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T. Gomi Y. Hirose T. Kurosu T. Shiraishi M. Iida Y. Gekka A. Kunioka 《Journal of Non》1980,41(1):37-46
The electrical and optical properties of the chalcogenide semiconductor (Se32Te32As4Ge32)100?xNixitx have been studied. As the Ni concentration is increased the electrical dc conductivity is drastically increased and variable range hopping conduction becomes dominant even above room temperature. The optical energy gap decreases with the Ni concentration from 1.18–0.95 eV. Ni-atoms in the chalcogenide semiconductor donate free electrons which occupy the gap state. This occupation causes the shift of the Fermi level toward the conduction band. It is an effect of this shift that the thermal activation energy is decreased. The decrease in optical energy gap is independent of the shift of the Fermi level and is ascribable to the appearance of the additional level located at 0.95 eV above the top of the valence band. This level originates from the 3d-level of the Ni-atom. 相似文献
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Chiral recognition of alkyl beta-D-pyranoside micelles toward [7] and [5] heterohelicenes possessing helical structures was investigated by 1H-NMR and CD (circular dichroism) spectroscopy. In dodecyl maltopyranoside micellar solution, P and M enantiomers of tetrathia[7]heterohelicene (7TH), which have rigid and stable helixes, manifested different chemical shifts in their 1H-NMR spectra due to differences in the diastereomeric interactions, implying that the micelles undergo stronger recognition toward the M enantiomer than the P enantiomer. On the other hand, in octyl glucopyranoside micellar solution, trithia[5]heterohelicene (5TH) and two kinds of its derivatives which are rapidly equilibrated between the enantiomers in solution, gave no distinctly resolved 1H-NMR peaks for either enantiomer even at a lowered temperature. However, these racemic [5]heterohelicenes in the micelles did develop induced CD absorptions owing to a displacement of the equilibrium, suggesting from the signs of their Cotton effects that the micelles prefer the M enantiomer to its antipode in conformity with the 1H-NMR results of 7TH. 相似文献
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Kiyonori Gomi 《Communications in Mathematical Physics》2010,294(3):863-889
We provide a finite-dimensional model of the twisted K-group twisted by any degree three integral cohomology class of a CW complex. One key to the model is Furuta’s generalized
vector bundle, and the other is a finite-dimensional approximation of Fredholm operators. 相似文献
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Reconstitution of Biosynthetic Machinery for the Synthesis of the Highly Elaborated Indole Diterpene Penitrem
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Dr. Chengwei Liu Koichi Tagami Dr. Atsushi Minami Tomoyuki Matsumoto Jens Christian Frisvad Hideyuki Suzuki Jun Ishikawa Katsuya Gomi Prof. Dr. Hideaki Oikawa 《Angewandte Chemie (International ed. in English)》2015,54(19):5748-5752
Penitrem A is one of the most elaborated members of the fungal indole diterpenes. Two separate penitrem gene clusters were identified using genomic and RNA sequencing data, and 13 out of 17 transformations in the penitrem biosynthesis were elucidated by heterologous reconstitution of the relevant genes. These reactions involve 1) a prenylation‐initiated cationic cyclization to install the bicyclo[3.2.0]heptane skeleton (PtmE), 2) a two‐step P450‐catalyzed oxidative processes forming the unique tricyclic penitrem skeleton (PtmK and PtmU), and 3) five sequential oxidative transformations (PtmKULNJ). Importantly, without conventional gene disruption, reconstitution of the biosynthetic machinery provided sufficient data to determine the pathway. It was thus demonstrated that the Aspergillus oryzae reconstitution system is a powerful method for studying the biosynthesis of complex natural products. 相似文献
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Cover Picture: Reconstitution of Biosynthetic Machinery for the Synthesis of the Highly Elaborated Indole Diterpene Penitrem (Angew. Chem. Int. Ed. 19/2015)
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Y. Kondo T. Nakamura Y. Satou T. Matsumoto N. Aoi N. Endo N. Fukuda T. Gomi Y. Hashimoto M. Ishihara S. Kawai M. Kitayama T. Kobayashi Y. Matsuda N. Matsui T. Motobayashi T. Nakabayashi T. Okumura H.J. Ong T.K. Onishi K. Ogata H. Otsu H. Sakurai S. Shimoura M. Shinohara T. Sugimoto S. Takeuchi M. Tamaki Y. Togano Y. Yanagisawa 《Physics letters. [Part B]》2010