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71.
Hayashi Y Obata N Tamaru M Yamaguchi S Matsuo Y Saeki A Seki S Kureishi Y Saito S Yamaguchi S Shinokubo H 《Organic letters》2012,14(3):866-869
A biphenyl-fused BODIPY was synthesized through a facile oxidative cyclization of peripheral aryl-substituents at the β-position of the BODIPY unit. The extended π-system of the fused BODIPY induces near-infrared (NIR) absorption and strong π-π interactions in the solid state. These features are beneficial for the application of the dye as a functional material. The biphenyl-fused BODIPY dye was demonstrated to exhibit photocurrent conversion ability on the basis of its n-type semiconducting property. 相似文献
72.
Kamagata K Kawaguchi T Iwahashi Y Baba A Fujimoto K Komatsuzaki T Sambongi Y Goto Y Takahashi S 《Journal of the American Chemical Society》2012,134(28):11525-11532
A method was developed to detect fluorescence intensity signals from single molecules diffusing freely in a capillary cell. A unique optical system based on a spherical mirror was designed to enable quantitative detection of the fluorescence intensity. Furthermore, "flow-and-stop" control of the sample can extend the observation time of single molecules to several seconds, which is more than 1000 times longer than the observation time available using a typical confocal method. We used this method to scrutinize the fluorescence time series of the labeled cytochrome c in the unfolded state. Time series analyses of the trajectories based on local equilibrium state analysis revealed dynamically differing substates on a millisecond time scale. This system presents a new avenue for experimental characterization of the protein-folding energy landscape. 相似文献
73.
Hirotaka Ogawa Akinori Kan Norihiro Ikeda Akihiro Fujita 《Physica B: Condensed Matter》2012,407(21):4308-4312
The effect of In doping on the electroluminescence (EL) properties of Zn2SiO4:In thin films was investigated. In-doped Zn2SiO4 thin films were deposited on BaTiO3 substrates and their EL properties were characterized in this study. X-ray powder diffraction patterns of In-doped Zn2SiO4 powders revealed a single phase of Zn2SiO4 for In concentrations up to approximately 1.5 mol%, whereas a secondary phase of In2O3 was observed for In concentrations in the range of 2–10 mol%. The maximum luminance of thin film electroluminescent (TFEL) devices varied significantly with the amount of In doping. The highest luminance with blue emission was obtained when 2 mol% In was doped. The blue emission of In-doped Zn2SiO4 thin film may be related to the In substitution for Zn. The 2 mol% In-doped Zn2SiO4 thin film exhibited blue emission with CIE color coordinates of x=0.208 and y=0.086. 相似文献
74.
Seiya Tanaka Tsuneaki Sakurai Yoshihito Honsho Dr. Akinori Saeki Prof. Dr. Shu Seki Dr. Kenichi Kato Prof. Dr. Masaki Takata Prof. Dr. Atsuhiro Osuka Prof. Dr. Takuzo Aida 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(34):10554-10561
In contrast with their dimeric homologue, triply fused zinc porphyrin trimer–pentamer, as extra‐large π‐extended mesogens, assemble into columnar liquid crystals (LCs) when combined with 3,4,5‐tri(dodecyloxy)phenyl side groups ( 3 PZn – 5 PZn , Figure 1 ). Their LC mesophases develop over a wide temperature range, namely, 41–280 °C (on heating) for 5 PZn , and all adopt an oblique columnar geometry, typically seen in columnar LC materials involving strong mesogenic interactions. These LC materials are characterized by their wide light‐absorption windows from the entire visible region up to a near infrared (NIR) region. Such ultralow‐bandgap LC materials are chemically stable and serve as hole transporters, in which 5 PZn gives the largest charge carrier mobility (2.4×10?2 cm V?1 s?1) among the series. Despite a big dimensional difference, they coassemble without phase separation, in which the resultant LC materials display essentially no deterioration of the intrinsic conducting properties. 相似文献
75.
