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61.
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Yashima M Enoki M Wakita T Ali R Matsushita Y Izumi F Ishihara T 《Journal of the American Chemical Society》2008,130(9):2762-2763
MEM nuclear density analysis from neutron diffraction data measured in situ at 1015.6 degrees C has indicated the two-dimensional network of curved O2-O3-O2 oxide-ion diffusion paths on the (Pr,La)-O layer in a K2NiF4-type structured oxide-ionic and electronic mixed conductor (Pr0.9La0.1)2(Ni0.74Cu0.21Ga0.05)O4+delta. 相似文献
63.
A Tin Analogue of Carbenoid: Isolation and Reactivity of a Lithium Bis(imidazolin‐2‐imino)stannylenoid 下载免费PDF全文
Tatsumi Ochiai Dr. Daniel Franz Dr. Xiao‐Nan Wu Dr. Elisabeth Irran Prof. Dr. Shigeyoshi Inoue 《Angewandte Chemie (International ed. in English)》2016,55(24):6983-6987
The lithium bis(imino)stannylenoid (NIPr)2Sn(Li)Cl ( 1 ; NIPr=bis(2,6‐diisopropylphenyl)imidazolin‐2‐imino) was prepared by the reaction of LiNIPr with 0.5 equiv of SnCl2?diox (diox=1,4‐dioxane) and the ambiphilic character of the compound was demonstrated by investigations into its reactivity. Treatment of 1 with I2 or MeI yielded the oxidative addition products (NIPr)2SnI2 and (NIPr)2Sn(Me)I, respectively. In contrast, the reaction of 1 with one equivalent of Me3SiCl resulted in the formation of Me3SiNIPr and the chlorostannylene dimer [NIPrSnCl]2. Moreover, the substitution reaction of compound 1 with MeLi led to the formation of the methyl‐substituted stannate (NIPr)2Sn(Li)Me. 相似文献
64.
Application to Photocatalytic H2 Production of a Whole‐Cell Reaction by Recombinant Escherichia coli Cells Expressing [FeFe]‐Hydrogenase and Maturases Genes 下载免费PDF全文
Dr. Yuki Honda Prof. Hidehisa Hagiwara Prof. Shintaro Ida Prof. Tatsumi Ishihara 《Angewandte Chemie (International ed. in English)》2016,55(28):8045-8048
A photocatalytic H2 production system using an inorganic–bio hybrid photocatalyst could contribute to the efficient utilization of solar energy, but would require the development of a new approach for preparing a H2‐forming biocatalyst. In the present study, we constructed a recombinant strain of Escherichia coli expressing the genes encoding the [FeFe]‐hydrogenase and relevant maturases from Clostridium acetobutylicum NBRC 13948 for use as a biocatalyst. We investigated the direct application of a whole‐cell of the recombinant E. coli. The combination of TiO2, methylviologen, and the recombinant E. coli formed H2 under light irradiation, demonstrating that whole cells of the recombinant E. coli could be employed for photocatalytic H2 production without any time‐consuming and costly manipulations (for example, enzyme purification). This is the first report of the direct application of a whole‐cell reaction of recombinant E. coli to photocatalytic H2 production. 相似文献
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Nagamatsu S Misaki M Chikamatsu M Kimura T Yoshida Y Azumi R Tanigaki N Yase K 《The journal of physical chemistry. B》2007,111(17):4349-4354
Poly(2,5-dioctyloxy-1,4-phenylenevinylene) (DOPPV) was found to form a highly oriented film by a friction-transfer technique. Structural investigation of friction-transferred DOPPV was studied by means of polarized ultraviolet-visible (UV-vis) absorption spectroscopy, polarized photoluminescence (PL) spectroscopy, and synchrotron-sourced grazing incident X-ray diffraction (GIXD) analysis. The polarized UV-vis absorption and PL spectra indicate clear axial alignment. DOPPV backbones in friction-transferred film are highly aligned along the drawing direction of the friction-transfer. Further information of the molecular arrangement in friction-transferred DOPPV film was investigated by both the out-of-plane and the in-plane GIXD analyses with synchrotron source. The DOPPV molecules in friction-transferred films were perfectly arranged three-dimensionally: the backbones aligned along the drawing direction of friction-transfer, the alkyl side chains lay in the film plane, and the planar backbones were arranged parallel to the film surface. Additionally, two neighboring DOPPV molecules along the direction of inter-backbones separation by alkyl side chains were found to be shifted with respect to one another by the mean distance of half of a monomeric repeat. 相似文献
67.
