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81.
82.
Inside Back Cover: Plasmon‐Assisted Water Splitting Using Two Sides of the Same SrTiO3 Single‐Crystal Substrate: Conversion of Visible Light to Chemical Energy (Angew. Chem. Int. Ed. 39/2014) 下载免费PDF全文
83.
Haruko Ikeuchi Kaoru Naganuma Marie Ichikawa Hiromichi Ozawa Tomoya Ino Makoto Sato Hiroko Yonezawa Sonomi Mukaida Akihiro Yamamoto Takeshi Hashimoto 《Journal of solution chemistry》2007,36(10):1243-1259
The diffusion coefficients of several tris(β-diketonato) ruthenium complexes in acetonitrile solutions containing a supporting electrolyte were determined by chronoamperometry.
The diffusion coefficients of the charged complexes, which were produced by electrochemical oxidation or reduction, were also
determined by double potential step chronoamperometry. Two kinds of radii of the complexes were evaluated. One was the Van
der Waals radius and the other was the geometric distance from the center of the complex to the outer surface of the farthest
atom. The latter quantity was determined from X-ray diffractometric data. The diffusion coefficients of the neutral complexes
were discussed on the basis of the Stokes-Einstein equation. Those of charged complexes could not be explained by the theoretical
equation presented by Hubbard and Onsager. 相似文献
84.
85.
We construct extremal singly even self-dual [64,32,12] codes with weight enumerators which were not known to be attainable. In particular, we find some codes whose shadows have minimum weight 12. By considering their doubly even neighbors, extremal doubly even self-dual [64,32,12] codes with covering radius 12 are constructed for the first time. 相似文献
86.
Masaki Takahashi Tomoya OdagiHiroko Tomita Tatsuo OshikawaMitsuji Yamashita 《Tetrahedron letters》2003,44(12):2455-2458
A new type of polyaromatic dendrimer composed of six anthracene groups was synthesized, which showed a monomeric fluorescence feature with a diminished quantum yield due to intramolecular self-quenching processes in the dendritic framework. 相似文献
87.
Kiyoshi Tanaka Tomoya Okada Fumio Yoneda Tomohisa Nagamatsu Kazunori Kuroda 《Tetrahedron letters》1984,25(16):1741-1742
1,5-Dihydro-5-deazaflavin derivatives possessing a chiral substituent at N(3) position were synthesized, with which moderate asymmetric induction was observed in the reduction of ethyl benzoylformate. 相似文献
88.
Case studies of the Baeyer-Villiger reaction applied to diand trifluoromethylketone derivatives and the effect of the fluoromethyl groups on the Baeyer-Villiger reaction, are described. 相似文献
89.
Zhao Y Higashihara T Sugiyama K Hirao A 《Journal of the American Chemical Society》2005,127(41):14158-14159
Novel 3-arm ABC, 4-arm ABCD, and 5-arm ABCDE asymmetric star polymers comprising the conductive polyacetylene precursor, poly(4-methylphenyl vinyl sulfoxide) (PMePVSO), and other segments, such as polystyrene, poly(alpha-methylstyrene), poly(4-methoxystyrene), poly(4-trimethylsilylstyrene), and poly(4-methylstyrene), were synthesized by the methodology based on living anionic polymerization using DPE-functionalized polymers. This methodology involves the addition reaction of a DPE-functionalized polymer to a living anionic polymer followed by the living anionic polymerization of MePVSO initiated from the in situ formed polymer anion with two, three, or four polymer segments. The resultant asymmetric star polymers possessed predetermined molecular weights, narrow molecular weight distributions (Mw/Mn < 1.03), and desired compositions as confirmed by SEC, 1H NMR, SLS, and elemental analysis. After thermal treatment, the PMePVSO segment in the star polymer could be completely converted into a conductive polyacetylene segment, evident from TGA and elemental analysis. These asymmetric star polymers are expected to exhibit interesting solution properties and unique microphase-separated morphological suprastructures with potential applications in nanoscopic conductive materials. Moreover, this methodology can afford the target asymmetric star polymers with arm segments varying in a wide range and enables the synthesis of more complex macromolecular architectures. 相似文献
90.
Tomoya Ito Koji Suda Takuya Kumamoto Waka Nakanishi Toshiko Watanabe Tsutomu Ishikawa Hiroko Seki Masatoshi Kawahata Kentaro Yamaguchi Yasumitsu Ogura Kazuo T. Suzuki 《Molecular diversity》2010,14(1):131-145
The role of o-bisguanidinobenzenes (BGBs) as new Brønsted base ligands for arsenic and phosphoric acids was examined. In solution state, complexation was evaluated by Job’s plot in 1H NMR experiment, indicating a 1:1 complex formation, whereas in solid state crystalline structures of complexes obtained were addressed by X-ray crystallographic analysis and/or solid state 13C NMR experiment, in which 1:2 complexes between the BGB and the acid components were normally formed. Based on these results, Merrifield and Hypogel® resin-anchored BGBs were designed and prepared as the corresponding polymer-supported host ligands. Evaluation of their coordination ability with metal salts (ZnCl2 and CoCl2) and arsenic acid in aqueous media by ICP-MS showed that the latter Hypogel® resin-anchored BGBs acted as effective immobilized base ligands. 相似文献