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41.
The oxygen ions of the β-VOPO4 catalyst were exchanged with an
tracer by a reduction–oxidation method and by a catalytic oxidation of but-1-ene using
2. The bands at 992 and 900 cm−1 were more shifted to lower frequencies than those at 1076 and 1002 cm−1. Applying the correlation between the Raman bands and stretching vibrations in the literature, the exchanged oxygen species were estimated. The results suggest that the P–O–V vacancies corresponding to 992 and 900 cm−1 were responsible for reoxidation and the V=O oxygen corresponding to the 1002 cm−1 band of β-VOPO4 was not. The (VO)2P2O7 was oxidized to β-VOPO4 by O2 above 823 K. The insertion position of oxygen was determined at the bands at 992 and 900 cm−1 of β-VOPO4 using
2, which is the same as the exchanged position. 相似文献
42.
Tachikawa T Tojo S Fujitsuka M Majima T 《Langmuir : the ACS journal of surfaces and colloids》2004,20(22):9441-9444
The one-electron reduction of methyl viologen (MV(2+)) mediated by the carbon dioxide radical anion (CO(2)(*-)) during photocatalytic reactions in a colloidal TiO(2) aqueous solution (pH 2) has been investigated by time-resolved absorption spectroscopy. The formation of MV(*+) generated from the one-electron reduction reaction with CO(2)(*-), which is generated from the one-electron oxidation reactions with the photogenerated holes (h(+)), was directly observed. The spectral features of the photogenerated charge carriers and the kinetic analysis of the formation process of MV(*+) revealed that the CO(2)(*-), desorbed from the surface, reacts with MV(2+) via a homogeneous electron-transfer process in the bulk solution. 相似文献
43.
In order to investigate the enzyme model reaction the oxidation of 3,4-dihydihydroxy-L-phenylalanine(L-DOPA) was carried out using optically active catalyst, N-lauroyl L or D-histidine-Cu(II) complex(L or D-LauHis-Cu(II)), showing appreciable enantioselectivity in the presence of the mixed micelles with CTABr. 相似文献
44.
Toshio Takido Sachiko Tamura Kenji Sato Haruo Kamijo Toshikatsu Nakazawa Manabu Seno Tadashi Hata 《Journal of heterocyclic chemistry》1998,35(2):437-443
The synthesis of hexahydrooxoepithiopyridinedicarboxyimide (5: X2 = N-Ph) by the reaction of thioamides 1 with N-substituted maleimide ( 2a ) was examined. The reaction of primary thioamides, such as thiobenzamide and p-toluthioamide with N-phenylmaleimide gives compounds 5 together with corresponding 4-hydroxy-1,3-thiazoles 4 . However, a similar reaction of secondary thioamides, such as N-methylthioacetamide, thiobenzanilide, with N-phenylmaleimide did not provide compounds 5 without addition of acid. The reaction pathway and the configuration of 5 were also investigated. 相似文献
45.
46.
We apply the unitarized quark model to heavy \(c\bar c\) and \(b\bar b\) quarkonium and study mass shifts and mixings induced by hadronic coupled channel effects. In particular, we study the two-meson continuum mixing in the quarkonium wave functions. It is found that the continuum component is 2–20% in the \(c\bar c\) and \(b\bar b\) states, measured as the squared sum of two-meson amplitudes \((D\bar D,D\bar D^ * + cc,D^ * \bar D^ * ,F\bar F,F\bar F^ * + cc,F^ * \bar F^ * for c\bar c)\) . It is the largest for states near or above the first threshold. These continuum mixings reduce the predicted radiative widths by 5–30%. The mass shifts of theP andF wave \(q\bar q\) states are similar to those ofS andD wave states previously studied. The computed resonance mixing matrices are explicitly given, enabling future calculations of relativistic effects, QCD effects, etc., to include also the coupled channel effects. 相似文献
47.
The electrical resistivity of the hybridized 4f-(5d/6s) system interacting with LA phonons is calculated by applying the memory function method to the periodic Anderson model in Hartree-Fock approximation. We propose a new mechanism to explain in part the anomalous resistivity of mixed valence compounds such as CePd3. For finite hybridizationV a finite fraction of 4f electrons participates in electrical conduction leading to an essential change of the normald band current. Resistivity and the fraction of 4f electrons increase with increasing value of [V/(E–)]2 where (E–) is the distance between the effective positionE of the 4f level and the chemical potential. In typical mixed valence systems [V/(E–)]2 is strongly temperature dependent and decreases with increasing temperature. This explains the high temperature resistivity behaviour of CePd3. For (E–) being small compared to the Debye-temperature the resistivity is enhanced and becomes extremely sensitive to small changes of (E–).Work performed within the research program of the Sonderforschungsbereich 125, Aachen-Jülich-Köln 相似文献
48.
N Otsuka M Fukunaga K Morita S Ono K Nagai T Furukawa S Yanagimoto T Tomomitsu H Kawahara H Tanaka 《Radioisotopes》1988,37(6):330-335
In order to detect the varicocele, scrotal scintigraphies by using 99mTc-HSA-D were performed in 14 patients with male infertile or palpable mass in left scrotum on physical examinations. Abnormal pooling of 99mTc-HSA-D, indicative of varicocele lesion, could be found in left scrotum in 9 cases, confirmed surgically or clinically. Compared with 99mTc-HSA, 99mTc-HSA-D was superior in high uptake ratio of varicocele to soft tissue and in nonvisualization of bladder. Thus, 99mTc-HSA-D scrotal scintigraphy seemed to be of a great use to detect the varicocele. 相似文献
49.
Enzymatic transformations into cyclic oligomers were carried out with the objective of developing chemical recycling of poly(lactic acid)s, such as poly(D,L-lactic acid) (PDLLA), poly(D-lactic acid) (PDLA) and poly(L-lactic acid) (PLLA), which are typical biodegradable polymers. They were degraded by lipase in an organic solvent to produce the corresponding cyclic oligomer with a molecular weight of several hundreds. PDLLA (with a Mw of 84,000) was quantitatively transformed into cyclic oligomers by lipase RM (Lipozyme RM IM) in chloroform/hexane at 60 degrees C. PLLA (with a Mw of 120,000) was transformed into cyclic oligomer by lipase CA (Novozym 435) at a higher temperature of 100 degrees C in o-xylene. The oligomer structure was identified by 1H and 13C NMR spectroscopy and MALDI-TOF (matrix assisted laser desorption/ionization-time-of-flight) mass spectrometry. 相似文献
50.
Yasuhiro Ono Ryuji IshikawaYuzuru Miyazaki Yoshinobu IshiiYukio Morii Tsuyoshi Kajitani 《Journal of solid state chemistry》2002,166(1):177-181
The layered oxide thermoelectric material β-Na0.67CoO2 has been studied by powder neutron diffraction, electric and magnetic measurements. This compound includes an edge-sharing CoO6 slab and a highly vacant Na+ sheet in a unit cell (space group symmetry C2/m, a=4.9023(4) Å, b=2.8280(2) Å, c=5.7198(6) Å and β=105.964(6)° at 300 K). The evaluated formal valence of cobalt ion, +3.33(1), is ascribed to the coexistence of Co3+ and Co4+ in the ratio 2:1. Polycrystalline β-Na0.67CoO2, a p-type thermoelectric material, exhibits metallic behavior of the electric resistivity below 300 K. The Curie-Weiss-type magnetic susceptibility indicates antiferromagnetic interactions between magnetic cobalt ions in the edge-sharing CoO6 slab. 相似文献