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101.
Kim Gun Gyun Lee Jun Young Choi Pyeong Seok Vyas Chirag K. Yang Seung Dae Hur Min Gu Park Jeong Hoon 《Journal of Radioanalytical and Nuclear Chemistry》2018,316(3):1099-1106
Journal of Radioanalytical and Nuclear Chemistry - Accumulation of triphenylphosphonium (TPP) is normally observed in the mitochondria from the extracellular spaces due to the high difference in... 相似文献
102.
The design variable tolerance effects on the natural frequency variance of constrained multi-body systems in dynamic equilibrium are investigated in this study. Monte-Carlo simulation is often employed for such investigations, but it is known to have serious drawbacks. Excessive amount of computation time needs to be consumed since a large number of evaluations are usually required for the method. Furthermore, the solution accuracy cannot be always guaranteed in spite of the excessive amount of computation time. In order to overcome such drawbacks, a method employing eigenvalue sensitivity information is proposed to obtain the variance of natural frequency in this study. In order to verify the accuracy and the efficiency of the method, some numerical examples of multi-body systems in dynamic equilibrium are solved and the results are compared to those obtained by an analytical method and Monte-Carlo simulation. 相似文献
103.
Poly(ethylene glycol)‐crosslinked multimeric C60 was developed for use in photothermal/photodynamic therapy of malignant cells. We showed that: (i) the tumor surface temperature on KB tumor‐bearing nude mice treated with multimeric C60 reached about 44 °C; (ii) this hyperthermic condition and tremendous singlet oxygen generation from multimeric C60 resulted in significant tumor volume regression in KB tumor‐bearing nude mice; and (iii) multimeric C60 also efficiently inhibited arthritic progress in the arthritis‐induced DBA/1 J mice model. This multimeric C60 may be useful for photothermal/photodynamic cell ablation in various malignant cells. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
104.
Characterization of Nitro-Substituted Polybenzimidazole Synthesized by the Reaction with Nitric Acid
Abstract Nitro-substituted poly[2,2′-(m-phenylene)-5,5′-bibenzimidazole]s (PBIs) were synthesized by the reaction of PBI with nitric acid in sulfuric acid under various conditions. The number of nitro groups substituted on the aromatic ring of PBI per polymeric unit varied from 1.44 to 3.55 according to the reaction conditions. An increase in reaction temperature and concentration of the nitric acid increased the degree of substitution. The inherent viscosity of the substituted polymer increased as the reaction temperature decreased. When the reaction temperature was 30°C, the inherent viscosity of the polymer increased as the concentration of nitric acid increased. The nitro-substituted PBI exhibited polyelectrolyte behavior in formic acid. The nitro groups substituted on PBI were dissociated when the polymer was heated to 450°C, displaying exothermic behavior, and the decomposition of polymer was proportional to its nitro group content. All nitro-substituted PBIs showed better solubilities in polar aprotic and acidic solvents, such as dimethylacetamide, dimethylsulfoxide, dimethylformamide, N-methylpyrrolidone, formic acid, sulfuric acid, and trifluoromethanesulfonic acid. 相似文献
105.
Tae Seok Kwon Sadanori Kumazawa Shuji Kondo† Koji Takagi Hideo Kunisada Yasuo Yuki 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1895-1913
Abstract 1,4-Bis(p-tert-butylphenylselenomethyl) benzene was synthesized, and used as a bifunctional photoiniferter for the polymerization of styrene. Both the polymer yields and the number average of molecular weights (n) of polymers increased with the polymerization. The polymerization of styrene by this iniferter permitted telechelic polystyrene containing arylseleno groups at both chain ends, and the degree of functionality was 1.9. The seleno groups of both chain ends of polystyrene were reduced quantitatively by tri-n-butyltin hydride. These seleno groups in polystyrene were also eliminated by treatment with hydrogen peroxide to give telechelic polystyrene with carbon-carbon double bond at both chain ends. Further, polystyrene with double bonds was converted to telechelic polystyrene carrying terminal functional groups as epoxy, hydroxy, and iodide group, respectively. 相似文献
106.
A m-xylene bridged imidazolium receptor 1 has been designed and synthesized. The receptor 1 utilizes two imidazole (C–H)+—anion hydrogen bonds and one aromatic hydrogen—anion hydrogen bond. The major driving force of complexation between the receptor 1 and anions comes from two imidazole (C–H)+—anion hydrogen bonding. However, some hydrogen bonding energy between aromatic hydrogen and anion exists, although it is expected to be much smaller than that of imidazole (C–H)+—anion hydrogen bonds. 相似文献
107.
Richard A. Bartsch Takashi Hayashita Joung Hae Lee Jong Seung Kim Matthew G. Hankins 《Supramolecular chemistry》2013,25(3-4):305-311
Abstract Lipophilic crown ethers with pendent proton-ionizable groups are novel complexing agents for use in metal ion separations by solvent extraction. For a series of structurally related, lipophilic dibenzocrown ether carboxylic acids, the efficiency and selectivity of competitive alkali metal cation extraction for aqueous solution into chloroform is found to be strongly influenced by the crown ether ring size and the lipophilic group attachment site. Reaction of dibenzocrown ether carboxylic acids with formaldehyde in formic acid produces condensation polymers which possess both ion-exchange and cyclic polyether binding sites for metal ion complexation. These resins exhibit excellent exchange kinetics for competitive alkali metal cation sorption from aqueous solution and subsequent stripping and may be used in concentrator columns for the recovery of these metal ions from very dilute aqueous solution. Cation selectivity in the sorption and stripping steps is controlled by the structure of the crown ether monomer unit. 相似文献
108.
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110.
Sunwoong Bae Chul Woong Kim Jong Seob Choi Ji-Won Yang Tae Seok Seo 《Analytical and bioanalytical chemistry》2013,405(29):9365-9374
This study describes the development of a microfluidic device for the high-throughput screening of culture conditions, such as the optimum sodium acetate concentration for promoting rapid growth and high lipid accumulation of Chlamydomonas reinhardtii. An analysis of the microalgal growth on the microfluidic device revealed an optimum sodium acetate concentration of 5.72 g L?1. The lipid content, determined by the 4,4-Difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (BODIPY® 505/515) staining method, increased with the sodium acetate concentration. The results were found to be statistically reproducible with respect to cell growth and lipid production. Other nutrient conditions, including the nitrogen and phosphorus concentrations, can also be optimized on the same microfluidic platform. The microfluidic device performance results agreed well with the results obtained from the flask-scale experiments, validating that the culture conditions were scalable. Finally, we, for the first time, established a method for the absolute quantification of the microalgal lipid content in the picoliter culture volumes by comparing the on-chip and off-chip data. In conclusion, we successfully demonstrated the high-throughput screening of sodium acetate concentrations that induced high growth rates and high lipid contents in C. reinhardtii cells on the microfluidic device. Figure
We have developed a microfluidic device for the high-throughput screening of culture conditions for promoting rapid growth and high lipid accumulation of Chlamydomonas reinhardtii 相似文献