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A.M. El-Badry T. Kuroyanagi S. Mitarai A. Odahara Y. Gono S. Morinobu K. Ogawa 《The European Physical Journal A - Hadrons and Nuclei》1998,3(2):133-138
A recoil distance method was used to measure half-lives of the excited states of 145Sm. The reaction used was 139La(10B, 4n)145Sm. A plunger system was used. Half-lives were determined for two excited states for the first time. The yrast 27/2+ state was found to have a half-life of 1.1 ± 0.2 ns corresponding to the retardation of 3.1 × 10−4 comparing with the single particle estimate of M1. The excitation energy of this state was well reproduced by the shell model
calculation having a mixed configuration of [π{h11/2(g7/2)−2 (d5/2)−1}10−, νf7/2] + [π{h11/2(g7/2)−1}9−,νh9/2]. Another retarded E1 transition was also found in a decay of a 21/2+ state. Its retardation was 1.6 × 10−4 comparing with the single particle value.
Received: 9 September 1997 / Revised version: 12 June 1998 相似文献
23.
Kim GN Kim EJ Son D Bacala A Imlay R Kirk P McNeil RR Metcalf W Cheng CP Mao ZP Yan Y Xu YT Zhu YC Abashian A Gotow K Kajino F Low E Naito F Piilonen L Childers R Darden C Lusin S Rosenfeld C Wilson S Frautschi M Kagan H Kass R Trahern CG Ko W Lander RL Maeshima K Malchow RL Higashi JR Kurihara Y Maki A Nozaki T Omori T Perez P Sagawa H Sakai Y Sugimoto Y Takaiwa Y Terada S Tsuchiya K Poling R Green J Park IH Sakamoto S Sannes F Schnetzer S Stone R Trentalange S Zimmerman D Miyano K Miyata H 《Physical review letters》1988,61(8):911-914
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K Ogawa M Nishii J Inagaki F Nohara T Saito T Itaya T Fujii 《Chemical & pharmaceutical bulletin》1992,40(5):1315-1317
The synthesis of 8-methylguanine 7-oxide (3) was accomplished via a "phenacylamine route", which started from condensation of alpha-(4-methoxybenzylamino)propiophenone (6), prepared by coupling of alpha-bromopropiophenone (4) and 4-methoxybenzylamine (5), with 2-amino-6-chloro-5-nitro-4(3H)-pyrimidinone (7) and proceeded through cyclization of the resulting phenacylaminopyrimidinone (8) and removal of the 4-methoxybenzyl group. The N-oxide 3 and its 9-arylmethyl derivatives 9 and 11 showed only very weak antileukemic activity and no antimicrobial activity. 相似文献
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Abstract— A new method of using hydroxylamine as the reagent was developed to determine the concentrations of chlorophylls a and b in plant extracts accurately and sensitively. The method is based on the principle that hydroxylamine reacts in a short time with the aldehyde group of chlorophyll b in 95 per cent methanol at pH 5.8 to afford a derivative having a red band similar in position to the red band of chlorophyll a , while the spectrum of chlorophyll a is unaffected by the treatment with hydroxylamine. The method includes the measurements of absorbanlce for the mixture of a plant extract with hydroxylamine and for the reagent blank at a single wavelength, 666 mμ, and the concentrations of chlorophylls a and b are calculated from the absorbance value for the reagent blank and the increment of absorbance due to the reaction. By measuring this increment directly by difference photometry, one can determine a low concentration of chlorophyll b relative to chlorophyll a . The contents of chlorophylls in matured and etiolated leaves were determined by the method, and the errors included in this method were shown to be smaller than those in a commonly used technique including the measurements at two different wavelengths. 相似文献
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Synthesis and structures of the title compounds 2a–d are described. In spite of non-parallel orientation of the two base rings, fairly large hypochromism was observed for 2a–d. 相似文献
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The hydrothermal syntheses of the alkali metal molybdenum bronzes from starting solids (HxMoO3) with structural affinities to the desired products were investigated. Single-phase potassium blue and red bronzes were prepared by the hydrothermal treatments at around 430 K, and characterized by powder X-ray diffraction, IR spectroscopy, and SEM. The formation processes of these two bronzes during the hydrothermal treatments were found to differ. The blue bronze was formed by a structure-inheriting solid-state route from HxMoO3 with x<0.3, whereas the red bronze was formed for x>0.3 through a solution dissolution/deposition route via the formation of MoO3+MoO2. 相似文献