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71.
Mereacre V Nakano M Gómez-Segura J Imaz I Sporer C Wurst K Veciana J Turta C Ruiz-Molina D Jaitner P 《Inorganic chemistry》2006,45(26):10443-10445
The new hexaferrocene complex 1 has been synthesized and characterized by X-ray diffraction. Its magnetization data were fitted to a detailed theoretical model that considers nonequivalent exchange parameters between Fe ions to yield the magnetic exchange coupling values of J1/kB = -31.5 K and J2/kB = -25.8 K. Moreover, the cyclic voltammogram of complex 1 confirmed its redox activity associated with the presence of ferrocene units, with very small or negligible electronic interactions between them. 相似文献
72.
[reaction: see text] Bridged phenylthienylethenes and dithienylethenes were synthesized via Pd-catalyzed double-cyclization reactions of (Z,Z)-1,6-diaryl-1,5-hexadien-3-ynes. Pd-catalyzed as well as photoinduced Z/E isomerization of the products were also investigated. 相似文献
73.
74.
We successfully fabricated thin films of organic–inorganic layered perovskite-type compound (AEHBA)2PbCl4, where AEHBA stands for N-(2-aminoethyl)-2-hydroxybenzamide, a blue fluorescent dye that shows excited state intramolecular proton transfer (ESIPT) reaction. The formation of its highly ordered structure was readily achieved by the spin-coating of N,N-dimethylformamide solution dissolving PbCl2 and the AEHBA hydrogen chloride salt. X-ray diffraction analysis of the films revealed that organic AEHBA and inorganic PbCl4 perovskite layers were alternately stacked parallel to the substrate. In the absorption spectrum, exciton formation within the perovskite layers was confirmed by the appearance of a characteristic sharp band, while the photoluminescence spectrum showed a large Stokes-shifted band of AEHBA, indicating that it underwent an ESIPT. 相似文献
75.
Sawada M Takai Y Yamada H Yoshikawa M Arakawa R Tabuchi H Takada M Tanaka J Shizuma M Hirose K Fukuda K Tobe Y 《European journal of mass spectrometry (Chichester, England)》2004,10(1):27-37
Chiral recognition in the host-guest complexation systems of chiral crown ether hosts and amino ester guests was thoroughly examined using the electrospray ionization (ESI) mass spectrometry/enantiomer labeled (EL)-guest method. In this method, the mass spectra of a mixture of three components in a solution, a chiral host (H), an equal amount of an (S)-enantiomer guest labeled with deuterium atoms (G(S-dn)(+)) and an unlabeled (R)-enantiomer guest (G(R)+), were measured and the relative peak intensity value [I(H + G(R))(+) / I(H + G(S-dn))(+) = IRIS] of the host-guest complex ions, observed with an excess guest concentration, was taken to provide the chiral recognition ability of the host. In our earlier report (1996), we demonstrated that the apparent chiral recognition abilities using a mass spectrometer with a homemade ESI interface were depressed by about one tenth compared with the corresponding abilities obtained by fast-atom bombardment (FAB) MS. In the present study, the enantioselective complexation behaviors of various combinations of chiral crown hosts with chiral guests were further investigated in detail mainly using a modern commercial ESI/ion trap (IT) mass spectrometer. Consequently, it was found that the apparent IRIS values from the ESI-MS/EL-guest method changed significantly, depending upon the instrument used, and in particular, upon the ESI interfaces. Moreover, under the specific measuring conditions in ESI-IT-MS, the degrees of depression of the apparent chiral recognition abilities are roughly grouped into three classes, depending upon the number (or probably the type) of the hydrophobic substituents of the hosts. Representing the degrees by the slopes when plotting the apparent IRIS values in ESI-MS versus those in FAB-MS, the slopes for the three classes are (1) 1.0, (2) 0.7 and (3) 0.3; the higher the hydrophobicity of the hosts (and then, the host-guest complex ions), the lower the slope (the apparent enantioselectivity). Strengthening the degree of depression may be caused by an increase in the local concentration of the host close to the surface of the droplets produced during the electrospary ionization process. The chiral recognition ability (K(R )/ K(S)) in an equilibrated solution agrees quite well with the IRIS value in FAB-MS rather than that in ESI-MS. 相似文献
76.
