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41.
A TiO2(1 1 0)-(1 × 1) surface was prepared in an ultra-high vacuum, transported in laboratory air, and observed with a scanning tunneling microscope (STM) operated in a vacuum of 10−4 Pa. Empty state images showed atomically flat terraces separated by single-height steps, on which 5-fold-coordinated surface Ti atoms were observed as spots arranged in a rectangular lattice. The Ru(4,4′-dicarboxy-2,2′-bipyridine)2(NCS)2 (N3) dye was adsorbed on the TiO2 surface by immersing the TiO2 wafer into an acetonitrile solution of the dye. In the empty state images, individual N3 molecules were observed as oval particles protruding by 0.6 nm from the TiO2 surface. The oval shape elongated to the [1 0] directions was attributed to electron tunneling from tip to unoccupied states localized at the two carboxyl groups bound to the TiO2 surface. 相似文献
42.
Toshihiko Hoshi Ken-ichi Kumagai Keita Inoue Shigendo Enomoto Yoko Nobe Michio Kobayashi 《Journal of luminescence》2008,128(8):1353-1358
Tris(8-quinolinolato)aluminum(III) (Alq3) shows electronic absorption bands at 378, 360 (in a 1:1 mixed solvent of methanol and ethanol (ME) at 77 K), 334, 316, 300, 263, 255.8, and 233 nm in ethanol at room temperature. According to the polarized fluorescence excitation spectrum together with MO calculations, for instance, the 360 nm band is assigned to an LL CT transition (an intramolecular charge transfer transition between two ligands), and the 378 nm band to an LM/ML CT one (an intramolecular charge transfer transition between ligand and metal). Alq3 shows a broad fluorescence band peaking at around 478 nm in the ME matrix at 77 K. The emission spectrum measured with a phosphoroscope has two emission bands at 567 and 478 nm. The 567 nm band accompanies vibronic bands at 578 and 605 nm, being safely assigned to a phosphorescence of Alq3. The lifetimes of the 478 and 567 nm bands are both 5.4 ms. The lifetime of the 478 nm band together with the band position and its band shape indicate that this band can be assigned to a delayed fluorescence. 相似文献
43.
Kenta Nagamine Keita Hirose Tsuyoshi Honma Takayuki Komatsu 《Solid State Ionics》2008,179(13-14):508-515
The glasses with the composition of 37.5Li2O–(25 − x)Fe2O3–xNb2O5–37.5P2O5 (mol%) (x = 5,10,15) are prepared, and it is found that the addition of Nb2O5 is effective for the glass formation in the lithium iron phosphate system. The glass–ceramics consisting of Nasicon-type Li3Fe2(PO4)3 crystals with an orthorhombic structure are developed through conventional crystallization in an electric furnace, showing electrical conductivities of 3 × 10− 6 Scm− 1 at room temperature and the activation energies of 0.48 eV (x = 5) and 0.51 eV (x = 10) for Li+ ion conduction in the temperature range of 30–200 °C. A continuous wave Nd:YAG laser (wavelength: 1064 nm) with powers of 0.14–0.30 W and a scanning speed of 10 μm/s is irradiated onto the surface of the glasses, and the formation of Li3Fe2(PO4)3 crystals is confirmed from XRD analyses and micro-Raman scattering spectra. The crystallization of the precursor glasses is considered as new route for the fabrication of Li3Fe2(PO4)3 crystals being candidates for use as electrolyte materials in lithium ion secondary batteries. 相似文献
44.
