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YOSHIHISA FUJIWARA JUN HAMADA TAKESHI AOKI TAKASHI SHIMIZU YOSHIFUMI TANIMOTO HIROAKI YONEMURA 《Molecular physics》2013,111(9):1405-1411
High magnetic field dependence of lifetimes of methylene-chain-linked radical ion pairs (RIPs) generated by photo-induced electron transfer from zinc(II) porphyrin to viologen has been confirmed in aqueous acetonitrile using a pulse magnet-laser flash photolysis apparatus. In the case of a short methylene chain it was first revealed that the dependence was definitely different from that for a long one, and was characterized by a reversal in the dependence. In addition to a long lifetime independent of the magnetic field, RIP in fields above 7T exhibited short lifetimes that depended on the field. These results were interpreted not only by spin-lattice (longitudinal) relaxation but also by spin-spin (transverse) relaxation in RIPs. 相似文献
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Carbon nanotubes were placed in magnetic fields of 80.0 kOe at temperatures of 231 K and 314 K. Scanning electron microscopy showed that nanotubes were oriented with the tube axis parallel to the fields. It was also observed that the probability of the orientation became higher, when the temperature was raised from 231 K to 314 K. The anisotropy in the susceptibilities parallel X∥ and perpendicular X ⊥ to the tube axis is suggested to increase with rise in temperature: X∥ ? X⊥ = (4 ± 2) × 10?6 emu mol?1 (per mol of carbon atoms) at 231 K and X∥ ? X⊥ = (45 ± 27) × 10?6 emu mol?1 at 314 K. 相似文献
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AWATA HIDETOSHI KUBO HARUNOBU MORITA YOSHIFUMI ODAKE SATORU SHIRAISHI JUN'ICHI 《Letters in Mathematical Physics》1997,41(1):65-78
Primary fields of the q-deformed Virasoro algebra are constructed. Commutation relations among the primary fields are studied. Adjoint actions of the deformed Virasoro current on the primary fields are represented by the shift operator f(x) = f(x). Four point functions of the primary fields enjoy the connection formula associated with the Boltzmann weights of the fusion Andrews–Baxter–Forrester model. 相似文献
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YOSHINORI TAKASHIMA KAZUYA SAKAMOTO YOSHIFUMI OIZUMI HIROYASU YAMAGUCHI SHIGEHIRO KAMITORI AKIRA HARADA 《Journal of inclusion phenomena and macrocyclic chemistry》2006,56(1-2):45-53
Cyclodextrins (α-CD, β-CD and 2,6-di-O-dimethyl-β-CD (DM-β-CD)) were found to form inclusion compounds with thiophenes (thiophene (T), bithiophene (2T)) in water and in crystalline states. The structures of α-CD–T, β-CD–2T, and DM-β-CD–2T inclusion complexes were determined by X-ray crystallography. DM-β-CD forms a 1:1 cage type complex with 2T. In contrast, β-CD formed 2:3 (CD:guest) complexes with thiophene and α-CD formed 2:3 complexes, both of the channel type. These inclusion complexes were found to polymerize by FeCl3 in the inclusion compounds in water. The products were formed poly-pseudo-rotaxane between cyclodextrins and poly(thiophene) characterized by IR, 1H-NMR and 13C CP/MAS NMR. The molecular weights of the poly-pseudo-rotaxanes with poly(thiophene) were determined by the MALDI-TOF mass spectra to be 3000–5000. In comparison between poly-pseudo-rotaxane (DM-β-CD–poly(thiophene)), authentic poly(thiophene) and the washed DM-β-CD–poly(thiophene) which was washed with DMF to dethread DM-β-CD, these poly-pseudo-rotaxane was characterized by Raman, UV–vis and fluorescence spectra. The maximum emission band of DM-β-CD–poly(thiophene) shifted to a shorter wavelength. The hypsochromic shift was derived from poly-pseudo-rotaxane with DM-β-CD. 相似文献
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