Kenji Kamada Dr. Liudmil Antonov Prof. Satoru Yamada Dr. Koji Ohta Dr. Takashi Yoshimura Kazukuni Tahara Prof. Akiko Inaba Motohiro Sonoda Prof. Yoshito Tobe Prof. 《Chemphyschem》2007,8(18):2671-2677
Two‐photon absorption (TPA) properties of two trefoil‐shaped compounds with different edge linkages—tris(hexadehydrotribenzo[12]annulene) and tris(tetradehydrotribenzo[12]annulene)—and three asterisk‐shaped compounds having no edge‐linkage—hexakis(phenylethynyl)benzenes—are investigated experimentally by the open‐aperture Z‐scan and TPA‐induced fluorescence methods with wavelength tuneable femtosecond pulses. The compound with ethynylene edge‐linkage exhibits the most intense TPA (the maximal TPA cross section is 1300±170 GM at 572 nm where 1 GM=10?50 cm4 s molecule?1 photon?1). The TPA activity of the compounds is primarily explained in terms of the planarity of the molecules in relation with the type of edge‐linkage. 相似文献
77.
Kazutaka Kamitani Motohiro Uo Hiroyuki Inoue Akio Makishima 《Journal of Sol-Gel Science and Technology》1993,1(1):85-92
Tetraphenylporphinetetrasulfonic acid (TPPS), which is well known as a photochemical hole-burning (PHB) dye, was incorporated in silica gels obtained by the sol-gel process from tetramethoxysilane (TMOS). The form of TPPS must be free base (H2P), which exists in basic condition, to be active in PHB. To obtain transparent and higher density silica gels doped with free-base TPPS, two-step hydrolysis processes using solutions containing NaOH were developed, and the gels having bulk density of about 1.5 g/cm3 were synthesized. The form of TPPS in the gels was investigated by measuring the absorption and luminescence spectra, and it was found that in the silica gels almost all the TPPS retained free-base form at the molar ratio of NaOH/TMOS above 10–3. 相似文献
78.
Kakehashi R Shizuma M Yamamura S Takeda T 《Journal of colloid and interface science》2004,279(1):253-258
We have investigated the mixing behavior of binary mixtures of the alkylglucosides (CnG) octyl beta-D-glucoside and decyl D-glucoside in combination with sodium oleate (NaOl), and the amine oxide surfactants (AO) N,N-dimethyldodecylamine oxide, N,N-bis (2-hydroxyethyl)dodecylamine oxide, and 3-lauramidopropyl-N,N-dimethylamine oxide in combination with NaOl. From the equilibrium surface tension measurements, the critical micelle concentration (cmc) data were obtained as functions of the composition. Values of the cmc were analyzed according to both the regular solution model developed by Rubingh for mixed micelles and Maeda's formulation for ionic/nonionic mixed micelles. Two interaction parameters, beta and B1, were estimated from the regular solution model and Maeda's formulation, respectively. For NaOl/CnG mixed systems, a decrease in the hydrocarbon chain length of CnG resulted in a stronger interaction with NaOl from both beta and B1 values. For NaOl/AO mixed systems, the bulkiness of a polar head group of AO surfactants influenced the interaction between NaOl and AO. The dynamic surface tension measurements show that all surface tension values of surfactant solutions examined decreased with the time. We found that the time dependence of surface tension values for NaOl mixed systems was greatly influenced by the presence of NaOl rather than the other component. 相似文献
79.
Jun-ichi Kadokawa Mitsuru Sato Masa Karasu Hideyuki Tagaya Koji Chiba 《Angewandte Chemie (International ed. in English)》1998,37(17):2373-2376
Sugar dihydroozaxole monomers with two free hydroxyl groups undergo acid-catalyzed polymerization to hyperbranched aminopolysaccharides [Eq. (a)]. Their molecular weights were determined by the light-scattering method to be between 2.3×105 and 7.6×105. The degree of branching determined by 1H NMR spectroscopy after reaction with [iPr2Si(Cl)]2O is close to the ideal value. Ts=MeC6H4SO2, CSA=10-camphorsulfonic acid. 相似文献
80.