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71.
Stochastic equations indexed by negative integers and taking values in compact groups are studied. Extremal solutions of the equations are characterized in terms of infinite products of independent random variables. This result is applied to characterize several properties of the set of all solutions in terms of the law of the driving noise. 相似文献
72.
Takaaki Taguchi Masaki Yabe Hitomi Odaki Miki Shinozaki Mikko Metsä-Ketelä Takao Arai Susumu Okamoto Koji Ichinose 《Chemistry & biology》2013,20(4):510-520
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73.
Kô Takehara Takao Fujimori Kei Inagi Mari Kajiwara Yoshikazu Harata Kazuhisa Yoshimura 《Electroanalysis》2013,25(2):387-393
A square‐wave voltammetric method for the determination of boric acid in water has been described based on the new understanding of the electrochemical behavior of boric acid‐Azomethine H complexation. Salicylaldehyde and H‐acid were used as the starting materials of boric acid‐Azomethine H complex and their concentrations were optimized for boric acid determination in water. A glassy carbon electrode, instead of a conventional mercury electrode, was used in the measurement. The detection limit of the proposed method was 0.10 mg B dm?3. The proposed method was successfully used for boric acid determination in the water from a seawater desalination RO plant. 相似文献
74.
Masahiro Yodoshi Natsumi Ikeda Naoko Yamaguchi Mana Nagata Noriaki Nishida Kazuaki Kakehi Takao Hayakawa Shigeo Suzuki 《Electrophoresis》2013,34(22-23):3198-3205
We have identified novel CE conditions for the separation of 7‐amino‐4‐methylcoumarin‐labeled monosaccharides and oligosaccharides from glycoproteins. Using a neutrally coated capillary and alkaline borate buffer containing hydroxypropylcellulose and ACN, saccharide derivatives form anionic borate complexes, which move from the cathode to the anode in an electric field and are detected near the anodic end. Excess labeling reagents and other fluorescent products remain at the cathodic end. Fluorimetric detection using an LED as a light source enables determination of monosaccharide derivatives with good linearity between at least 0.4 and 400 μM, may correspond to 140 amol to 140 fmol. The lower LOD (S/N = 5) is only 80 nM in the sample solution (ca. 28 amol). The results were comparable to reported values using fluorometric detection LC. The method was also applied to the analysis of oligosaccharides that were enzymatically released from glycoproteins. Fine resolution enables profiling of glycans in glycoproteins. The applicability of the method was examined by applying it to other derivatives labeled with nonacidic tags such as ethyl p‐aminobenzoate‐ and 2‐aminoacridone‐labeled saccharides. 相似文献
75.
Ionic liquid crystals based on ionic complexation of tris(2‐aminoethyl)amine (1) with 3,4,5‐tris(7,7,8,8,9,9,10,10,11,11,12,12,12‐tridecafluorododecyloxy)benzoic acid (2) and with 3,4,5‐tris(2‐octyldodecyloxy)benzoic acid (3) were investigated. The ionic complex with the partially fluorinated alkyl chains (1·2) exhibited a morphological transition from a hexagonal columnar mesophase to a Pm3n micellar cubic phase upon increasing the molar ratio of 2 to 1. For the complex with the branched alkyl chains (1·3) a micellar cubic mesophase was exclusively generated at appropriate composite ratios. The generation of the micellar cubic mesophases is attributed to the introduction of the laterally expanded volume of the alkyl chains compared with the corresponding normal dodecyl chains. Their thermal stabilities were most enhanced at a specific molar ratio of 1:5 for 1·2 and 1:4 for 1·3. This result corresponds to the most suitable chain volume for the stable micellar cubic mesophase. 相似文献
76.
