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111.
Yasuo Kimura Takashi Hamasaki Hiromitsu Nakajima Akira Isogai 《Tetrahedron letters》1982,23(2):225-228
Aszonalenin () has been isolated from together with LL-S490β () and the structure of has been established by spectroscopic evidences and chemical transformation. 相似文献
112.
We revisited the vanadium oxide phosphors, AVO3 (A:K, Rb, and Cs) and M3V2O8 (A:Mg and Zn) for a revaluation of possibility of these compounds for lighting applications, and the internal quantum efficiency (η) and luminescent colour properties for AVO3 (A:K, Rb, and Cs) and M3V2O8 (A:Mg, and Zn) have been presented. The AVO3 showed the broadband emission from 380 to 800 nm, and the η for the KVO3, RbVO3 and CsVO3 were 4%, 79% and 87%, respectively. The CIE colour coordinates are located at white region on the chromaticity diagram. The M3V2O8 (A:Mg and Zn) also exhibited a quite broadband emission between 410 and 900 nm, indicating yellow luminescent colour. The Zn3V2O8 showed high η value, 52%, compared to that of the Mg3V2O8 (η=6%). This enhancement of η in the Zn3V2O8 could be due to the increasing exciton diffusion assisted by the hybridizations of Zn 3d and O 2p orbitals for the valence band, and Zn 4s and Ti 3d orbitals for the conduction band. 相似文献
113.
We examined the formation of complexes between terbium ion (Tb3+) and carbohydrates labeled with aminobenzene compounds. Of the examined compounds, carbohydrates labeled with 4-aminosalicylic acid showed intense fluorescence with Tb3+ in the presence of cetylpyridinium chloride at pH 6.0. Calibration curves for maltose derivative showed good linearity between 5 pmol and at least 600 pmol, with good reproducibility. We applied the proposed technique to binding studies between manno-oligosaccharides and Concanavalin A. 相似文献
114.
Formation of cyclic compounds from zirconacycles has been performed by a combination of Michael addition and coupling with an alkenyl iodide moiety in the presence of a stoichiometric amount of CuCl. The reaction of 3-iodopropenoates with various zirconacyclopentadienes in the presence of a stoichiometric amount of CuCl afforded penta- and hexasubstituted cyclopentadienes. The reaction of 3-iodocycloenones with zirconacyclopentadienes, zirconacyclopentenes, or zirconacyclopentanes gave spirocyclic compounds in good yields. 相似文献
115.
Ohne Zusammenfassung 相似文献
116.
117.
Toshie Tahara Yoshitsugu Sakuda Mitsuaki Kodama Yoshimasa Fukazawa Shô Itô Kazuyoshi Kawazu Shuhei Nakajima 《Tetrahedron letters》1980,21(19):1861-1862
The structures of xantholides A and B were deduced on the basis of IR and NMR spectra, and confirmed by X-ray analysis. Xantholide A inhibited the larval growth of Drosophila melanogaster. 相似文献
118.
119.
Shinohara Y Kawasaki N Ueno S Kobayashi I Nakajima M Amemiya Y 《Physical review letters》2005,94(9):097801
Crystallization of n-hexadecane in emulsion droplets was studied using time-resolved two-dimensional small- and wide-angle x-ray scattering with differential scanning calorimetry (2D-SAXS-WAXS-in situ DSC) which provides information about both nano- and subnanoscale structural change. n-hexadecane in droplets reproducibly crystallized into the stable triclinic phase via a transient-rotator phase. This is in contrast with previous results that the rotator phase of n-hexadecane was observed only occasionally for bulk samples. Thus we confirmed the existence of rotator phase in n-hexadecane, which is important for the study of crystallization of soft materials. We suggest that the rotator phase at the interface of oil and water plays a precursor role for bulk crystallization. This study demonstrates that 2D-SAXS-WAXS-in situ DSC is a powerful tool for the study of a transient phase. 相似文献
120.
Anion photoelectron spectroscopy of acetonitrile cluster anions, (CH3CN)(-)(n) (n=10-100), successfully demonstrates the competitive coexistence of two different anionic species: a solvated electron and a solvent-bound valence anion. The distinctly different nature of these anions is revealed by hole-burning-type photoelectron spectroscopy and relative photodetachment cross section measurements. This unusual coexistence is attributed to the closely lying nature of their anionic states at just the number of solvent molecules sufficient to almost complete the first solvation layer. 相似文献