Dr. Chihiro Maeda Keita Suka Keiji Nagahata Dr. Kazuto Takaishi Prof. Tadashi Ema 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(19):4261-4268
A series of carbazole-based boron dipyrromethenes (BODIPYs) 2 a – g bearing binaphthyl units have been synthesized by the Et2AlCl-mediated reaction of the corresponding BODIPY difluorides 1 a – g with 1,1′-binaphthalene-2,2′-diol. Substituents such as halogen, nitrile, and amino groups were tolerated under the reaction conditions, and the reaction of the phenylethynyl-substituted 1 h gave (R,R)- 3 h bearing two binaphthyl units. The chiroptical properties of these dyes with different substituents were investigated by UV/Vis, CD, fluorescence, and circularly polarized luminescence (CPL) spectroscopy. The CD spectra showed Cotton effects in the absorption region of the BODIPY moieties. In addition, they showed CPL both in solution and in the solid state. Interestingly, several dyes recorded higher glum values in the solid state, probably due to intermolecular interactions. Because (R,R)- 3 h recorded relatively low glum values, the diastereomer (R,S)- 3 h was prepared. The (R,S) diastereomer showed intense CPL, which suggests a synergetic effect of the two binaphthyl groups. Finally, chiral carbazole-based BODIPY dimers have been synthesized for the first time and their chiroptical properties were investigated. They showed redshifted fluorescence and CPL, which reached the near-IR (NIR) region in the solid state. 相似文献
45.
Ferroelectric Coordination Polymers Self‐Assembled from Mesogenic Zinc(II) Porphyrin and Dipolar Bridging Ligands 下载免费PDF全文
Dr. Joseph K.‐H. Hui Hiroyuki Kishida Keita Ishiba Kenta Takemasu Dr. Masa‐aki Morikawa Prof. Dr. Nobuo Kimizuka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(40):14213-14218
A new class of ferroelectric coordination‐based polymers has been developed by the self‐assembly of lipophilic zinc porphyrin ( ZnP ) and ditopic bridging ligands. The ligands contain dipolar benzothiadiazole or fluorobenzene units, which are axially coordinated to ZnP with the dipole moments oriented perpendicular to the coordination axes. The coordination‐based polymers show ferroelectric characteristics in the liquid crystalline state, as revealed by distinctive hysteresis in the polarization–electric field (P–E) loops and inversion current peaks in current–voltage (I–V) loops. The observed ferroelectric properties are explainable by flip–flop rotation of the dipolar axle ligands induced by the applied electric field, as demonstrated by the positive‐up–negative‐down (PUND) measurements. The present system provides a new operating principle in supramolecular ferroelectrics. 相似文献
46.
Transport in Porous Media - We study the impact, on the drying rate, of the presence of suspended elements, such as calcium sulfate ions, in the interstitial fluid of a porous medium. In order to... 相似文献
47.
Facile Fabrication of Concentrated Polymer Brushes with Complex Patterning by Photocontrolled Organocatalyzed Living Radical Polymerization 下载免费PDF全文
Dr. Chen‐Gang Wang Chen Chen Dr. Keita Sakakibara Prof. Dr. Yoshinobu Tsujii Prof. Dr. Atsushi Goto 《Angewandte Chemie (International ed. in English)》2018,57(41):13504-13508
Photocontrolled surface‐initiated reversible complexation mediated polymerization (photo‐SI‐RCMP) was successfully applied to fabricate concentrated polymer brushes with complex patterning structures. Positive‐type patterned polymer brushes were obtained by photo‐SI‐RCMP under visible light (550(±50) nm) using photomasks. A particularly interesting finding was that negative‐type patterned polymer brushes were also obtainable in a facile manner. A nonspecial UV light (250–385 nm) enabled the preparation of pre‐patterned initiator surfaces in a remarkably short time (1 min), leading to negative‐type patterned polymer brushes. Based on this unique selectivity between visible and UV light, the combination of two patterning techniques enabled the preparation of complex patterned brushes, including diblock copolymers, binary polymers, and functional binary polymers, without multistep immobilization of one or more initiators on the surfaces. 相似文献
48.
Borderline metal complexes, especially Bi(OTf)3, efficiently catalyze the carbo-oxycarbonylation of alkynyl esters to form multisubstituted lactones in moderate to high yields. 相似文献
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