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81.
82.
We investigated the electro-optic (EO) response of a reflective planar microcavity with a poled polymer spacer using reflection ellipsometry. We designed and fabricated the microcavity to have an enhanced local field in the EO polymer spacer and evaluated the resulting enhancement in the voltage-induced phase difference between the s- and p-polarized components. The phase difference obtained was 56 times larger than that for the EO polymer alone. This enhancement is attributed to the polarization-dependent local field effect for oblique incidence. 相似文献
83.
On-chip fluorescence determination of sulfite and nitrite with N-(9-acridinyl)maleimide (NAM) and 2,3-diaminonaphthalene (DAN) has been developed using a novel fluorescence detection unit for microchip analysis. Usually, these fluorescence reagents are derivatized and detected separately in microchip analysis because different fluorescence wavelengths are emitted. The proposed fluorescence detection unit has optical fibers with no optical filter, and plural wavelengths of fluorescence were detected sensitively, even in the microchip. In this study, the simultaneous determination of sulfite and nitrite in environmental samples was performed with a polymer microchip analysis system. The calibration curves of sulfite and nitrite showed linear relations (R2 = 0.998 (sulfite) and R2 = 0.990 (nitrite)), and the relative standard deviations (RSD) for 4 runs were 2.1% (20 microM sulfite) and 1.3% (20 microM nitrite), respectively. The proposed method was applied to the recovery test of sulfite and nitrite in environmental samples. 相似文献
84.
Prof. Ryo Ohtani Hiromu Matsunari Prof. Takafumi Yamamoto Prof. Koji Kimoto Prof. Masaaki Isobe Dr. Kotaro Fujii Prof. Masatomo Yashima Dr. Susumu Fujii Dr. Akihide Kuwabara Dr. Yuh Hijikata Prof. Shin-ichiro Noro Prof. Masaaki Ohba Prof. Hiroshi Kageyama Prof. Shinya Hayami 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(43):19416-19421
Metal node design is crucial for obtaining structurally diverse coordination polymers (CPs) and metal–organic frameworks with desirable properties; however, FeII ions are exclusively six-coordinated. Herein, we present a cyanide-bridged three-dimensional (3D) CP, FePd(CN)4, bearing four-coordinate FeII ions, which is synthesized by thermal treatment of a two-dimensional (2D) six-coordinate FeII CP, Fe(H2O)2Pd(CN)4⋅4 H2O, to remove water molecules. Atomic-resolution transmission electron microscopy and powder X-ray and neutron diffraction measurements revealed that the FePd(CN)4 structure is composed of a two-fold interpenetrated PtS topology network, where the FeII center demonstrates an intermediate geometry between tetrahedral and square-planar coordination. This four-coordinate FeII center with the distorted geometry can act as a thermo-responsive flexible node in the PtS network. 相似文献
85.
Yoshihiro Shigemasa Shin-ichiro Tanioka Hiroyuki Furukawa Hitoshi Sashiwa Hiroyuki Saimoto 《Journal of carbohydrate chemistry》2013,32(1):97-100
ABSTRACT The “formose reaction” is the generic name for the base-catalyzed condensation of formaldehyde to give “formose” which is a complex mixture of sugars, alditols, organic acids, etc.2 Increasing attention has been recently given to this reaction because of its possible importance in the manufacture of edible carbohydrates from a simple material and its possible role in the prebiotic synthesis of carbohydrates.3 In our recent study4 on the reaction catalyzed by triethylamine (TEA) and thiamine HCl in N,N-dimethylformamide (DMF)-water mixed solvent, the formation of 3-pentulose (GP-11-1 corresponding to GLC peak number 11-1) was suggested. P. Decker et al.5 also reported that at the end of formaldehyde consumption the concentration of 3-pentuloses became smaller because of their higher reactivity (these carbohydrates cannot form stable furanoses or pyranoses) compared to tetroses, pentoses, and hexoses. Although the isolation of 3-pentuloses was not described in that report,5 erythro-3-pentulose and threo-3-pentulose in a formose were identified by comparison of GLC retention times and mass spectra with those of authentic samples. 相似文献
86.
