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31.
The system Au/Si(100) has been studied using LEED and AES. Au films grow as Au(111) | Si(100) having six azimuthally rotated orientations at low deposition temperatures below 50°C after the formation of intermediate gold suicide layers. Crystalline gold silicide thin layers are formed on the Au(111) film after heat treatment at 100–400°C. Two types of suicide LEED pattern observed seem to have no correlation with crystallographic data reported on quenched alloy films. Heat treatment over 450°C leads to agglomeration of the film, producing a series of Au-induced superstructures. Heat treatment of the Au film over 1000°C regenerates the clean Si surface accompanied with many etch pits. 相似文献
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The growth process of silver on a Si(111) substrate has been studied in detail by low-energy ion-scattering spectroscopy (ISS) combined with LEED-AES. Neon ions of 500 eV were used as probe ions of ISS. The ISS experiments have revealed that the growth at room temperature and at high temperature are quite different from each other even in the submonolayer coverage range. The following growth models have been proposed for the respective temperatures. At room temperature, the deposited Ag forms a two-dimensional (2D) island at around 2/3 monolayer (ML) coverage, where the Ag atoms are packed commensurately with the Si(111)1 substrate. One third of the substrate Si surface remains uncovered there. Then it starts to develop into Ag crystal, and at a few ML coverage a 3D island of bulk Ag crystal grows directly on the substrate. An intermediate layer, which covers uniformly the whole surface before the growth of Ag crystal, does not exist. At high temperatures (>~200°C), the well-known Si(111)√3-Ag layer is formed as an intermediate layer, which consists of 2/3 ML of Ag atoms and covers the whole surface uniformly. These Ag atoms are embedded in the first double layer of the Si substrate. It is concluded that the formation of the √3 structure needs relatively high activation energy which may originate from the large displacement of Si atoms owing to the embedment of the Ag atoms, and does not proceed below about 200°C. The most stable state of the Ag atoms on the outermost Si layer is in the shape of an island, both for the Si(111) surface and for the Si(111)√3-Ag surface. 相似文献
34.
A clay-like conductive material comprising polyaniline-loaded carbon black particles and an ethyleneoxide-substituted imidazolium iodide was prepared. The material was sandwiched between dye-coated porous TiO2 and counter-electrode to form a solid-state dye-sensitized solar cell, which works with overall conversion efficiencies of 3.48% and 4.07% for AM 1.5, 100 mW cm(-2) and 23 mW cm(-2) irradiation, respectively. 相似文献
35.
Takayama H Misawa K Okada N Ishikawa H Kitajima M Hatori Y Murayama T Wongseripipatana S Tashima K Matsumoto K Horie S 《Organic letters》2006,8(25):5705-5708
Treatment of indole alkaloids with hypervalent iodine in the presence of ethylene glycol provides 2,3-ethylene glycol bridged adducts that could be converted into the original indoles under mild reductive conditions. This procedure, which involves masking of the reactivity of the indole nucleus at the beta-position, was utilized for the modification of the benzene ring of the indoline derivative and was applied to the preparation of potent opioid receptor agonists with the Corynanthe skeleton. [reaction: see text] 相似文献
36.
Naoyuki Toriumi Norihito Asano Takayuki Ikeno Atsuya Muranaka Kenjiro Hanaoka Yasuteru Urano Masanobu Uchiyama 《Angewandte Chemie (International ed. in English)》2019,58(23):7788-7791
Near‐infrared (NIR) imaging techniques have attracted significant attention for biological and medicinal applications due to the ability of NIR to penetrate deeply into tissues. However, there are very few stable, activatable molecular probes that can utilize NIR light in the wavelength range beyond 800 nm. Herein, we report a new activatable NIR system for photoacoustic imaging based on tautomeric benziphthalocyanines (BPcs). We found that the existence of a free hydroxyl group is crucial for NIR absorption of BPcs. Synthesized water‐soluble hydroxy BPcs exhibited high photostability and no fluorescence, which are desirable features for photoacoustic imaging. We synthesized BPcs in which the free hydroxyl group was masked by an esterase‐labile or an H2O2‐labile group. The photoacoustic signals of these hydroxy‐masked BPcs were increased upon NIR excitation at 880 nm in the presence of esterase or H2O2, respectively. These are rare examples of activatable probes utilizing NIR light at around 900 nm. 相似文献
37.
Atsushi Goto Tadashi Shimizu Kenjiro Hashi Shinobu Ohki 《Applied Physics A: Materials Science & Processing》2008,93(2):533-536
We present a scheme of surface-sensitive nuclear magnetic resonance in optically pumped semiconductors, where an NMR signal from a part of the surface of a bulk compound semiconductor is detected
apart from the bulk signal. It utilizes optically oriented nuclei with a long spin-lattice relaxation time as a polarization
reservoir for the second (target) nuclei to be detected. It provides a basis for the nuclear spin polarizer [IEEE Trans. Appl. Supercond. 14:1635, 2004], which is a polarization reservoir at the surface of the optically pumped semiconductor that polarizes nuclear spins in
a target material in contact through the nanostructured interfaces. 相似文献
38.
Use of 0.25 mol % of the N, N, P-tridentate ligand containing the 2-quinolyl moiety ( 1 and 2) and 0.1 mol % of Cu(OTf) 2 enabled the enantioselective 1,4-addition of dialkylzincs to cyclic enones to produce 1,4-adducts in up to 99% ee. 相似文献
39.
Tsutomu Oishi Kenjiro Onimura Yukio Isobe Hiroaki Yanagihara Hiromori Tsutsumi 《Journal of polymer science. Part A, Polymer chemistry》2000,38(2):310-320
Asymmetric anionic homopolymerizations of N‐substituted maleimide (RMI) bearing bulky substituents [R = benzyl, diphenylmethyl (DPhMI), 9‐fluorenyl (9‐FlMI), triphenylmethyl, (diphenylmethyloxycarbonyl)methyl, (9‐fluorenyloxycarbonyl)methyl] were carried out with complexes of organometal compounds (alkyllithium, diethylzinc) with six chiral ligands to obtain optically active polymers. The chiroptical properties of the polymers were affected strongly by the substituents on nitrogen in the maleimide ring, the organometal and chiral ligands. Poly(DPhMI) initiated by an n‐butyllithium/(−)‐sparteine (Sp) complex showed a positive specific rotation ([α] +60.3°). Poly(9‐FlMI) prepared with a florenyllithium/Sp complex exhibited the highest specific rotation (+65.7°). The specific rotations of the poly(RMI) obtained were attributed to different contents between the stereogenic centers (S,S) and (R,R) based on threo‐diisotactic structures of the main chain. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 310–320, 2000 相似文献
40.