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51.
52.
Koga K Takekoshi K Kawashima S Taniguchi M Murakami M 《Chemical & pharmaceutical bulletin》2004,52(12):1507-1510
One persistent problem with using therapeutic concentrations of glycyrrhizin (GZ) is that, at these high concentrations, it forms a gel in an aqueous solution. We previously solved this problem by dissolving GZ in a highly concentrated phosphate buffer. Unfortunately, the resulting GZ solution has a hyperosmotic pressure that renders it unsuitable for use in patients. The aim of this study was to prepare a highly concentrated GZ solution having an osmotic pressure ratio of 1 and a pH of 7.4. By adding small amounts of oil and using a 100 mM phosphate buffer, we achieved an emulsified GZ solution that is stable at room temperature and has a physiological osmotic pressure and pH. When clove oil was used as an emulsifier, the gel formation temperature of GZ solution decreased appreciably compared to that of GZ solution without clove oil. Using scanning electron microscopy (SEM), we examined the detailed characteristics of GZ gels prepared from solutions with or without clove oil. SEM of cross sections of GZ gels revealed an irregular structure in gels prepared with clove oil, indicating that clove oil prevented the formation of the intermolecular GZ networks typically characterized by gels derived from pure GZ solutions. 相似文献
53.
Shirokawa S Kamiyama M Nakamura T Okada M Nakazaki A Hosokawa S Kobayashi S 《Journal of the American Chemical Society》2004,126(42):13604-13605
A highly regio- and diastereoselective TiCl4-mediated vinylogous Mukaiyama aldol reaction using the chiral vinylketene silyl N,O-acetal has been developed. The present vinylogous Mukaiyama aldol reaction provides a unique and effective means of controlling remote asymmetric induction. The methyl group at the alpha-position is important in achieving a high level of stereoselectivity. From a synthetic point of view, this methodology can provide a one-step construction of delta-hydroxy-alpha,gamma-dimethyl-alpha,beta-unsaturated carbonyl unit that is seen in many natural polyketide products. 相似文献
54.
Da-Bing Li Masakazu Aoki Hideto Miyake Kazumasa Hiramatsu 《Applied Surface Science》2007,253(24):9395-9399
High-temperature (HT) AIN films were grown on (0 0 0 1) sapphire by low-pressure flow-modulated (FM) metal organic vapor phase epitaxy (MOVPE) with and without inserting a thin medium-temperature (MT) AIN layer. To suppress parasitic reactions between the sources of trimethylaluminum (TMA) and ammonia (NH3), TMA and NH3 was introduced to the reactor of MOVPE by alternating supply way. Surface morphology and crystalline quality were characterized by a scanning electronic microscopy (SEM), atomic force microscopy (AFM) and X-ray rocking curve (XRC) measurements of (0 0 0 2) and (10-12) diffractions. The AFM and SEM measurements indicated that the thin MT-AIN layer had a strong influence on the surface morphology of the HT-AIN films. The surface morphology became quite smooth by inserting the thin MT-AIN layer and surface RMS roughness values were 0.84 nm and 13.4 nm for the HT-AIN films with and without inserting the thin MT-AIN buffer layer, respectively. By etching the samples in aqueous KOH solution, it was found that the polarity of AIN films was different, the HT-AIN film with the thin MT-AIN layer could not be etched, indicating that the film had an Al-polar surface; however, the film without the MT-AIN layer was etched, which was explained that that film had a N- or mixed-polar surface. The mechanism for the origin of the different polarity of HT-AIN with and without the thin MT-AIN layer was proposed and discussed in detail. 相似文献
55.
Masakazu Nakanishi Tomoko Ogi Yoshio Fukuda 《Journal of Thermal Analysis and Calorimetry》2010,101(1):391-396
We modified a commercially available thermogravimetric analyzer to introduce helium alone or with steam, oxygen or both, atmosphere
of which was controllable to be similar to that in a fixed-bed or an entrained-flow type gasifier, for studying basic properties
of biomass gasification. We also connected it to a gas chromatograph-mass selective detector for identifying materials produced
during the thermogravimetric analyses. Thermogravimetric analyses of Japanese cedar wood and identifications of the produced
materials at around 365 °C were measured as demonstrations. 相似文献
56.
