI (5), and three quinolone alkaloids, glycocitlone-A (6), -B (7), and -C (8) from Glycosmis citrifolia (Willd.) Lindl. (Rutaceae) have been elucidated by spectrometric studies. 相似文献
87.
Naofumi Akata H. Kawabata H. Hasegawa T. Sato Y. Chikuchi K. Kondo S. Hisamatsu J. Inaba 《Journal of Radioanalytical and Nuclear Chemistry》2008,277(2):347-355
The atmospheric concentrations and deposition fluxes of 7Be and 210Pb were observed biweekly in Rokkasho, Japan on the Pacific Ocean coast at the northern end of Honshu Island, from March 2000
to March 2006, to clarify their regional features. Seasonal variation pattern of atmospheric 7Be concentrations had double peaks, and that of 210Pb had a single peak. Deposition fluxes of 7Be and 210Pb showed the same patterns. The total deposition pattern of 7Be was similar to that commonly seen on the Pacific Ocean side of northern Honshu Island, while the pattern of 210Pb was similar to that commonly seen on the Japan Sea side. The lack of high spine mountains windward in Rokkasho may be the
cause of this ambiguity in the winter monsoon season. Total deposition velocities and scavenging ratios of 210Pb were similar to those of 7Be from spring to fall, and showed that both nuclides had a similar removal process from the atmosphere. However, the scavenging
ratios of 210Pb were slightly larger than those of 7Be in winter, indicating different behaviors for both nuclides in the scavenging process. The scavenging ratios of both nuclides
inversely correlated with precipitation rate, and the ratios in winter were larger than in the other seasons. 相似文献
88.
Nagata M Kondo M Suemori Y Ochiai T Dewa T Ohtsuka T Nango M 《Colloids and surfaces. B, Biointerfaces》2008,64(1):16-21
Dialkyl disulfide-linked naphthoquinone, (NQ-Cn-S)2, and anthraquinone, (AQ-Cn-S)2, derivatives with different spacer alkyl chains (Cn: n = 2, 6, 12) were synthesized and these quinone derivatives were self-assembled on a gold electrode. The formation of self-assembled monolayers (SAMs) of these derivatives on a gold electrode was confirmed by infrared reflection-absorption spectroscopy (IR-RAS). Electron transfer between the derivatives and the gold electrode was studied by cyclic voltammetry. On the cyclic voltammogram a reversible redox reaction between quinone (Q) and hydroquinone (QH2) was clearly observed under an aqueous condition. The formal potentials for NQ and AQ derivatives were −0.48 and −0.58 V, respectively, that did not depend on the spacer length. The oxidation and reduction peak currents were strongly dependent on the spacer alkyl chain length. The redox behavior of quinone derivatives depended on the pH condition of the buffer solution. The pH dependence was in agreement with a theoretical value of E1/2 (mV) = E′ − 59pH for 2H+/2e− process in the pH range 3–11. In the range higher than pH 11, the value was estimated with E1/2 (mV) = E′ − 30pH , which may correspond to H+/2e− process. The tunneling barrier coefficients (β) for NQ and AQ SAMs were determined to be 0.12 and 0.73 per methylene group (CH2), respectively. Comparison of the structures and the alkyl chain length of quinones derivatives on these electron transfers on the electrode is made. 相似文献
89.
T. Kobayashi I. Endo A. Fukumi T. Horiguchi Y. Ishida T. Kondo T. Kuwamoto N. Minamoto T. Nakamura T. Takahasi 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1997,39(3):209-216
Atomic-beam laser spectroscopy with fluorescence detection is applied to investigate the hyperfine structure (hfs), Stark and Zeeman effects of the electric dipole transitions of Sm i. The measurements are performed for the four transitions of 0 → 15650.55, 292.58 → 15650.55, 292.58 → 15567.32, and 1489.55 → 16890.59 cm-1. The hfs constants of the upper and lower levels and the isotope shifts of the transitions are determined. The tensor polarizability of the 15650.55 cm-1 level is found to be α2 = -556.2 ± 11.8 kHz/(kV/cm)2. Thanks to the accurate g values of the lower levels [Childs, W.J., Goodman, L.S.: Phys. Rev. A 6, 2011 (1972)], the g values of the upper levels are obtained from the observed Zeeman splittings. The values are found to be -0.115907(79), 2.22259(20) and 1.599968(51) for the 15650.55 cm-1 .1, 15567.32 cm-1 and 16890.59.cm-1 levels, respectively. 相似文献
90.
A novel oxidative cyclization of quinone-arenols 5 leading to products 6 with a dibenzofuran-1,4-dione structure, which forms the core of several natural products, has been developed and applied to the synthesis of violet-quinone (4). 相似文献