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排序方式: 共有195条查询结果,搜索用时 15 毫秒
41.
M. Hasegawa A. Kawasuso T. Chiba T. Akahane M. Suezawa S. Yamaguchi K. Sumino 《Applied Physics A: Materials Science & Processing》1995,61(1):65-70
We have measured positron lifetime and Two Dimensional Angular Correlation of Annihilation Radiation (2D-ACAR) distributions of Floating-Zone grown (FZ) Si specimens containing divacancies (V2) with the definite charge states, V
2
0
, V
2
–1
or V
2
–2
from room temperature to about 10 K. These charge states are accomplished by an appropriate combination of dopant species, their concentration and irradiation doses of 15 MeV electrons. with reference to the currently accepted ionization level of divacancies. The positron lifetime of the negatively charged divacancy increases with temperature, while that of the neutral divacancy shows little change with temperature. The positron trapping rate, obtained from lifetime and 2D-ACAR measurements, increases markedly with decreasing temperature. This is found not only for the negative divacancies but also for the neutral divacancy. We need a model which explains this temperature dependence. The 2D-ACAR distribution from positrons trapped at divacancies shows nearly the same distribution for the different charge states, which differs considerably from the case of As vacancies in GaAs studied by Ambigapathy et al. We have observed a small but definite anisotropy in the distribution of trapped positrons in V
2
–
using a specimen containing oriented divacancies.Paper presented at the 132nd WE-Heraeus-Seminar on Positron Studies of Semiconductor Defects, Halle, Germany, 29 August to 2 September 1994 相似文献
42.
Ariga K Urakawa T Michiue A Kikuchi J 《Langmuir : the ACS journal of surfaces and colloids》2004,20(16):6762-6769
As a novel category of two-dimensional lipid clusters, dendrimers having an amphiphilic structure in every unit were synthesized and labeled "spider-web amphiphiles". Amphiphilic units based on a Lys-Lys-Glu tripeptide with hydrophobic tails at the C-terminal and a polar head at the N-terminal are dendrically connected through stepwise peptide coupling. This structural design allowed us to separately introduce the polar head and hydrophobic tails. Accordingly, we demonstrated the synthesis of the spider-web amphiphile series in three combinations: acetyl head/C16 chain, acetyl head/C18 chain, and ammonium head/C16 chain. All the spider-web amphiphiles were synthesized in satisfactory yields, and characterized by 1H NMR, MALDI-TOFMS, GPC, and elemental analyses. Surface pressure (pi)-molecular area (A) isotherms showed the formation of expanded monolayers except for the C18-chain amphiphile at 10 degrees C, for which the molecular area in the condensed phase is consistent with the cross-sectional area assigned for all the alkyl chains. In all the spider-web amphiphiles, the molecular areas at a given pressure in the expanded phase increased in proportion to the number of units, indicating that alkyl chains freely fill the inner space of the dendritic core. The mixing of octadecanoic acid with the spider-web amphiphiles at the air-water interface induced condensation of the molecular area. From the molecular area analysis, the inclusion of the octadecanoic acid bears a stoichiometric characteristic; i.e., the number of captured octadecanoic acids in the spider-web amphiphile roughly agrees with the number of branching points in the spider-web amphiphile. 相似文献
43.
Transition metal complexes coordinated by an NAD(P)H model compound and their enhanced hydride-donating abilities in the presence of a base 总被引:1,自引:0,他引:1
Kobayashi A Konno H Sakamoto K Sekine A Ohashi Y Iida M Ishitani O 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(14):4219-4226
The ruthenium(II) and rhenium(I) complexes containing an NAD(P)H model compound, 1-benzyl-1,4-dihydronicotinamide (BNAH), as ligand, [Ru(tpy)(bpy)(BNAH)]2+ (1 a) and [Re(bpy)(CO)3(BNAH)]+ (1 b), were quantitatively produced by the reaction of the corresponding metal hydrido complexes with BNA(+) (1-benzylnicotinamidium cation). In the presence of base with pK(a) = 8.9, 1 a and 1 b have much greater reducing power than "free" BNAH. The oxidation potentials of 1 a in the absence and the presence of triethylamine were 0.55 V and -0.04 V, respectively, versus Ag/AgNO(3), whereas that of "free" BNAH was 0.30 V. Spectroscopic results clearly showed that the base extracts a proton from the carbamoyl group on 1 a and 1 b to give the deprotonated BNAH coordinating to the transition-metal complexes [Ru(tpy)(bpy)(BNAH-H+)]+ (3 a) and [Re(bpy)(CO)3(BNAH-H+)] (3 b); this deprotonation underlies the enhancement in reducing ability. The deprotonated forms 3 a and 3 b can efficiently reduce other NAD(P) models to give the corresponding 1,4-dihydro form, resulting in the deprotonated BNA+ being coordinated to the metal complexes [Ru(tpy)(bpy)(BNA(+)-H+)]2+ (2 a) and [Re(bpy)(CO)3(BNA+-H+)]+ (2 b); "free" BNAH and the protonated adducts 1 a and 1 b cannot act in this way. X-ray crystallography was performed on the PF6- salt of 2 a, and showed that the deprotonated nitrogen atom on the carbamoyl group coordinates to the ruthenium(II) metal center with a bond length of 2.086(3) Angstroms. Infrared spectral data suggested that the deprotonated carbamoyl group on the reduced forms 3 a and 3 b is converted to the imido group, and that the oxygen atom coordinates to the metal center. 相似文献
44.
