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51.
[chemical reaction: see text]. Two novel insecticidal antibiotics with a p-methoxyphenylquinolinone skeleton fused with a pyran ring, yaequinolones J1 (1) and J2 (2), have been isolated from Penicillium sp. FKI-2140, and structures were elucidated by spectroscopic studies including various NMR experiments. The relative stereochemistries were assigned by NOE experiments. Yaequinolones J1 and J2 showed toxicity against Artemia salina (brine shrimp) with the MIC value of 6.25 microg/mL. 相似文献
52.
Noriko Hata Shiho Hieda Mika Yamada Rie Yasui Hideki Kuramitz Shigeru Taguchi 《Analytical sciences》2008,24(7):925-928
The formation of a liquid organic ion associate in an aqueous sample was applied to the concentration and determination of cadmium in environmental water samples. Cadmium was converted into a complex with 2-(5-bromo-2-pyridylazo)-5-(N-propyl-N-sulfopropylamino)phenol (5-Br-PAPS) in a 40-mL sample solution, and was extracted into a liquid ion associate of phenolsulfonate and benzethonium during phase formation. More than 400-fold enrichment was easily attained by this technique, because the volume of the liquid organic phase formed was very small, ca. 2 microL. After dilution of the organic phase with a small volume of 2-methoxyethanol, the cadmium in the solution was determined by GF-AAS. The detection limit was 0.09 ng/L (3sigma(b)). This method was applied to the determination of cadmium in river water and seawater. 相似文献
53.
Anatolij Dvurečenskij Beloslav Riečan 《International Journal of Theoretical Physics》1994,33(7):1387-1402
We present a general decomposition theorem for elements of an ordered group with respect to a cone. This result enables us to obtain decompositions of finitely additive measures defined on quantum logics, orthoalgebras, or, more generally, on difference posets with values in Dedekind complete lattice ordered groups, with respect to a given cone of measures. In particular, we gain Yosida-Hewitt-type and Lebesgue-type decompositions. 相似文献
54.
This study proposes a novel approach to construct the orbital-specific (OS) hybrid exchange-correlation functional by imposing the linearity condition: ?(2)E/?f(i)(2)|(0≤f(i)≤1) = ??(i)/?f(i)|(0≤f(i)≤1) = 0, where E, ε(i), and f(i) represent the total energy, orbital energy, and occupation number of the ith orbital. The OS hybrid exchange-correlation functional, of which the OS Hartree-Fock exchange (HFx) portion is determined by the linearity condition, reasonably reproduces the ionization potentials not only from valence orbitals but also from core ones in a sense of Koopmans' theorem. The obtained short-range HFx portions are consistent with the parameters empirically determined in core-valence-Rydberg-Becke-3-parameter-Lee-Yang-Parr hybrid functional [Nakata et al., J. Chem. Phys., 124, 094105 (2006); ibid, 125, 064109 (2006)]. 相似文献
55.
The reactions of (μ-NPh2)2Al2Me4 and of μ-NPh2 -μ-MeAl2Me4 with trimethylamine, diethyl ether and dimethyl sulfide have been investigated. These studies establish that the bases cleave the nitrogen bridged system (μ-NPh2)2 Al2Me4 to give adducts of formula Me2Al(NPh2) · B. The relative stabilities of the adducts formed appear to be in the order NMe > OEt2 >SMe2, with thesulfide adduct apparently dissociated even at ?74°. μ-NPh2-μ-MeAl2Me4 reacts with a limited supply of base to give Me3Al · B and (μ-NPh2)2 Al2 Me4, and additional base cleaves (μ-NPh2)2Al2Me4 as before. 相似文献
56.