Shin-ichiro Sakurai Akihiro Ohira Yoshinori Suzuki Riri Fujito Tatsuya Nishimura Masashi Kunitake Eiji Yashima 《Journal of polymer science. Part A, Polymer chemistry》2004,42(18):4621-4640
Novel sets of helical poly(phenylacetylene)s bearing a chiral ruthenium (Ru) complex with opposite chirality (Δ and Λ forms) as a bulky pendant (poly- 1 and poly- 2 ) were synthesized through the polymerization of the corresponding optically pure phenylacetylenes with a rhodium catalyst, and their structures in solution and morphology on solid substrates were investigated with NMR, ultraviolet–visible, and circular dichroism (CD) spectroscopies and with atomic force microscopy (AFM), respectively. The obtained cis–transoidal polymers (poly- 1 and poly- 2 ) showed characteristic Cotton effects in the region of metal-to-ligand charge transfer of the chiral Ru pendants. Poly- 1 and poly- 2 were thought to have a predominantly one-handed helical conformation induced by the chiral pendants. However, the apparent Cotton effects derived from the helically twisted π-conjugated polymer backbone could not be observed, probably because of the strong chiral chromophoric pendants. However, in the AFM images, the helical polymers adsorbed on mica could be easily discerned as isolated strands, and the visualization and discrimination of the right- and left-handed helical structures of the chiral polymers were achieved by high-resolution AFM imaging. On the basis of the AFM observations together with the CD measurements and computational calculation results, possible structures of poly- 1 and poly- 2 were examined. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4621–4640, 2004 相似文献
87.
Endo T Akutagawa T Noro S Nakamura T 《Dalton transactions (Cambridge, England : 2003)》2011,40(7):1491-1496
A supramolecular cation of (m-FAni(+))(DB[18]crown-6), where m-FAni(+) and DB[18]crown-6 denote m-fluoroanilinium(+) and dibenzo[18]crown-6, respectively, which is the polar unit rotating in the ferroelectric crystal of (m-FAni(+))(DB[18]crown-6)[Ni(dmit)(2)](-), was introduced into a ferromagnetic [MnCr(oxalate)(3)](-) salt as the counter cation. The crystal structure of (m-FAni(+))(DB[18]crown-6)[MnCr(oxalate)(3)](-)(CH(3)OH)(CH(3)CN) (1) is constructed from alternating layers of a two-dimensional honeycomb layer of [MnCr(oxalate)(3)](-) and (m-FAni(+))(DB[18]crown-6) supramolecular cations. The anionic layer is composed of Mn(II) and Cr(III) ions with S = 5/2 and S = 3/2 spins, respectively, bridged by the oxalate anions, which show ferromagnetic ordering at 5.5 K. The supramolecular structure is formed through the formation of hydrogen bonds between the ammonium hydrogen atoms of the m-FAni(+) cations and the oxygen atoms of the DB[18]crown-6 cavity. No orientational disorder of the fluorine atoms was observed in our X-ray structural analysis, suggesting that a two-fold flip-flop motion of the m-FAni(+) cations does not occur in the salt. The rotational freedom of the m-FAni(+) cations in the salt is restricted by the steric hindrance from neighbouring DB[18]crown-6 molecules. A design strategy for the rotation in a salt is discussed, based on the volume that the supramolecular cations occupy in the unit cell. 相似文献
88.
Hidetsura Cho Eunsang Kwon Yoshizumi YasuiSatoshi Kobayashi Shin-ichiro Yoshida Yoshio Nishimura Masahiko Yamaguchi 《Tetrahedron letters》2011,52(52):7185-7188
The first observation of ring cleavage between positions 1 and 2 of a 1,4-dihydropyrimidine skeleton was reported upon the nucleophilic addition of 4,6-unsubstituted 1,4-dihydropyrimidine with 3 equiv of an aniline derivative or phenylhydrazine in the presence of 0.1 equiv of pyridinium p-toluenesulfonate (PPTS) in CH2Cl2; the nucleophilic reactions of 4-methyl-6-unsubstituted 1,6(3,4)-dihydropyrimidine with the same amines gave conventional substituted products at position 2. The effect of this ring opening was found to be due to the electron density of the benzene ring of a nucleophilic amine. On the other hand, aralkylamines, alkylamines, or heterocyclic amines did not cleave the skeleton. The ring-opening chemical structure was confirmed by X-ray crystallographic analysis. This characteristically different phenomenon may be due to the pattern of two CC double bonds of 1,4-DP and 1,6(3,4)-DP as well as to the effect of two substituted groups on the DP ring. 相似文献
89.
Shin-ichiro Mizumoto 《Journal of Number Theory》2004,105(1):134-149
For j=1,…,n let fj(z) and gj(z) be holomorphic modular forms for such that fj(z)gj(z) is a cusp form. We define a series
90.
Shiro Goto Futoshi Hayasaka Shin-ichiro Iai 《Proceedings of the American Mathematical Society》2003,131(1):87-94
Let be a regular local ring and let be a filtration of ideals in such that is a Noetherian ring with . Let and let be the -invariant of . Then the theorem says that is a principal ideal and for all if and only if is a Gorenstein ring and . Hence , if is a Gorenstein ring, but the ideal is not principal.