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71.
Jun Oshitani Shiho Takashina Mikio Yoshida Kuniaki Gotoh 《Colloids and surfaces. A, Physicochemical and engineering aspects》2009,350(1-3):136-140
The objective of this study is to estimate the contribution of Na+ as a counterion in the formation of H-AOT&Na-AOT-based W/O microemulsions using aqueous NaOH solution by pyranine absorbance measurements. A mixture of an aqueous NaOH solution containing pyranine/H-AOT&Na-AOT/isooctane was emulsified by changing the mixing ratio of Na-AOT (XNa-AOT = 0–1) and the mole fraction of NaOH (XNaOH = [NaOH]/the AOT− concentration in the water pool = 0–1). The phase behavior of the emulsified mixture was evaluated from the absorbance of pyranine at the isosbestic point and by visual observations. W/O microelumsions are formed at the mid-range of XNa-AOT, whereas the emulsified mixture separates into two phases at lower XNa-AOT and higher XNa-AOT. The two phase boundaries shift toward lower XNa-AOT as with increasing XNaOH. The phase behavior depends on the degree of screening of electrostatic repulsions between the polar headgroups of AOT− by the Na+ counterion. Interestingly, nano-sized W/O microemulsions are formed without phase separation using a highly concentrated NaOH aqueous solution when the Na-AOT mixing ratio is appropriately adjusted. The phase behavior was plotted as XNaOH versus XNa-AOT, and the correlation equations for the two phase boundaries were obtained by fitting the points. The contribution of the Na+ counterion from NaOH to W/O microemulsion formation was estimated by the correlation equations. The absorbance of pyranine and the size of W/O microemulsions, as measured by DLS, were plotted as a function of XNa+=(x[Na+ from NaOH]+[Na+ from Na-AOT])/[AOT−], in which x is the ratio contributed by NaOH. The absorbance and size correlates well with XNa+, indicating that XNa+ is a meaningful parameter for quantitatively estimating phase behavior and size variation. 相似文献
72.
We have been developing a combination method for environmental TEM (E-TEM) and phase-plate TEM (P-TEM) that enables direct observations of the structure of biological molecules in aqueous solution. It is clearly demonstrated that the biological molecules in a water layer can be imaged by the combined method without any stain. The spatial resolution obtained in the present study was about 10nm. This should be improved by using energy filtering. The image contrast of the specimen in water was reduced in comparison with that in vacuum. A model calculation that includes the effects of beam broadening, intensity decrease, and background increase caused by scattering from the water layer around the specimen shows that an increase in the thickness of the water layer reduces the contrast, intensity, and resolution of the image. 相似文献
73.
Yang J Ichii T Murase K Sugimura H 《Langmuir : the ACS journal of surfaces and colloids》2012,28(20):7579-7584
We have fabricated gold nanoparticle (AuNP) arrays on indium-tin oxide (ITO) substrates in a nearly one-dimensional fashion. AuNPs were site-selectively immobilized on ITO of which the surface had been patterned by a nanolithography process based on scanning probe microscopy. The fabricated nanoscale lines covered with aminosilane self-assembled monolayer served as chemisorption sites for citrate-stabilized AuNPs of 20 nm in diameter, accordingly, AuNP nanolines with a thickness of single nanoparticle diameter were spontaneously assembled on the lines. In this 1D array, the AuNPs were almost separated from each other due to the electrostatic repulsion between their negatively charged surface layers. Furthermore, a reorganization process of the immobilized AuNP arrays has been successfully demonstrated by replacing each AuNP's surface layer from citric acid to dodecanethiol. By this process, the AuNPs lost their electrostatic repulsion and became hydrophobic so as to be attracted to each other through hydrophobic interaction, resulting in reorganization of the AuNP array. By repeating the deposition and reorganization cycle, AuNPs were more densely packed. The optical absorption peak of the arrays due to their plasmonic resonance was found to shift from 526 to 590 nm in wavelength with repeating cycles, indicating that the resonance manner was changed from the single nanoparticle mode to the multiple particle mode with interparticle coupling. 相似文献
74.
