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101.
102.
Czesław Rudowicz Ireneusz Stefaniuk Roman Dziembaj Hitoshi Ohta Marcin Molenda Susumu Okubo Makoto Yoshida 《Research on Chemical Intermediates》2007,33(8):853-862
This paper deals with the analysis of the temperature dependence of high-frequency EMR (HF-EMR) spectra due to Mn3+ and Mn4+ ions in the lithium manganese spinel LiMn2O4. A range of powder samples obtained by the sol-gel method with calcinations in several temperature ranges were prepared for
this study. Based on the initial characterization carried out by a number of techniques, the physicochemical and structural
properties of the samples were earlier determined. Independently, temperature magnetization and HF-EMR measurements were carried
out. The EMR spectra vary strongly between samples, indicating possible structural or chemical changes. Quantitative analysis
of the temperature dependence of the HF-EMR spectra due to Mn3+ and Mn4+ ions in LiMn2O4 is presented in this paper. The spectral analysis concerns the line shape, linewidth, intensity and g-factors. Fittings using the Lorentzian spectral shape and, to a certain extent, the Gaussian spectral shape have been carried
out in order to parameterize the temperature dependence of the HF-EMR spectra. This parameterization of the HF-EMR experimental
data enables a deeper characterization of the samples. Subsequently, a better insight into the role of the Mn3+ and Mn4+ ions in accounting for the characteristics most suitable for application of LiMn2O4 as a cathode material may be gained. 相似文献
103.
通过萜品油烯和2,6-二氧代戊酸甲酯的de Mayo反应,使[2 + 2]环加成产物 3-6经retro-aldol重排,开环生成取代环己烯7和12。在不同反应介质中对开环产 物进行再环合,并对其反应机理进行研究。在碱性条件下,经分子内Claisen缩合 反应形成螺环化合物;以对甲本碘酸为催化剂的环合,除生成正常的Claisen缩合 产物以外,7和12均发生烯键亲核加成反应,生成具有二环[3.3.1]结构的桥环化合 物9-11和二环[3.2.1]结构的桥环化合物16-18。所得新化合物的化学结构均经IR, ~1H NMR,~(13)C NMR及元素分析予以确定。 相似文献
104.
Yoshitake T Ichinose F Yoshida H Todoroki K Kehr J Inoue O Nohta H Yamaguchi M 《Biomedical chromatography : BMC》2003,17(8):509-516
A highly sensitive, selective and simple method is described for the determination of histamine by high-performance liquid chromatography (HPLC) with fluorescence detection. The method is based on an intramolecular excimer-forming fluorescence derivatization of histamine with 4-(1-pyrene)butyric acid N-hydroxysuccinimide ester (PSE), followed by reversed-phase HPLC. Histamine, having two amino moieties in a molecule, was converted to the dipyrene-labeled derivative by reaction with PSE. The derivative afforded intramolecular excimer fluorescence (450-540 nm), which can clearly be discriminated from the monomer fluorescence (370-420 nm) emitted from PSE. Typically, a 10 micro L sample solution was mixed with 100 micro L of derivatization reagent solution, which was a mixture of 0.5 mm PSE in acetonitrile and 0.5 mm potassium carbonate in water (8:2, v/v). The derivatization was carried out at 100 degrees C for 90 min. The PSE derivative of histamine could be separated by reversed-phase ODS column with isocratic elution using acetonitrile:water (82:18, v/v) containing 0.03% triethylamine. The detection limit (singnal-to-noise ratio = 3) of histamine was 0.5 fmol for a 30 micro L injection. The method was successfully applied to the determination of histamine in human urine, and had enough selectivity and sensitivity for urinary histamine quantification. 相似文献
105.
