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261.
Kazuo Sasazawa Yuko Yamada Akiko Fujisawa Toshikazu Saitoh Katsuya Ueno Kazuya Oharu Hideo Sawada 《Colloid and polymer science》2005,283(7):812-816
Self-assembled fluorinated molecular aggregates formed by fluoroalkyl end-capped N-(1,1-dimethyl-3-oxobutyl)acrylamide oligomers, N,N-dimethylacrylamide oligomers, and acrylic acid oligomers in methanol could selectively recognize fluoresceins as guest molecules to form a new class of fluorinated aggregates-fluorescein nanocomposites. These fluorinated fluorescein nanocomposites that are obtained exhibit an extraordinarily enhanced light absorption (max ca. 440 nm) compared to that (maxs 452, 480 nm) of the parent fluorescein in the absence of fluorinated aggregates. 相似文献
262.
Photochemical efficiency of o-quinodimethane (3) ring closure at room temperature was determined by using a time-delayed, two-color photolysis technique. o-Quinodimethane (3) was generated by the photolysis of 1,2-bis[(phenylseleno)methyl]benzene (1) by a KrF (248 nm) laser pulse and thus-generated 3 was photolyzed by a subsequent XeCl (308 nm)/XeF (351 nm) laser pulse with varying delay time of 0 to 3 s. The time profile of 3 was monitored by the chemical analyses of benzocyclobutene (5) (a photochemical product of 3), which was formed by a one-photon process, and the spiro dimer of 3 (4) (a thermal product of 3) in the two-color photolysis experiments. The time profile of 3 followed a second-order decay kinetics. The photochemical efficiency was obtained by the analysis of the delay-time dependence of the product yields; those of the consumption of 3 and the conversion 3-->5 by a single pulse of the excimer laser were 81% and 5.7% for the XeCl laser, and 73% and 2.3% for the XeF laser. This difference was attributed to the different excited states involved in the photolysis. In contrast to the photolysis of 3 in argon or rigid organic matrixes, it was revealed that photochemical conversion 3-->5 was not the main path in the solutions, and intermolecular reactions predominated. 相似文献
263.
Yuko Yamaura Takao Odake Akifumi Suzuki Mamiko Fujii Kiyoshi Nakayama 《Optical Review》2003,10(5):411-414
To understand the optical properties of living tissue in the NIR range, it appeared informative to investigate the scattering properties of high concentration particle suspension. We measured the angular light scattering of aqueous suspension of 3.5 μmφ polystyrene particles contained in a 60 μm thick cuvette up to 50% volume concentration at 805 nm wavelength using a goniophotometer. We found that the discrepancy between the measurement and the Monte Carlo simulation becomes larger with increased concentration, which is attributable to the phase function change as well as the scattering coefficient change. 相似文献
264.
Tatsuro Ouchi Satoshi Jokei Hidenori Chikashita 《Journal of heterocyclic chemistry》1982,19(4):935-936
1,2:5,6-Di-O-isopropylidene-3-O-[3-(uracil-1-yl)propionoyl]-α-D-glucofuranose and 1,2-mono-O-isopropylidene-6-O-[3-(uracil-1-yl)propionoyl]-α-D-glucofuranose were synthesized. 相似文献
265.
Tatsuro Ouchi Tomohiro Kontani Yuichi Ohya 《Journal of polymer science. Part A, Polymer chemistry》2003,41(16):2462-2468
Polylactide (PLA)‐grafted dextran was synthesized with a trimethylsilyl protection method to produce novel biodegradable, biomedical materials. PLA‐grafted dextrans with various lengths and numbers of graft chains were synthesized. The properties of solution‐cast films prepared from PLA‐grafted dextrans were investigated with thermal and dynamic mechanical analyses. The graft‐copolymer films exhibited lower glass‐transition temperatures, melting temperatures (Tm's), and crystallinities as well as higher viscosity properties as compared with poly‐L ‐lactide film. The Tm and crystallinity and mechanical properties at 37 °C could be adjusted by controlling the molecular structure such as the lengths and numbers of graft chains. Furthermore, the biodegradability of PLA‐grafted dextran films was investigated through the weight change of film and the molecular weight change of polymer during the in vitro degradation test. PLA‐grafted dextrans exhibited different degradation behavior from poly‐L ‐lactide with the introduction of a polysaccharide segment and branched structure as well as the change of end‐functional group. The degradation rate of PLA‐grafted dextran and the cast film prepared from PLA‐grafted dextran could be adjusted by controlling the sugar content or the length of graft chains. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2462–2468, 2003 相似文献
266.
267.
Yukio Kubota Yuko Motosa Yoko Shigemune Yasuo Fujisaki 《Photochemistry and photobiology》1979,29(6):1099-1106
Abstract— All nucleotides examined (AMP, GMP, TMP and CMP) quench the fluorescence or 10–methylacridinium chloride (10–MEAC). The fluorescence spectrum of 10–MEAC-nucleotide system is identical with that of 10–MEAC itself, and the fluorescence decay kinetics follow a single-exponential decay law. The dependence of fluorescence quantum yields and fluorescence lifetimes upon the concentration of nucleotides indicates that the fluorescence of 10–MEAC is greatly quenched in both dynamic and static processes by nucleotides. The quenching constants increase in the order: AMP ≳ GMP > TMP ≳ CMP. The results of 10–MEAC are compared with those of other acridine dyes (proflavine, 9–aminoacridine and acridine orange). 相似文献
268.
K. Ouchi 《Optics Communications》1978,24(3):273-275
The contrast of a speckle pattern formed by a conventional imaging system has been experimentally investigated. A dip in contrast of the speckle pattern produced near the focal plane and the image plane has been observed. It is also found that the variation of contrast along the optical axis of the imaging system with a hard-edged aperture differs considerably from that with a soft aperture. 相似文献
269.
270.
Fujimori A Nakahara H Ito E Hara M Kanai K Ouchi Y Seki K 《Journal of colloid and interface science》2004,278(1):184-191
With comb polymers with different kinds of fluorocarbon side-chains, significant effects of spreading solvents on the monolayers at the air/water interface and the molecular arrangement in the deposited films could be found by the use of trifluoroacetic acid and its mixed solvents with n-hexane, depending on the atoms, fluorine or hydrogen, substituted at the end of the fluorocarbon side-chains. These facts are probably due to intralayer hydrogen bonding cooperating with the carbonyl groups of the long-chain esters. The deposited films of solid substrates were characterized by polarized near-edge X-ray absorption fine structure (NEXAFS) spectroscopy as well as in-plane X-ray diffraction and scanning electron and atomic force microscopy. 相似文献