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排序方式: 共有2913条查询结果,搜索用时 31 毫秒
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Abe K Ahrens LA Amako K Aronson SH Beier EW Callas JL Cutts D Diwan M Durkin LS Gibbard BG Heagy SM Hedin D Hoftun JS Hurley M Kabe S Kurihara Y Lanou RE Mann AK Marx MD Murtagh MJ Nagashima Y Newcomer FM Shinkawa T Stern E Suzuki Y Terada S White DH Williams HH Yamaguchi Y 《Physical review letters》1987,58(7):636-639
35.
Nishimiya N Yamaguchi Y Ohrui Y Suzuki M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2004,60(3):493-504
The mirror gap of a Fabry-Perot interferometer was stabilized with two laser diodes; one locked to the line frequency 385,243,555.14445 MHz of the F=3<--1 in 5D(3/2)<--5S(1/2) (87Rb) and the other to the 385,284,566.3663 MHz of the F=4<--2 in 5D(5/2)<--5S(1/2) (87Rb) [Opt. Commun. 102 (1993) 432]. The length of the mirror gap was adjusted to generate the zero-cross points simultaneously at both of the two line positions. The fringe signals obtained from an interferometer thus stabilized can be used as frequency markers having accuracies of the order of 10(10) depending on the finesse of the interferometer used. Based on measurement using Cs D1 hyperfine lines reported by Udem et al. [Phys. Rev. Lett. 82 (1999) 3568], the uncertainty of markers in the region 50 THz apart from the reference lines is +/- 5 MHz. 相似文献
36.
[structure: see text]. All stereoisomers of a cyclic alkyne containing three helicene units, 1,12-dimethylbenzo[c]phenanthrene, are synthesized using a building block. Isomeric [3 + 3]cycloalkynes aggregate in organic solvents. Vapor pressure osmometry reveals dimer formation of (M,M,M)-[3 + 3]cycloalkynes in chloroform and benzene at concentrations above 2 mM. No higher aggregation is observed. The chirality of helicenes plays an important role in self-aggregation, and diastereomeric (M,P,M)-[3 + 3]cycloalkyne forms a dimer only above 15 mM. Aggregation of racemic (M,M,M)-[3 + 3]cycloalkyne or (M,P,M)-[3 + 3]cycloalkyne is much weaker than that of a single enantiomer. 相似文献
37.
Shigeya KobayashiYoshihiro Yamaguchi Tateaki WakamiyaYoshio Matsubara Kunihisa SugimotoZen-ichi Yoshida 《Tetrahedron letters》2003,44(7):1469-1472
Simple members of arene-azaarenecyclynes as a novel family of geometrically-controlled and shape-persistent azamacrocycles have been synthesized. Noteworthy is the specific recognition function for Sb(V). The synthesized azamacrocycles, in particular the Sb(V) complex, have unusually strong light-emitting property. 相似文献
38.
Hidemasa Yamaguchi Yuji Minoura 《Journal of polymer science. Part A, Polymer chemistry》1970,8(6):1467-1479
Optically active N-bornylmaleimide (NBMI) was copolymerized with styrene, methyl methacrylate, and vinylidene chloride with a free-radical catalyst to obtain optically active copolymers. The monomer reactivity ratios for the radical copolymerization of NBMI (M2) with styrene, methyl methacrylate, and vinylidene chloride were: ST-NBMI, r1 = 0.13, r2 = 0.05; MMA-NBMI, r1 = 2.02, r2 = 0.16; VCl2-NBMI, r1 = 1.15, r2 = 0.47. The Q-e values for NBMI were Q2 = 0.48 and e2 = +1.47. The specific rotation and optical rotatory dispersion of these copolymers were measured. The correlation between the specific rotation and composition of these copolymers was not linear. The value of λc for each copolymer was independent of the copolymer composition and the comonomer, being 260 mμ for the St-NBMI system, 262 mμ for the MMA-system, and 260 mμ for the VCl2-NBMI system. The effects of solvents and temperature on the specific rotation of these copolymers were investigated. 相似文献
39.
K Sumoto M Irie N Mibu S Miyano Y Nakashima K Watanabe T Yamaguchi 《Chemical & pharmaceutical bulletin》1991,39(3):792-794
Two pyrazine derivatives [fructosazine (3) and deoxyfructosazine (6)] were simultaneously formed in a solution of D-glucosamine hydrochloride under various conditions. They showed deoxyribonucleic acid (DNA) strand breakage activity in plasmid pBR322 comparable to that of D-glucosamine. The DNA strand breakage by fructosazine (3) was stimulated by Cu2+. 相似文献
40.
S. Tamai J. Kamada T. Ono T. Kuroki K. Goto A. Yamaguchi 《Journal of polymer science. Part A, Polymer chemistry》2002,40(3):423-428
Polyimide containing an indan unit and alkyl moiety with a high molecular weight was prepared from 5,7‐diamino‐1,1,4,6‐tetramethylindan and 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride. This polyimide was amorphous and soluble in common organic solvents, such as tetrahydrofuran, chloroform, and cyclopentanone. Thermogravimetry of the polyimide showed good thermal stability, indicating that a 10% weight loss of the polyimide was observed at 500 °C in nitrogen. The glass‐transition temperature of the polyimide was not observed by DSC measurement between room temperature and 400 °C at a heating rate of 10 °C/min (Apparatus: DSC3100 MAC Science Co., Ltd.). Transparency of the polyimide at 365 nm was 80%. The polyimide acted as a photosensitive resist of negative type by UV radiation. The resist had a sensitivity of 31 mJ/cm2 and a contrast of 2.3 when it was developed with cyclopentanone at room temperature. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 423–428, 2002 相似文献