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91.
The gelation ability of 10 alkylammonium (CnH(2n+1)NH3+ where n=4-11, 12 and 16) anthracene-9-carboxylates (1n) has been evaluated. In cyclohexane, 1(4), 1(5), 1(6) and 1(7) only provided precipitates whereas 1(11), 1(12) and 1(16) provided very viscous solutions. In contrast, 1(8) 1(9) and 1(10) resulted in gels. The critical gelation concentration of 1(10) was very low (5.0 x 10(-4) mol dm(-3)). SEM observations showed that in the gel phase the morphology changes from straight fibrils to frizzy fibrils with the increase in n, whereas in the sol phase the formation of the sheet-like, two-dimensional aggregate is recognized. When the cyclohexane 1(10) gel was photoirradiated (lambda > 300 nm), the UV-VIS absorption bands assignable to monomeric anthracene were decreased and the gel was changed into the sol. It was confirmed by dark-field optical microscopy that the fibrillar bundles supporting the gel formation gradually disappear with photoirradiation time. When this sol was warmed at 30 degrees C in the dark, the gel was not regenerated but the precipitation of 1(10) resulted. When this sol was heated once at the bp of cyclohexane and cooled to 15 degrees C, the solution was changed into the gel again. This finding indicates that the fibrillar structure required for the gel formation is not reconstructed at 30 degrees C but obtained only when the hot cyclohexane solution is cooled. 相似文献
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Mutsumi Sada Dr. Taniyuki Furuyama Dr. Shinsuke Komagawa Prof. Dr. Masanobu Uchiyama Prof. Dr. Seijiro Matsubara 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(34):10474-10481
1,4‐Addition of bis(iodozincio)methane to simple α,β‐unsaturated ketones does not proceed well; the reaction is slightly endothermic according to DFT calculations. In the presence of chlorotrimethylsilane, the reaction proceeded efficiently to afford a silyl enol ether of β‐zinciomethyl ketone. The C? Zn bond of the silyl enol ether could be used in a cross‐coupling reaction to form another C? C bond in a one‐pot reaction. In contrast, 1,4‐addition of the dizinc reagent to enones carrying an acyloxy group proceeded very efficiently without any additive. In this case, the product was a 1,3‐diketone, which was generated in a novel tandem reaction. A theoretical/computational study indicates that the whole reaction pathway is exothermic, and that two zinc atoms of bis(iodozincio)methane accelerate each step cooperatively as effective Lewis acids. 相似文献
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Oneyama C Agatsuma T Kanda Y Nakano H Sharma SV Nakano S Narazaki F Tatsuta K 《Chemistry & biology》2003,10(5):443-451
The proline-rich motif in proteins is known to function as a ligand sequence that binds to protein modules such as SH3, WW, and several other protein interaction domains. These proline-rich ligand-mediated protein-protein interactions (abbreviated PLPI) are important in many signaling pathways that are involved in various diseases. Our previous studies showed that UCS15A, produced by Streptomyces species, inhibited PLPI. Here we report on synthetic analogs of UCS15A that show more potent activity than UCS15A in inhibiting PLPI. A synthetic analog, compound 2c, blocked in vitro PLPI of Sam68-Fyn-SH3 as well as in vivo PLPI of Grb2-Sam68 and Grb2-Sos1. Activation of MEK was also inhibited by compound 2c. Unlike UCS15A, compound 2c was an order of magnitude less cytotoxic and did not cause morphological changes in treated cells. 相似文献
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F. Caccavale C. Sada F. Segato B. Allieri L. E. Depero L. Sangaletti V. A. Fedorov Yu. N. Korkishko T. V. Morozova 《Journal of Non》2001,280(1-3):156-163
Erbium-doped lithium niobate (LiNbO3) crystals were produced by Er–Li ion exchange (IE) process. The role of the process parameters such as exchange time and temperature, crystal cut direction, composition and heating rate of the Er ions liquid source was investigated by means of secondary ion mass spectrometry, X-ray diffraction (XRD) and microluminescence techniques. We demonstrated that Er effective diffusion coefficient is two orders of magnitude greater with respect to the thermal diffusion from Er film. We observed that no Li deficient phase can be achieved and that active Er ions are homogeneously incorporated in the substrate. The method is suitable for Er doping of LiNbO3 crystals at relative low temperature (from 570°C to 650°C). 相似文献
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Sugikawa K Numata M Kinoshita D Kaneko K Sada K Asano A Seki S Shinkai S 《Organic & biomolecular chemistry》2011,9(1):146-153
Creation of higher-ordered polymeric architectures composed of alternative assemblies of single-walled carbon nanotubes (SWNTs) and fibrous porphyrin J-aggregates can be easily achieved utilizing the cationic semi-artificial polysaccharide which can act not only as a tubular host for SWNTs but also as a one-dimensional template for porphyrin molecules. This new class of hierarchical polymer assembly is formed, for the first time, by the mutual template effect of two components, i.e., the cationic SWNT complexes and the anionic porphyrin supramolecular nanofibers. In the present system, the self-assembling behaviors of the SWNT complexes as well as the final properties of the SWNT nanoarchitectures are strongly affected by the packing mode of porphyrin molecules on the cationic semi-artificial polysaccharide. Furthermore, we have confirmed that the light energy captured by the porphyrin J-aggregates is effectively transferred to SWNTs. 相似文献
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Akio Ojida Yoshifumi Miyahara Jirarut Wongkongkatep Shun‐ichi Tamaru Kazuki Sada Itaru Hamachi 《化学:亚洲杂志》2006,1(4):555-563
Nucleoside pyrophosphate (nucleoside PP) derivatives are widespread in living cells and play pivotal roles in various biological events. We report novel fluorescence chemosensors for nucleoside PPs that make use of coordination chemistry. The chemosensors, which contain two ZnII–dipicolylamine units, bind strongly to nucleoside PPs (Kapp>106 M ?1) in aqueous solution and sense them by a dual‐emission change. Detailed fluorescence and UV/Vis spectral studies revealed that the emission changes of the chemosensors upon binding to nucleoside PPs can be ascribed to the loss of coordination between ZnII and the acridine fluorophore. This is a unique sensing system based on the anion‐induced rearrangement of the coordination. Furthermore, we demonstrated the utility of these chemosensors in real‐time monitoring of two important biological processes involving nucleoside PP conversion: the apyrase‐catalyzed hydrolysis of nucleoside PPs and the glycosyl transfer catalyzed by β‐1,4‐galactosyltransferase. 相似文献