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991.
Sato S Nakamura T Nitobe S Kiba T Hosokawa K Kasajima T Otsuka I Akimoto S Kakuchi T 《The journal of physical chemistry. B》2006,110(43):21444-21449
Dimethylanthracene (DMA), which exhibits almost no self-association in bulk organic solvents, forms a dimer and emits excimer-like fluorescence in a gamma-cyclodextrin nanocavity in a dilute aqueous solution. The 1Bb and 1La electronic transitions of the DMA dimer split by 2230 and 344 cm(-1), respectively, in a fluorescence excitation spectrum obtained with the excimer-like emission. From these energy splits, the structure of dimer in relation to a dielectric constant inside gamma-CD was discussed on the basis of atom-atom Lennard-Jones potential calculations including Coulombic interactions. Excitation relaxations of DMA in the presence of alpha-, beta-, and gamma-CDs in aqueous solutions were investigated by time-resolved fluorescence. The results suggest that both the hydrated and anhydrated species exist in the alpha- and gamma-CD complexes, while only the anhydrated species exists in the beta-CD complex. 相似文献
992.
Sahoo AK Nakamura Y Aratani N Kim KS Noh SB Shinokubo H Kim D Osuka A 《Organic letters》2006,8(18):4141-4144
Highly efficient synthesis of meso,meso-dibromo doubly and triply fused diporphyrins has been achieved through a powerful oxidative coupling mediated by AuCl3-AgOTf combination. In addition, palladium-catalyzed debromination of meso-bromoporphyrins has been developed. This debromination protocol enables employment of bromine as a protecting group for the reactive meso-position of porphyrins. 相似文献
993.
[reaction: see text] A series of modified gamma-cyclodextrins (CDs) with a flexible or rigid cap, synthesized and used as chiral supramolecular hosts for mediating the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid, significantly improved the chemical and optical yields of chiral head-to-head cyclodimer 3, while the gamma-CD with a rigid cap dramatically inverted the stereochemical outcomes and further improved the enantioselectivities of both head-to-tail and head-to-head dimers 2 and 3. 相似文献
994.
[reaction: see text] Spirocyclic C-arylribosides were synthesized from the known gamma-ribonolactone derivative. Lithium acetylide addition followed by glycosylation with 3-(trimethylsilyl)propargyl alcohol converted the ribonolactone to silylated diynes. After desilylation or iodination, subsequent ruthenium-catalyzed cycloaddition of resultant diynes with alkynes or chloroacetonitrile gave spirocyclic C-arylribosides. 相似文献
995.
[reaction: see text] A boat-type of chelated bicyclic transition state involving highly diastereoselective construction of three contiguous stereogenic centers in the Reformatsky reaction of indium enolates with alpha-alkoxy/hydroxy ketones is proposed. alpha-Hydroxy ketones with indium enolates furnished highly diastereoselective lactones, while alpha-alkoxy ketones gave acyclic esters in moderate selectivities. X-ray structure analyses of key products unequivocally revealed the unexpected stereochemistry of products and the reaction pathway. 相似文献
996.
The article gives constructions of disjoint 5‐designs obtained from permutation groups and extremal self‐dual codes. Several new simple 5‐designs are found with parameters that were left open in the table of 5‐designs given in (G. B. Khosrovshahi and R. Laue, t‐Designs with t⩾3, in “Handbook of Combinatorial Designs”, 2nd edn, C. J. Colbourn and J. H. Dinitz (Editors), Chapman & Hall/CRC, Boca Raton, FL, 2007, pp. 79–101), namely, 5−(v, k, λ) designs with (v, k, λ)=(18, 8, 2m) (m=6, 9), (19, 9, 7m) (m=6, 9), (24, 9, 6m) (m=3, 4, 5), (25, 9, 30), (25, 10, 24m) (m=4, 5), (26, 10, 126), (30, 12, 440), (32, 6, 3m) (m=2, 3, 4), (33, 7, 84), and (36, 12, 45n) for 2⩽n⩽17. These results imply that a simple 5−(v, k, λ) design with (v, k)=(24, 9), (25, 9), (26, 10), (32, 6), or (33, 7) exists for all admissible values of λ. © 2010 Wiley Periodicals, Inc. J Combin Designs 18: 305–317, 2010 相似文献
997.
Takashi Nakamura 《The Ramanujan Journal》2010,21(3):285-302
In this paper, we consider multiplication formulas and their inversion formulas for Hurwitz–Lerch zeta functions. Inversion
formulas give simple proofs of known results, and also show generalizations of those results. Next, we give a generalization
of digamma and gamma functions in terms of Hurwitz–Lerch zeta functions, and consider its properties. In all the sections,
various results are always proved by multiplication and inversion formulas. 相似文献
998.
Nithima Khaorapapong Kazuyuki Kuroda Hideo Hashizume Makoto Ogawa 《Molecular Crystals and Liquid Crystals》2013,570(2):351-356
Abstract Intercalation of 4,4′-bipyridine into the interlayer spaces of cobalt(II), nickel(II) and copper(II)-montmorillonites by solid-solid reactions was investigated. The successful intercalation of 4,4′-bipyridine and the complex formation in the interlayer spaces of montmorillonites was confirmed by powder XRD (the change in the basal spacings) as well as IR and the thermal analysis of the products. 相似文献
999.
Abstract We study ground state phase diagrams for the MMX chains, using a one-dimensional dimerized 3/4-filled extended Hubbard-Peierls model with site diagonal and off-diagonal electron-lattice interactions. The ground states are obtained mainly in the Hartree-Fock approximation, and their accuracy is checked by the exact diagonalization of small clusters. We find a new phase in addition to frequently considered phases and compare our results with experimental results. 相似文献
1000.
Abstract This paper describes the changes in biochemical activities of sarcoplasmic reticulum(SR) and Ca2+ release from SR in the rabbit skeletal muscle subjected to a high pressure treatment(100∽300 MPa) to investigate the mechanism for pressure-induced meat tenderization and acceleration of meat conditioning. Pressure-dependent changes were observed in the both extra and basal ATPase activities of SR prepared from the muscles exposed to high pressure. Ca2+ uptaking ability of SR vesicles measured by fluorescent chelating reagent, indo-1, decreased with increasing pressure applied to the muscle. Ultrastructural studies revealed that Ca2+ which was mainly localized in the SR region of the untreated fiber bundles was translocated into myofibrils in the pressurized muscle. Obtained results in this report may be one of the causes for meat tenderization and acceleration of meat conditioning induced by high pressure treatment. 相似文献