Kawahara M Kabir MK Yamada K Adachi K Kumagai H Narumi Y Kindo K Kitagawa S Kawata S 《Inorganic chemistry》2004,43(1):92-100
Two new copper(II) compounds of chloranilate and 2,2':6',2' '-terpyridine have been synthesized, and the structures have been solved by the single-crystal X-ray diffraction method. The crystal structure of [[Cu(2)(CA)(terpy)(2)][Cu(CA)(2)]](n)(1), where H(2)CA = chloranilic acid and terpy = 2,2':6',2' '-terpyridine, consists of two modules, the dimer unit [Cu(2)(CA)(terpy)(2)](2+) and the anionic mononuclear unit [Cu(CA)(2)](2)(-), forming an alternated chain. The chain is stabilized by semicoordinating and additional but efficient secondary bonding interactions. The crystal structure of [[Cu(2)(CA)(terpy)(2)(dmso)(2)][Cu(CA)(2)(dmso)(2)](EtOH)](n)(2), where dmso = dimethyl sulfoxide, consists of solvent molecules and two discrete modules, the dimer unit [Cu(2)(CA)(terpy)(2)(dmso)(2)](2+) and the anionic mononuclear unit [Cu(CA)(2)(dmso)(2)](2)(-). The dimer units form a layer by secondary bonding interactions, and the monomer units and ethanol molecules are introduced between the layers. The magnetic properties of 1 and 2 have been investigated in the temperature range 2.0-300 K. A weak ferromagnetic interaction was observed in 1, J(a) = 2.36 cm(-)(1) and zJ(b) = -0.68 cm(-)(1) while no exchange coupling was observed in 2. 相似文献
106.
Yoshifumi Karakawa Kazuhiko Oka Hitoshi Odashima Kojiro Takagi Shozo Tsunekawa 《Journal of Molecular Spectroscopy》2001,210(2)
The rotational spectrum of methyl formate (HCOOCH3) has been observed in the frequency range from 7 to 200 GHz. We newly assigned 1612 lines in the ground torsional state and simultaneously analyzed both A- and E-species data including previously reported lines on the basis of the internal axis method. A total of 3077 lines were fitted to a 1σ standard deviation of 139 kHz, and molecular parameters were determined. 相似文献
107.
108.
Hitoshi Araki Kensuke Naka 《Journal of polymer science. Part A, Polymer chemistry》2012,50(20):4170-4181
Dumbbell‐shaped isobutyl‐substituted 1,2‐bis(4‐vinylphenyl)acetylene‐linked POSS (DA1), 9,10‐bis(4‐vinylphenyl)ethynyl)anthracene‐linked POSS (DA2), and 5,5″‐bis((4‐vinyl)phenyl)ethynyl)‐2,2′:5′2″‐terthiophene‐linked POSS (DA3), and corresponding model compounds were synthesized by cross metathesis and Sonogashira reaction, and their film formability, and thermal and optical properties were examined. The dumbbell structures of the obtained compounds were confirmed by 1H‐, 13C‐, and 29Si‐NMR and MALDI‐TOF‐MS analysis. The dumbbell‐shaped POSS compounds gave optically transparent films. All the model compounds, however, formed opaque films. All the films were emissive under UV irradiation. The dumbbell structures minimize longer wavelength shifts and improve emission efficiency of the luminescent π‐conjugated linker units in their solid states compared with the model compounds. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012. 相似文献
109.
Masahiro Yamashita Daisuke Kawakami Satoshi Matsunaga Yoshio Nakayama Mari Sasaki Shinya Takaishi Fumiyasu Iwahori Hitoshi Miyasaka Ken‐ichi Sugiura Yoshiki Wada Hiroshi Miyamae Hiroyuki Matsuzaki Hiroshi Okamoto Hisaaki Tanaka Kazuhiro Marumoto Shin‐ichi Kuroda 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2004,116(36):4867-4871
110.
Inside Cover: Enhancement of Light Absorption Ability of Synthetic Chlorophyll Derivatives by Conjugation with a Difluoroboron Diketonate Group (Chem. Eur. J. 29/2016)
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