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81.
A novel oxidative cyclization of quinone-arenols 5 leading to products 6 with a dibenzofuran-1,4-dione structure, which forms the core of several natural products, has been developed and applied to the synthesis of violet-quinone (4). 相似文献
82.
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84.
Dragan Manasijevi? Duško Mini? Iwao Katayama Desimir Petkovi? 《Journal of Physics and Chemistry of Solids》2009,70(9):1267-1273
Binary thermodynamic data, successfully used for phase diagram calculations of binary systems Bi-Ga, Bi-Sn, and Ga-Sn, were used for prediction of phase equilibria in ternary Bi-Ga-Sn system. The thermodynamic functions, such as enthalpy of formation and activity, were calculated using the Redlich-Kister-Muggianu model and compared with experimental data reported in the literature. The liquidus surface, invariant equilibria and three vertical sections with molar ratio Ga:Sn=1, Bi:Sn=1 and Bi:Ga=1 of the Bi-Ga-Sn ternary system were calculated by the CALPHAD method. Alloys, situated along three calculated vertical sections, were investigated by Differential Scanning Calorimetry (DSC). The experimentally determined phase transition temperatures were compared with calculation results and good mutual agreement was noticed. 相似文献
85.
Synthetic studies of two components of tubulysins, tubulin polymerization inhibitors are described. The highly stereoselective synthesis of tubuvaline methyl ester (2) was accomplished by 1,3-dipolar cycloaddition of nitrone d-6 and acrylic acid derivatives 7 as a key step. The synthesis of tubuphenylalanine (3) was conducted by an aldol reaction of a boron enolate of (S)-4-isopropyl-3-propionyl-2-oxazolidinone (13) with aldehyde 14, readily prepared from phenylalanine, followed by Barton deoxygenation under radical conditions. 相似文献
86.
Zhang GJ Song KS Nakamura Y Ueno T Funatsu T Ohdomari I Kawarada H 《Langmuir : the ACS journal of surfaces and colloids》2006,22(8):3728-3734
We report a novel method of one-step direct amination on polycrystalline diamond to produce functionalized surfaces for DNA micropatterning by photolithography. Polycrystalline diamond was exposed to UV irradiation in ammonia gas to generate amine groups directly. After patterning, optical microscopy confirmed that micropatterns covered with an Au mask were regular in size and shape. The regions outside the micropatterns were passivated with fluorine termination by C3F8 plasma, and the chemical changes on the two different surfaces--the amine groups inside the patterned regions by one-step direct amination and fluorine termination outside the patterned regions--were characterized by spatially resolved X-ray photoelectron spectroscopy (XPS). The patterned areas terminated with active amine groups were then immobilized with probe DNA via a bifunctional molecule. The sequence specificity was conducted by hybridizing fluorescently labeled target DNA to both complementary and noncomplementary probe DNA attached inside the micropatterns. The fluorescence micropatterns observed by epifluorescence microscopy corresponded to those imaged by optical microscopy. DNA hybridization and denaturation experiments on a DNA-modified diamond show that the diamond surfaces reveal superior stability. The influence of a different amination time on fluorescence intensity was compared. Different terminations as passivated layers were investigated, and as a result, fluorine termination points to the greatest signal-to-noise ratio. 相似文献
87.
