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101.
Uemura T Kitagawa K Horike S Kawamura T Kitagawa S Mizuno M Endo K 《Chemical communications (Cambridge, England)》2005,(48):5968-5970
The first radical polymerisation of styrene in porous coordination polymers has been carried out, providing stable propagating radicals (living radicals), and a specific space effect of the host frameworks on the monomer reactivity is demonstrated. 相似文献
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103.
We give a new proof of Bartholdi's theorem for the Bartholdi zeta function of a graph.
Supported by Grant-in-Aid for Science Research (C) 相似文献
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We investigated femtosecond and picosecond time-resolved fluorescence dynamics of a tetrameric fluorescent protein Kaede with a red chromophore (red Kaede) to examine a relationship between the excited-state dynamics and a quaternary structure of the fluorescent protein. Red Kaede was obtained by photoconversion from green Kaede that was cloned from a stony coral Trachyphyllia geoffroyi. In common with other typical fluorescent proteins, a chromophore of red Kaede has two protonation states, the neutral and the anionic forms in equilibrium. Time-resolved fluorescence measurements clarified that excitation of the neutral form gives the anionic excited state with a time constant of 13 ps at pH 7.5. This conversion process was attributed to fluorescence resonance energy transfer (FRET) from the photoexcited neutral form to the ground-state anionic form that is located in an adjacent subunit in the tetramer. The time-resolved fluorescence data measured at different pH revealed that excited-state proton transfer (ESPT) also occurs with a time constant of 300 ps and hence that the FRET and ESPT take place simultaneously in the fluorescent protein as competing processes. The ESPT rate in red Kaede was significantly slower than the rate in Aequorea GFP, which highly likely arises from the different hydrogen bond network around the chromophore. 相似文献
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109.
Hisashi Yoshida Akinori Okamoto Seigi Mizuno Hiroshi Tochihara 《Surface science》2010,604(5-6):535-540
Low-energy electron diffraction (LEED) have been used to determine the Cu(0 0 1)–c(4 × 4)-Sn structure formed at 300 K. It is demonstrated that a structural model suggested by scanning tunneling microscopy observations is correct: The model consists of one substitutional Sn atom and four Sn adatoms in the unit cell. Optimum parameters of the determined c(4 × 4) structure reveal that Sn adatoms laterally are displaced by 0.30 Å away from ideal fourfold-hollow sites along the 〈100〉 directions. It is proposed that such displacements of the Sn adatoms cause the formation of a network of octagonal rings on Cu(0 0 1). The substitutional Sn atom is located at each center of the octagonal rings. The formation conditions of the network are discussed. 相似文献
110.
Hirobumi Mizuno 《Discrete Mathematics》2006,306(2):220-230
We give a decomposition formula for the Bartholdi zeta function of a graph G which is partitioned into some irregular coverings. As a corollary, we obtain a decomposition formula for the Bartholdi zeta function of G which is partitioned into some regular coverings. 相似文献