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排序方式: 共有103条查询结果,搜索用时 15 毫秒
51.
Hongting Jia Kiyotoshi Yasumoto 《International Journal of Infrared and Millimeter Waves》2005,26(9):1291-1306
A new approach for modal analysis of coupled cavity waveguides (CCW) in two-dimensional photonic crystals is presented. The mode propagation constants and the mode field profiles can be accurately derived by a simple matrix calculation, using a one-dimensional lattice sums, a T-matrix of an isolated circular cylinder, and generalized reflection matrices. Numerical examples have confirmed that the convergence of numerical solutions is very fast and the accuracy is very high.* Supported by the 21st Century
COE Program “Reconstruction of Social Insfrastructure Related to
Information Science and Electrical Engineerings”. 相似文献
52.
Kazuhiro Yasumoto Tomohisa Norisuye Yusuke Teranishi Qui Tran‐Cong‐Miyata Shigeki Nomura 《Journal of polymer science. Part A, Polymer chemistry》2012,50(16):3295-3302
Sol–gel derived organic–inorganic hybrids containing phosphotungstic acid (PWA) have been prepared previously to obtain proton conductive membranes. However, leaking of PWA was a serious problem to achieve the higher proton conductivity. In this study, polyelectrolyte membranes functionalized with sulfonic acid groups were fabricated by the sol–gel method. Proton conductivity measurements were performed on an impedance analyzer at 80°C/95% RH. The functionalized polyelectrolyte membranes exhibited the proton conductivity σ ~ 0.9 (S/cm) which was much higher than the previously reported hybrids containing PWA. Although the hybrids exhibited fairly high proton conductivity irrespective to the catalysts used, that under the low relative humidity strongly depends on the catalysts. Among the hybrids prepared in this study, the membrane synthesized with HCl showed outstanding proton conductive properties even at the low humidity thanks to the proton transport channel formed by the swelling of ionic clusters. This fact was confirmed by measuring the ion exchange capacity, water uptake, swelling rate, Fourier transform infrared spectroscopy, atomic force microscopy, and thermogravimetric analysis. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
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54.
Chimeric RNA Oligonucleotides with Triazole and Phosphate Linkages: Synthesis and RNA Interference
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Dr. Tomoko Fujino Kanako Kogashi Koudai Okada Dr. Martin Mattarella Takeru Suzuki Dr. Kenichi Yasumoto Prof. Kazuhiro Sogawa Prof. Hiroyuki Isobe 《化学:亚洲杂志》2015,10(12):2683-2688
Chimeric RNA oligonucleotides with an artificial triazole linker were synthesized using solution‐phase click chemistry and solid‐phase automated synthesis. Scalable synthesis methods for jointing units for the chimeric structure have been developed, and after click‐coupling of the jointing units with triazole linkers, a series of chimeric oligonucleotides was prepared by utilizing the well‐established phosphoramidite method for the elongation. The series of chimeric 21‐mer oligonucleotides that possessed the triazole linker at different strands and positions allowed for a screening study of the RNA interference to clarify the preference of the triazole modifications in small‐interfering RNA molecules. 相似文献
55.
Inside Cover: Chimeric RNA Oligonucleotides with Triazole and Phosphate Linkages: Synthesis and RNA Interference (Chem. Asian J. 12/2015)
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56.
Here we describe catalytic asymmetric synthesis of α-(trifluoromethyl)benzylamine (1) via biomimetic transamination using chiral base. Imine 4 was isomerized to Schiff base 5 using 50 mol.% of cinchonidine derivatives as a catalyst in chloroform, methanol or acetonitrile. In the case of cinchonidine 6 as a catalyst, the reaction conducted in chloroform allowed for 79% conversion of the starting imine 4 in 52 days. The product imine 5 was obtained of (R) absolute configuration in 35% ee as individual compound without any byproducts. The catalyst 6 can be recovered (>95%) by adding n-hexane to the reaction mixture followed by a simple filtration. 相似文献
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58.
K J James A G Bishop R Draisci L Palleschi C Marchiafava E Ferretti M Satake T Yasumoto 《Journal of chromatography. A》1999,844(1-2):53-65
Two acidic analogues of the polyether marine toxin, pectenotoxin-2 (PTX-2), responsible for diarrhetic shellfish poisoning (DSP), have been isolated from the toxic marine phytoplankton (Dinophysis acuta), collected in Irish waters. Liquid chromatography with fluorimetric detection (LC-FLD) analyses of the extracts of bulk phytoplankton samples, following derivatisation with 9-anthryldiazomethane (ADAM) or 1-bromoacetylpyrene (BAP), showed a complex toxin profile with peaks corresponding to okadaic acid (OA) and its isomers, dinophysistoxin-2 (DTX-2) and DTX-2C, as well as other unidentified lipophilic acids. LC-UV analysis showed the presence of a diene moiety in these new compounds and two acids have been isolated. LC coupled with mass spectrometry (MS) and tandem mass spectrometry (LC-MS-MS) were used to gain structural information. Through flow injection analysis (FIA)-MS, both in positive and negative ion modes, the molecular weight of 876 for both compounds was determined. Collision Induced Dissociation (CID) from each parent ion, as performed both in positive and negative ion mode, produced mass spectra which were very similar to those obtained for authentic PTX-2 (mw 858). These new compounds have been confirmed to be pectenotoxin-2 seco acids (PTX-2SAs) and they are closely related to PTX-2 except that they contain an open chain carboxylic acid rather than a lactone ring. Toxic mussels also contained these pectenotoxin-2 analogues. 相似文献
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60.
Hideaki Uchida Yohsuke Taira Takeshi Yasumoto 《Rapid communications in mass spectrometry : RCM》2013,27(17):1999-2008