Kashimoto K Takata Y Matsuda T Ikeda N Matsubara H Takiue T Aratono M Tanida H Watanabe I 《Langmuir : the ACS journal of surfaces and colloids》2006,22(20):8403-8408
The total-reflection X-ray absorption fine structure (XAFS) method previously employed for the adsorption of dodecyltrimethylammonium bromide (DTAB) at the air/water interface was applied to that in the presence of NaBr. The surface concentration of the bromide ions Gamma(X)(B) of DTAB and NaBr was evaluated by using the Br K-edge absorption jump values of the total-reflection XAFS spectra and was compared to the corresponding value Gamma(H)(B) estimated from the dependence of surface tension on the bulk concentrations of DTAB m(1) and NaBr m(2). The Gamma(X)(B) values trace almost perfectly the Gamma(X)(B) versus m(1) curve up to a concentration near the critical micelle concentration (cmc) and deviate gradually above the concentration. This behavior is basically similar to that of the single DTAB system and ensures that the XAFS method is also applicable to the DTAB system, even in the presence of NaBr. In addition, this method was extended to the single nonionic amphiphile with covalently bonded bromine, and the surface concentrations of 6-bromo-1-hexanol (BrC6OH), Gamma(X)(1) and Gamma(H)(B), were evaluated and compared with each other. It was found that the Gamma(X)(1) value almost perfectly traces the Gamma(H)(1) versus m(1) curve, even at high surface concentrations. The excellent coincidence confirmed that the total-reflection XAFS method can be applied to the nonionic amphiphile system as well as a cationic surfactant with or without an added salt system. Finally, the difference between the Gamma(X)(B) and Gamma(H)(B) values observed in the DTAB with and without an added salt system is briefly described. 相似文献
88.
Aida H Mori K Yamaguchi Y Mizuta S Moriyama T Yamamoto I Fujimoto T 《Organic letters》2012,14(3):812-815
A phosphinite derivative that can be easily prepared in two steps from commercially available aminoindanol was found to be an effective catalyst for enantioselective acylation of diols. For the asymmetric desymmetrization of meso-1,2-diols, the corresponding monoester was obtained in up to 95% ee from the reaction in the presence of 5 mol % catalyst. 相似文献
89.
Iwao Soga Steve Granick 《Colloids and surfaces. A, Physicochemical and engineering aspects》2000,170(2-3):113-117
We measure, for the first time, the separate surface coverage-dependent orientations of trains and of loops/tails in the structure of an adsorbed polymer, and show that these have different average orientations. The system was PMMA (atactic polymethylmethacrylate) adsorbed onto oxidized silicon from dilute solution in carbon tetrachloride at 25.0°C. The method was FTIR-ATR (infrared spectroscopy in attenuated total reflection). With increasing surface coverage, train segments were observed to maintain constant average anisotropy with respect to the solid surface. Free segments were preferentially flattened when the surface coverage was low, but with increasing surface coverage became progressively more random in orientation. Free and bound segments were separated according to shifts of the vibrational frequencies of carbonyl segments upon hydrogen-bonding to the surface silanol groups. The dependence of segmental orientation on molecular weight of the chain is also discussed. 相似文献
90.
Yu Matsuda Hideo Mori Yoshiki Sakazaki Toru Uchida Suguru Suzuki Hiroki Yamaguchi Tomohide Niimi 《Experiments in fluids》2009,47(6):1025-1032
Pressure-sensitive paint (PSP) has the potential as a diagnostic tool for pressure measurement in high Knudsen number regime
because it works as a so-called “molecular sensor”. However, there are few reports concerning application of PSP to micro-devices,
because conventional PSPs are too thick owing to polymer binders. In our previous work, we adopted the Langmuir–Blodgett (LB)
technique to fabricate the pressure-sensitive molecular film (PSMF) using Pd(II) Mesoporphyrin IX (PdMP), which has pressure
sensitivity only in the low pressure range (below 130 Pa). In this study, aiming for pressure measurement under an atmospheric
pressure condition, we have constructed four samples of PSMFs composed of Pt(II) Mesoporphyrin IX (PtMP), Pt(II) Mesoporphyrin
IX dimethylester (PtMPDME), Pt(II) Protoporphyrin IX (PtPP) and Cu(II) Mesoporphyrin IX dimethylester (CuMPDME) as luminescent
molecules. The pressure sensitivity of those PSMFs was measured, and it was clarified that the pressure sensitivity of PSMF-PtMP
is the highest among the four samples. Moreover, the temperature dependency of PSMF-PtMP was investigated, and we found that
the temperature dependency of PSMF is dominated not by the oxygen diffusion in the layer, but by non-radiative deactivation
process of excited luminescent molecules. 相似文献