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121.
Yokokita Takuya Yano Shinya Komori Yukiko Haba Hiromitsu 《Journal of Radioanalytical and Nuclear Chemistry》2022,331(2):1127-1134
Journal of Radioanalytical and Nuclear Chemistry - To investigate sulfate complex formation of Rf, we performed batch-wise ion-exchange experiments of its homologues Zr and Hf and its pseudo... 相似文献
122.
Masahito Katto Hironari Zushi Wataru Nagaya Shinya Harano Ryota Matsumoto Atushi Yokotani Masanori Kaku Shoichi Kubodera Noriaki Miyanaga 《Applied Physics A: Materials Science & Processing》2010,101(2):297-301
We have developed intense vacuum ultraviolet (VUV) radiation sources for advanced material processing, such as photochemical
surface reactions and precise processing on a nanometer scale. We have constructed a new VUV laser system to generate sub-picosecond
pulses at the wavelength of 126 nm. A seed VUV pulse was generated in Xe as the 7th harmonic of a 882-nm Ti:sapphire laser.
The optimum conversion was achieved at the pressure of 1.2 Torr. The seed pulse will be amplified by the Ar2*\mathrm{Ar}_{2}^{*} media generated by an optical-field-induced ionization Ar plasma produced by the Ti:sapphire laser. We have obtained a gain
coefficient of g=0.16 cm−1. Our developing system will provide VUV ultra-short pulses with sub-μJ energy at a repetition rate of 1 kHz. 相似文献
123.
Chemically disordered face-centered cubic (fcc) FePt nanoparticles (NPs) with a mean diameter of 9 nm were synthesized via pyrolysis of iron(III) ethoxide and platinum(II) acetylacetonate. The surface ligands of these NPs were then exchanged from oleic acid to tetramethylammonium hydroxide (TMAOH) to measure the longitudinal (T1) and transverse (T2) proton relaxation times of aqueous dispersion of FePt NPs. Magnetic resonance relaxometry reveals that TMAOH-capped FePt NPs have a higher T2-shortening effect than conventional superparamagnetic iron oxide NPs, indicating that fcc-phase FePt NPs might be superior negative contrast agents for magnetic resonance imaging. 相似文献
124.
Dr. Yasuyuki Yamada Hayato Iida Shinya Shibano Dr. Nozomi Mihara Prof. Tatsuhisa Kato Prof. Kentaro Tanaka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(37):e202200819
Spatial distance is an important factor in controlling the functional interactions between molecular units in a conjugate; therefore, the bridging unit has been closely examined. Here, we examined the effect of the flexibility of bridging alkyl chains on the proximity of stacked porphyrin and phthalocyanine conjugated with a fourfold rotaxane linkage. We found that closely stacking two π systems requires bridging alkyl chains above a certain length, and the shorter bridges hinder stacking because of their lower flexibility. The stacking distance between porphyrin and phthalocyanine in the conjugate with decyl (C10) chains was estimated to be 4.03 Å and showed a unique physical character arising from short-distance interactions. The longer alkyl chains minimized steric restriction inside the fourfold rotaxane and allowed efficient communication between the porphyrin and phthalocyanine units. This is due to the flexibility of the side chains. 相似文献
125.
Morohashi N Noji S Nakayama H Kudo Y Tanaka S Kabuto C Hattori T 《Organic letters》2011,13(13):3292-3295
Powdery crystals of p-tert-butylthiacalix[4]arene (2) selectively include EtOH from 1:1 mixtures of MeOH-EtOH and EtOH-PrOH, and EtCO(2)H from HCO(2)H-EtCO(2)H. On the other hand, no acid is included from HCO(2)H-MeCO(2)H, even though MeCO(2)H is included from the neat acid. The origins of these phenomena are discussed based on X-ray analysis of inclusion crystals prepared separately by crystallization. 相似文献
126.
Mai Kuroha Hikaru Hemmi Mayumi Ohnishi-Kameyama Shinya Kodani 《Tetrahedron letters》2017,58(35):3429-3432
A new lasso peptide named subterisin was isolated from the culture broth of Sphingomonas subterranea NBRC 16086T. The molecular formula of subterisin was established as C78H121O22N21 based on accurate mass analysis. The chemical structure of subterisin was determined by 2D NMR experiments. The presence of macrolactam ring of Gly1–Glu8 was indicated by NOESY experiment and MS/MS analysis. The three-dimensional structure of subterisin in solution was established by calculation based on NMR data. The proposed biosynthetic gene cluster of subterisin was found on the genome of S. subterranea. 相似文献
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130.
Masatoshi Hasegawa Daiki Hirano Mari Fujii Misako Haga Eiichiro Takezawa Shinya Yamaguchi Atsushi Ishikawa Takashi Kagayama 《Journal of polymer science. Part A, Polymer chemistry》2013,51(3):575-592
This work presents novel colorless polyimides (PIs) derived from 1R,2S,4S,5R‐cyclohexanetetracarboxylic dianhydride (H″‐PMDA). Isomer effects were also discussed by comparing with PI systems derived from conventional hydrogenated pyromellitic dianhydride, that is, 1S,2R,4S,5R‐cyclohexanetetracarboxylic dianhydride (H‐PMDA). H″‐PMDA was much more reactive with various diamines than H‐PMDA, and the former led to PI precursors with much higher molecular weights. The results can be explained from the quite different steric structures of these isomers. The thermally imidized H″‐PMDA‐based films were colorless regardless of diamines because of inhibited charge‐transfer interaction. In particular, the H″‐PMDA/4,4′‐oxydianiline system simultaneously achieved a very high Tg exceeding 300 °C, high toughness (elongation at break > 70%), and good solution processability. In contrast, the H‐PMDA‐based counterparts were essentially insoluble. The outstanding solubility of the former probably results from disturbed chain stacking by its nonplanar steric structure. An advantage of chemical imidization process is also proposed. In some cases, a copolymerization approach with an aromatic tetracarboxylic dianhydride was effective to improve the thermal expansion property. The results suggest that the H″‐PMDA‐based PI systems can be promising candidates for novel high‐temperature plastic substrate materials in electronic paper displays. A potential application as optical compensation film materials in liquid crystal displays (LCD) is also proposed in this work. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献