Tatsuya Oshima Akinori Suetsugu Yoshinari Baba Yuka Shikaze Keisuke Ohto Katsutoshi Inoue 《Journal of membrane science》2008
The present study examined the liquid membrane transport of the cationic protein cytochrome c, using the macrocyclic compound calix[6]arene, which is a carboxylic acid derivative, as a carrier. The transport rate was governed by carrier concentration and the pH gradient between the feed and the receiving phases, as well as the salt concentration in the aqueous phases. Transport of cytochrome c was examined using a series of calix[n]arene carboxylic acid derivatives (n = 4, 6 and 8). Cytochrome c successfully permeated membranes in the presence of the calix[6]arene derivative. Liquid membrane separation of cytochrome c from a mixture of cationic proteins was demonstrated under optimal conditions. Cytochrome c was selectively extracted by the calix[6]arene carboxylic acid derivative and 77% of the extracted cytochrome c was recovered into the receiving phase. In this liquid membrane system, which discriminates between the number of lysine residues on the surface of proteins, cationic proteins with similar molecular weights and pIs were separated with macrocyclic compounds. 相似文献
76.
77.
A synthesis of an advanced ABCDE ring system (24c) having characteristic substituents in both benzene rings of ecteinascidin marine natural products is described based on our model studies. 相似文献
78.
Soamwadee Chaianansutcharit Rangson Katsutath Aticha Chaisuwan Thallada Bhaskar Akio Nigo Akinori Muto Yusaku Sakata 《Journal of Analytical and Applied Pyrolysis》2007,80(2):360-368
Degradations of polypropylene (PP) and polyethylene (PE) over pure hexagonal mesoporous silica and aluminum-containing hexagonal mesoporous silica catalysts were studied in a fixed bed catalytic reactor at 380 and 430 °C, respectively. The thermal and catalytic degradations of both PP and PE in liquid-phase-contact and vapor-phase-contact modes over pure hexagonal mesoporous silica had no significant effect on the product yields. The liquid products were widely distributed in hydrocarbons with boiling point ranges of 36–405 °C. By adding a small amount of aluminum to the hexagonal mesoporous material, aluminium-containing hexagonal mesoporous silica exhibited good performance in cracking heavy molecular weight hydrocarbons into light hydrocarbons. High liquid yields and less coke deposits were obtained in liquid-phase-contact reaction with increasing aluminum content. The liquid products were mainly composed of C5–C10 hydrocarbons with boiling points of 36–174 °C, and propene, butene, and butane were main components in gaseous products. The effect of degradation temperature was not observed on product yields though degradation rate of polyolefin into liquid products was faster. Conversely, in vapor-phase-contact reaction, an increase in gaseous yield was observed when increasing the amount of aluminum and temperature of the cracking reactor, while the residue yield remained constant. 相似文献
79.
Higashi T Yamauchi A Shimada K Koh E Mizokami A Namiki M 《Analytical and bioanalytical chemistry》2005,382(4):1035-1043
A practical liquid chromatography–tandem mass spectrometric (LC-MS-MS) method for the determination of prostatic 5-dihydrotestosterone (DHT) and testosterone (T) has been developed. The prostatic androgens were extracted with MeOH–H2O (3: 7, v/v), purified with an Oasis HLB cartridge, derivatized with the permanently charged reagent 2-hydrazino-1-methylpyridine (HMP), and subjected to LC–MS-MS analysis using electrospray ionization (ESI) operated in the positive ion mode. The derivatization with HMP was very effective at increasing the detectability using the positive-ESI-MS. The method allowed the reproducible and accurate quantification of ng g–1 tissue levels of prostatic androgens in 10 mg of tissue. That is, the intra- and inter-assay coefficients of variation were below 8.1 and 9.3%, respectively, and the analytical recoveries of the androgens were quantitative. The limits of quantitation for DHT and T were both 1.0 ng g–1 tissue. The developed method was used to determine DHT and T in the prostates of patients with benign prostatic hyperplasia and prostate cancer, and satisfactory results were obtained. 相似文献
80.
Exposure of dilute solution of bromobenzene and p-dibromobenzene in fluorotrichloromethane to 60Coγ-rays at 77 K gave the corresponding cations characterized by ESR spectra. Estimated spin densities on bromine of ≈ 30% and 23%, respectively, are greater than those predicted by comparison with neutral α-bromo radicals, R2CBr (≈ 15%). Evidence for dimer cation formation in more concentrated solutions is presented. 相似文献