Masakazu Yoshikawa Takashi Yukoshi Kohei Sanui Naoya Ogata 《Journal of polymer science. Part A, Polymer chemistry》1986,24(7):1585-1597
Separation of water–ethanol mixture through a membrane was carried out by pervaporation using a membrane which provided a hydrogen-bonding interaction. A membrane obtained from poly(acrylic acid-co-acrylonitrile) was effective for a selective separation of water from aqueous ethanol solution by pervaporation technique. Spectroscopic and flux analyses verified that this high selectivity toward water was attributed to the hydrogen-bonding interaction between water and acrylic acid (carboxylic acid) unit in the membrane. On the other hand, a membrane from poly(acrylic acid-co-styrene) preferentially permeated ethanol in the low water feed concentration region. 相似文献
57.
The palladium‐catalyzed reaction of acid anhydrides with silacyclobutane gives a mixture of cyclic silyl enol ether, carboxy(propyl)silane, and 3‐(carboxysilyl)ketone. In the presence of N,N‐dicyclohexylcarbodiimido (DCC), the reaction preferentially provides a cyclic silyl enol ether in a good yield. In addition, the palladium‐catalyzed reaction of benzoic acid with silacyclobutane in the presence of two equivalents of DCC also affords a cyclic silyl enol ether in a moderate yield. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
58.
Masafumi Yano Yorichika Okino Yuji Ichihara Masakazu Tatsumi Munetaka Oyama Kazunobu Sato Takeji Takui 《Polyhedron》2009,28(9-10):1764-1767
Three highly π-extended tetraaryl-1,3-phenylenediamines for charged high-spin molecular systems were successfully synthesized using Suzuki coupling. Their electrochemical and spectroscopic properties were also examined. They showed blue fluorescence. The dications derived from highly π-extended tetraaryl-1,3-phenylenediamines were generated and characterized by electron transfer stopped-flow method. 相似文献
59.
Kazuhiro Kobayashi Sunyoung Kim Masakazu Kojima 《Applied Mathematics and Optimization》2008,58(1):69-88
Exploiting sparsity has been a key issue in solving large-scale optimization problems. The most time-consuming part of primal-dual
interior-point methods for linear programs, second-order cone programs, and semidefinite programs is solving the Schur complement
equation at each iteration, usually by the Cholesky factorization. The computational efficiency is greatly affected by the
sparsity of the coefficient matrix of the equation which is determined by the sparsity of an optimization problem (linear
program, semidefinite program or second-order cone program). We show if an optimization problem is correlatively sparse, then the coefficient matrix of the Schur complement equation inherits the sparsity, and a sparse Cholesky factorization
applied to the matrix results in no fill-in.
S. Kim’s research was supported by Kosef R01-2005-000-10271-0 and KRF-2006-312-C00062. 相似文献
60.
Kondo M Mates TE Fischer DA Wudl F Kramer EJ 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):17000-17012
Interfaces between phenylacetylene (PA) monolayers and two silicon surfaces, Si(111) and Si(100), are probed by X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy, and the results are analyzed using ab initio molecular orbital calculations. The monolayer systems are prepared via the surface hydrosilylation reaction between PA and hydrogen-terminated silicon surfaces. The following spectral features are obtained for both of the PA-Si(111) and PA-Si(100) systems: a broad π-π* shakeup peak at 292 eV (XPS), a broad first ionization peak at 3.8 eV (UPS), and a low-energy C 1s → π* resonance peak at 284.3 eV (NEXAFS). These findings are ascribed to a styrene-like π-conjugated molecular structure at the PA-Si interface by comparing the experimental data with theoretical analysis results. A conclusion is drawn that the vinyl group can keep its π-conjugation character on the hydrogen-terminated Si(100) [H:Si(100)] surface composed of the dihydride (SiH(2)) groups as well as on hydrogen-terminated Si(111) having the monohydride (SiH) group. The formation mechanism of the PA-Si(100) interface is investigated within cluster ab initio calculations, and the possible structure of the H:Si(100) surface is discussed based on available data. 相似文献