45.
Enzymatic preparation of optically active silicon-containing amino acids and their application 总被引:2,自引:0,他引:2
Takuo Kawamoto Hayato Yamanaka Atsuo Tanaka 《Applied biochemistry and biotechnology》2000,88(1-3):17-22
Optically active 3-trimethyl silylalanine (TMS-Ala) was prepared by hydrolysis of N-acetyl-dl-TMS-Ala catalyzed by acylase I (aminoacylase; N-acylamino-acid amidohydrolase, EC3.5.1.14). Acylase I from porcine kidney (PKA) was found to be more effective than that
from Aspergillus melleus in the preparation of l-TMS-Ala. Under the optimized conditions, optically pure l-TMS-Ala (>99% enantiomeric excess, ee) was obtained with a 72% yield. Furthermore, a highly optically pure d-TMS-Ala (96% ee) could also be obtained with a 76% yield by chemical hydrolysis of the residual substrate. Enzymatic synthesis
of peptides containing TMS-Ala was also attempted in ethyl acetate. Benzyloxycarbonyl (Z)-l-TMS-Ala served as the substrate for thermolysin, whereas l-TMS-Ala-OMe was inactive as the amino component. In the case of inhibitory activity of dipeptides toward thermolysin, l-Leu-(l-TMS-Ala) was found to be a more potent inhibitor than l-Leu-l-Leu, which is known to be one of the most effective inhibitors of thermolysin among the dipeptides consisting of natural
aminoacids. 相似文献
46.
47.
Yoshio Kobayashi Takuya Nozawa Tomohiko Nakagawa Kohsuke Gonda Motohiro Takeda Noriaki Ohuchi Atsuo Kasuya 《Journal of Sol-Gel Science and Technology》2010,55(1):79-85
This paper describes a method for direct coating of fluorescent semiconductor nanoparticles with silica shell. The fluorescent
semiconductor nanoparticles used were CdSe
x
Te1–x
nanoparticles coated with ZnS and succeedingly surface-modified with carboxyl groups, or quantum dots (Q-dots). The Q-dots
were silica-coated by performing sol–gel reaction of tetraethyl orthosilicate (TEOS) using NaOH as a catalyst in the presence
of the Q-dots. Quasi-perfect Q-dots/silica core-shell particles were formed at 5.0 M H2O and 4.0 × 10−4 M NaOH. Under these concentrations of H2O and NaOH, the particle size of Q-dots/silica particles could be varied from 20.1 to 38.1 nm as the TEOS concentration increased
from 2.5 × 10−4 to 50 × 10−4 M. The Q-dots/silica particles showed fluorescence as well as the uncoated Q-dots. 相似文献
48.
Marine Cuisinier Jean-Frédéric Martin Nicolas Dupré Atsuo Yamada Ryoji Kanno Dominique Guyomard 《Electrochemistry communications》2010,12(2):238-241
The impact of air exposure on LiFePO4–C nanocomposites has been investigated at moderate temperature. We show here that the storage in 120 °C hot air for 30 days leads not only to the material delithiation but also to the formation of an amorphous ferric phosphate side-phase, accounting for 38% of the total iron. The formed phase is found to be partially hydrated, suggesting a water-driven aging mechanism and a proposed hypothetic formula: LixFePO4(OH)x. The side-phase displays new electrochemical activity but poor cyclability and the overall battery performance is thus deteriorated. The regeneration of pristine structure, together with the performance recovery can be achieved by a simple thermal treatment under inert atmosphere. 相似文献
49.
50.
Development of high-performance aqueous batteries is an important goal for energy sustainability owing to their environmental benignity and low fabrication costs. Although a layered vanadyl phosphate is one of the most-studied host materials for intercalation electrodes with organic electrolytes, little attention has been paid to its use in aqueous Li+ systems because of its excessive dissolution in water. Herein, by controlling the water concentration, we demonstrate the stable operation of a layered vanadyl phosphate electrode in an aqueous Li+ electrolyte. The combination of experimental analyses and density functional theory calculations reveals that reversible (de)lithiation occurs between dehydrated phases, which can only exist in an optimal water concentration.We demonstrate aqueous Li+ intercalation chemistry of vanadyl phosphate in the form of monohydrates, which are only stable in an optimal water-concentration environment. 相似文献