Tatsumi Ochiai Dr. Daniel Franz Dr. Elisabeth Irran Prof. Dr. Shigeyoshi Inoue 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(18):6704-6707
The novel amino(imino)stannylene 1 was prepared by conversion of HNIPr (NIPr=bis(2,6‐diisopropylphenyl)imidazolin‐2‐imino) with one equivalent of Lappert’s tin reagent (Sn[N(SiMe3)2]2). Treatment of 1 with DMAP (4‐dimethylaminopyridine) yields its Lewis acid–base adduct 2 . The reaction of 1 with one equivalent of trimethylsilyl azide results in replacement of the amino group at the tin center by an N3 substituent with concomitant elimination of N(SiMe3)3 to afford dimeric [N3SnNIPr]2 ( 3 ). Remarkably, the reaction of 1 with B(C6F5)3 produces the novel tin(II) monocation 4 +[MeB(C6F5)3]? comprising a four‐membered stannacycle through methyl‐abstraction from the trimethylsilyl group. 相似文献
68.
Mayumi Sakamoto Gerald Kehr Kazuyuki Tatsumi 《Journal of organometallic chemistry》2009,694(17):2820-4038
Coordinatively unsaturated rhodium and iridium complexes having a bulky thiolate, [Cp∗M(PMe3)(SDmp)](BArF4) (1a: M = Rh; 1b: M = Ir; Dmp = 2,6-(mesityl)2C6H3, ArF = 3,5-(CF3)2C6H3), catalyzed the hydrogenation of benzaldehyde, N-benzylideneaniline, and cyclohexanone, under 1 atm of H2 at low temperatures. In these catalytic reactions, the M-H/S-H complexes [Cp∗M(PMe3)(H)(HSDmp)](BArF4) (2a: M = Rh; 2b: M = Ir) generated via H2 heterolysis by 1a or 1b were suggested to transfer both M-H hydride and S-H proton to substrates. The catalytic reactions were terminated by the dissociation of H-SDmp from the metal centers of 2a and 2b that occurs at ambient temperature under H2 atmosphere. 相似文献
69.
The evolution of the microstructure and rheological properties of plate-like particle suspensions subjected to rapid simple shear is studied numerically. In response to the shear-induced strain, particles in the suspensions rearrange to form a steady-state microstructure, and the suspension viscosity reaches a steady value. Under this condition, the microstructure is composed of two domains having different particle fractions and particle orientations. In the matrix (particle-poor) and cluster (particle-rich) domains, the particles’ long axes are oriented subparallel to the shear plane and normal to the maximum compressive principal direction, respectively. A higher particle concentration and friction coefficient enhance the development of cluster domains relative to matrix domains leading the intensity of the preferred particle orientation to decrease and the number of contacting particles, the aspect ratio of clusters, the inter-particle force, and the suspension viscosity to increase. The domain microstructure is governed by two factors: (1) geometric relations between the particle orientation and the maximum compressive axes and (2) the magnitude of particle–fluid and particle–particle interactions. The first factor results in the coupling of the particle orientation and the local fraction of particles, which is an important character of the domain microstructure. The second factor controls the relative development of the cluster and matrix domains through the change in the particles’ rotational behavior. Our results suggest that the microstructure of plate-like suspensions subjected to rapid shear is predictable in terms of the cluster stability, which has important implications for the kinematics of flow-related microstructures in nature and manufacturing. 相似文献
70.