NMR and DFT studies on persistent carbocations derived from benzo[kl]xanthene,dibenzo[d,d′]benzo[1,2‐b:4,3‐b′]difuran,and dibenzo[d,d′]benzo[1,2‐b:4,5‐b′]difuran in superacidic media
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Takao Okazaki Madoka Nakagawa Takeshi Futemma Toshikazu Kitagawa 《Journal of Physical Organic Chemistry》2016,29(2):107-111
Persistent carbocations generated by the protonation of hetero‐polycyclic aromatic compounds with oxygen atom(s) were studied by experimental NMR and density function theory calculations. Benzo[kl]xanthene ( 1 ), dibenzo[d,d′]benzo[1,2‐b:4,3‐b′]difuran ( 2 ), and dibenzo[d,d′]benzo[1,2‐b:4,5‐b′]difuran ( 3 ) were synthesized by the annulation of arenediazonium salts. Compound 1 in FSO3H‐SbF5 (4:1)/SO2ClF and 3 in FSO3H‐SbF5 (1:1)/SO2ClF ionized to 1aH+ with protonation at C(4) and to 3aH+ with protonation at C(6), and these cations were successfully observed by NMR at low temperatures. The density function theory calculations indicated that 1aH+ and 3aH+ were the most stable protonated carbocations and that 2 should ionize to 2aH+ with protonation at C(6). According to the changes in 13C chemical shifts (Δδ13C), the positive charge was delocalized into the naphthalene unit for 1aH+ , into one benzo[b,d]furan unit for 2aH+ , and into one benzo[b,d]furan unit for 3aH+ . Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
77.
A polymeric multilayered mirror doped with a saturable dye worked as a passive Q-switch of a laser-diode-pumped Nd(3+):YVO4 microchip laser. The multilayered mirror consisted of alternately spin-coated layers of polyvinylcarbazole (PVK) and cellulose acetate on a glass substrate. A dye of bis-(dimethylaminodithiobenzil)-nickel was doped in one of the layers of PVK, providing the repetitively Q-switched pulses. The pulse width and repetition rate were 4 ns and 68 kHz, respectively, for a laser-cavity length of 5 mm, and the average and the peak power were 40 mW and 156 W, respectively, for the highest pump power of 435 mW. The dependence of the Q-switched characteristics on the pump power and on the concentration of the doped dye is described. 相似文献
78.
Kumar Samir Taneichi Taiga Fukuoka Takao Namura Kyoko Suzuki Motofumi 《Cellulose (London, England)》2021,28(17):10803-10813
Cellulose - Surface-enhanced Raman spectroscopy (SERS)-based biosensors have recently been extensively developed because of their high sensitivity and nondestructive nature. Conventional SERS... 相似文献
79.
Unsymmetrical Pincer‐Type Ruthenium Complex Containing β‐Protic Pyrazole and N‐Heterocyclic Carbene Arms: Comparison of Brønsted Acidity of NH Groups in Second Coordination Sphere
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Tatsuro Toda Prof. Dr. Shigeki Kuwata Prof. Dr. Takao Ikariya 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(31):9539-9542
A reaction of a 2‐(imidazol‐1‐yl)methyl‐6‐(pyrazol‐3‐yl)pyridine with [RuCl2(PPh3)3] resulted in tautomerization of the imidazole unit to afford the unsymmetrical pincer‐type ruthenium complex 2 containing a protic pyrazole and N‐heterocyclic carbene (NHC) arms. Deprotonation of 2 with one equivalent of a base led to the formation of the NHC–pyrazolato complex 3 , indicating that the protic NHC arm is less acidic. When 2 was treated with two equivalents of a base under H2 or in 2‐propanol, the hydrido complex 4 containing protic NHC and pyrazolato groups was obtained through metal–ligand cooperation. 相似文献
80.
Mapping Platinum Species in Polymer Electrolyte Fuel Cells by Spatially Resolved XAFS Techniques
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Dr. Shinobu Takao Dr. Oki Sekizawa Dr. Shin‐ichi Nagamatsu Dr. Takuma Kaneko Dr. Takashi Yamamoto Dr. Gabor Samjeské Dr. Kotaro Higashi Dr. Kensaku Nagasawa Dr. Takuya Tsuji Dr. Motohiro Suzuki Dr. Naomi Kawamura Dr. Masaichiro Mizumaki Prof. Dr. Tomoya Uruga Prof. Dr. Yasuhiro Iwasawa 《Angewandte Chemie (International ed. in English)》2014,53(51):14110-14114
There is limited information on the mechanism for platinum oxidation and dissolution in Pt/C cathode catalyst layers of polymer electrolyte fuel cells (PEFCs) under the operating conditions though these issues should be uncovered for the development of next‐generation PEFCs. Pt species in Pt/C cathode catalyst layers are mapped by a XAFS (X‐ray absorption fine structure) method and by a quick‐XAFS(QXAFS) method. Information on the site‐preferential oxidation and leaching of Pt cathode nanoparticles around the cathode boundary and the micro‐crack in degraded PEFCs is provided, which is relevant to the origin and mechanism of PEFC degradation. 相似文献