Kuniaki Tatsuta Tomohiro Fukuda Tatsuya Ishimori Rearu Yachi Shinpei Yoshida Hiroshi Hashimoto Seijiro Hosokawa 《Tetrahedron letters》2012,53(4):422-425
The first total synthesis of hibarimicinone has been achieved. The polyhydroxydecalin moieties (AB and GH rings) have been synthesized from sulfonylenone 4 derived from d-arabinose. The chiral biaryl 20 was coupled with two polyhydroxydecalins 11 by Michael–Dieckmann type condensation to give the eight rings system. Aromatization and oxidation with Ag+ gave quinone 24, and the subsequential transannular etheration gave the hibarimicinone skeleton. Deprotection and tautomerization were performed in one pot to give hibarimicinone (1). 相似文献
75.
Krishnamurthy V. V. Watanabe I. Nagamine K. Kitagawa J. Ishikawa M. Komatsubara T. 《Hyperfine Interactions》2001,136(3-8):385-389
Magnetic and quadrupolar ordering phenomena in a Ce3Pd20Ge6 single crystal have been investigated by muon spin rotation/relaxation (μ+SR) spectroscopy. We have observed spontaneous precession of muons in zero-field below T
N
=0.7 K in the antiferromagnetic state. The precession frequency follows the power law: ν(T)=ν(0)(1−T/T
N
)
n
. The exponent n=0.43(2) is close to the mean-field value of 0.5. The muon longitudinal spin relaxation rate 1/T
1 is found to be nearly independent of temperature in the range of 0.3 to 2 K, i.e., across either T
N
or T
Q
=1.2 K, the quadrupolar ordering temperature. Two likely mechanisms for the temperature independent behavior of 1/T
1 are suggested.
This revised version was published online in September 2006 with corrections to the Cover Date. 相似文献
76.
Scheicher R. H. Cammarere D. Briere T. M. Sahoo N. Das T. P. Pratt F. L. Nagamine K. 《Hyperfine Interactions》2001,136(3-8):755-758
The microscopic details of the electron transfer in cytochrome c (cyt c) are being investigated by the Muon Spin Relaxation
(μSR) technique. We are using the Hartree–Fock Cluster Procedure to determine the most likely trapping sites for μ+ and muonium (Mu) in the protein chain, and have performed extensive calculations in single amino acid molecules of the protein
chain of cyt c. The double-bonded oxygen atom of the carboxyl group was identified as the trapping site for both μ+ and Mu. Utilizing the wave functions we obtained from the Hartree–Fock calculations, we have determined the hyperfine field
that the μ+ in Mu experiences while the latter is trapped at the oxygen.
This revised version was published online in September 2006 with corrections to the Cover Date. 相似文献
77.
Jeong Junho Briere Tina M. Sahoo N. Das T. P. Ohira Seiko Nishiyama K. Nagamine K. 《Hyperfine Interactions》2001,136(3-8):769-775
The trapping sites for muon and muonium in ferromagnetic p-Cl–Ph–CH=N–TEMPO [(4-(p-chlorobenzylideneamino)–TEMPO (TEMPO = 2,6,6-tetramethyl-piperidin-1-yloxyl)]
and the hyperfine interaction tensors for these sites are obtained using first-principles Unrestricted Hartree–Fock theory.
The calculated hyperfine interactions are used to compare the calculated zero field muon spin rotation (μSR) frequencies for
different choices for the easy axis and the observed frequency. It has been concluded that the two trapping centers that can
best explain the observed μSR frequency are a trapped singlet muonium near the radical oxygen and a trapped muon site near
the chlorine. The direction of the easy axis also is determined to be the b-axis of the monoclinic lattice. This direction for the easy axis is confirmed by determining the direction of the distributed
magnetization in the molecular solid which leads to a minimum dipole–dipole interaction energy. The consequences of this agreement
for the easy axis direction by two independent procedures are discussed.
This revised version was published online in September 2006 with corrections to the Cover Date. 相似文献
78.
79.
80.
Kuniaki Horie 《Journal of Number Theory》1985,20(2):238-253
Some asymptotic relations existing among arithmetical invariants of abelian fields are proved. 相似文献