Rie Takagi Fabienne Duc Mats Johnsson 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(2):i16-i18
Single crystals of molybdenum(VI) tricopper(II) tellurium(IV) heptaoxide dichloride hemihydrate, MoCu3TeO7Cl2·0.5H2O, were synthesized via a transport reaction in sealed evacuated silica tubes. All atoms occupy general positions within the triclinic () unit cell. The building units are irregular CuO4Cl and CuO3Cl2 square pyramids, distorted TeO3+1E trigonal bipyramids (E is the lone pair of TeIV) and irregular MoO5 pyramids. The TeO3+1E, CuO4Cl and CuO3Cl2 polyhedra form (110) layers bridged by Mo atoms. The water molecules are located in [100] channels. 相似文献
57.
Investigations of the discharge for PA-CVD of TiN on steel substrates are carried out using optical emission spectroscopy. A great number of species could be identified in the discharge. The growth rate of dense layers shows a direct dependence on Ti+ intensities. The occurrence of TiN in the discharge leads to f aky, not compact layers, lowering the hardness of the layers. 相似文献
58.
Jan Paseka Sylvia Pulmannová Zdenka Riečanová 《International Journal of Theoretical Physics》2013,52(6):1994-2000
We study a generalized effect algebra of unbounded linear operators in an infinite-dimensional complex Hilbert space. This algebra equipped with a certain kind of topology allows us to show that unbounded quasi-Hermitian operators can be expressed as a difference of two infinite sums of bounded quasi-Hermitian operators. 相似文献
59.
Osamu Sato Shinya Hayami Zhong-ze Gu Kazuyuki Takahashi Rie Nakajima Akira Fujishima 《Phase Transitions》2013,86(7-8):779-785
Photo-illumination effects have been measured for the compound [Co III-LS (tmpda)(3,6-DBSQ)(3,6-DBCat)]. When the aforementioned compound was illuminated at 5 K, the magnetization value increased from w eff = 1.87 to 2.03 w B . The absorption spectra after illumination show that the absorption band at around 730 nm, which is characteristic of the [Co II-HS (tmpda)(3,6-DBSQ) 2 ] state, increased in intensity and that the charge transfer band from 3,6-DBCat to 3,6-DBSQ at 2500 nm was reduced in intensity. IR spectra show that the C-O stretching peak at 1279 cm m 1 is decreased in intensity. These results confirm that a photo-induced intra-molecular electron transfer, [Co III-LS (tmpda)(3,6-DBSQ)(3,6-DBCat)] to; [Co II-HS (tmpda)(3,6-DBSQ) 2 ], was induced. The lifetime of the metastable state at 5 K was 15 min. Furthermore, it was found that reverse valence tautomerism can be induced by exciting the Co II-HS to 3,6-DBSQ charge transfer band in metastable [Co II-HS (tmpda)(3,6-DBSQ) 2 ]. 相似文献
60.
Takashi Fujikawa Hiroko Arai Rie Suzuki Hiroshi Shinotsuka Lszl Kvr Nobuo Ueno 《Journal of Electron Spectroscopy and Related Phenomena》2008,162(3):146-157
Recoil effects of photoelectrons excited by high-energy X-rays are studied beyond the simplest approximation where elastic scatterings of photoelectrons are completely neglected (single-site approximation). At first we have shown that the simple free atom energy shift is accurately obtained within the harmonic and the single-site approximations. Beyond the single-site approximation, this simple formula does not work, but still simple classically acceptable formula can be used to explain the recoil energy shift. Illustrative numerical calculations show that the energy shifts caused by the photoelectron diffraction amounts to 5–8 meV for graphite-like carbon and about 100 meV for LiI6 cluster at ?k=5–7 keV, and show oscillations as functions of the photoelectron energy. Furthermore we discuss the recoil effects in photoemission from extended levels by use of the tight-binding approach. Our approach naturally provides not only Debye–Waller factors but also the recoil factors. In addition to the phonon excitation, we also study the recoil effects associated with plasmon losses where intrinsic and extrinsic processes can interfere each other. Only the latter can contribute to the recoil energy shift. 相似文献