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排序方式: 共有153条查询结果,搜索用时 31 毫秒
41.
Abrams GS Adolphsen CE Averill D Ballam J Barish BC Barklow T Barnett BA Bartelt J Bethke S Blockus D Bonvicini G Boyarski A Brabson B Breakstone A Bulos F Burchat PR Burke DL Cence RJ Chapman J Chmeissani M Cords D Coupal DP Dauncey P DeStaebler HC Dorfan DE Dorfan JM Drewer DC Elia R Feldman GJ Fernandes D Field RC Ford WT Fordham C Frey R Fujino D Gan KK Gero E Gidal G Glanzman T Goldhaber G Gomez Cadenas JJ Gratta G Grindhammer G Grosse-Wiesmann P Hanson G Harr R Harral B Harris FA 《Physical review letters》1989,63(22):2447-2451
42.
Bonvicini G Gero E Frey R Koska W Field C Phinney N Minten A 《Physical review letters》1989,62(20):2381-2384
43.
Dagny D. Konieczna Harry Biller Matthias Witte Wolf Gero Schmidt Adam Neuba René Wilhelm 《Tetrahedron》2018,74(1):142-149
The presented work comprised the synthesis and characterization of new ionic organic dyes as potential photosensitizer (PS) in the photocatalytic H2 evolution reaction. The presented dyes are consisting of donor-π-acceptor (D-π-A) structures that are commonly used for organic dyes for organic solar cells. The acceptor is based on a cationic pyridinium moiety. Furthermore, a complex was synthesized, in which a D-π-A photosensitizer is linked as ligand to cobaloxime. The latter is a common proton reduction catalyst. The attached ligand enabled a fast intramolecular electron transfer to the cobalt center. The resulted complex showed high stability and potential in the homogeneous photocatalytic H2 evolution reaction. Finally, one ionic dye showed a high activity when combined with TiO2 and Pt in a heterogeneous hydrogen evolution reactions with a TOF of up to 407 h?1. 相似文献
44.
Gero P. Hooff Nina Patel W. Gibson Wood Walter E. Müller Gunter P. Eckert Dietrich A. Volmer 《Analytical and bioanalytical chemistry》2010,398(4):1801-1808
The isoprenoids farnesyl-(FPP) and geranylgeranylpyrophosphate (FPP and GGPP) are two major lipid intermediates in the mevalonate
pathway. They participate in post-translational modification of members of the superfamily of small guanosine triphosphatases
(GTPases; Ras, Rab, Rac, etc.) via prenylation reactions. Due to the important role of these proteins in a number of cell
processes, in particular cell growth, division, and differentiation, investigation of the involvement of isoprenoids in these
processes is of great interest. In a previously published report, we described a fully validated assay for the quantitation
of the two isoprenoids using a high-performance liquid chromatography (HPLC)–fluorescence detection (FLD) method. The current
work expands on the previous method and enhances it greatly by using a much faster state-of-the-art ultrahigh-performance
liquid chromatography (UHPLC) technique coupled to tandem mass spectrometry (MS/MS). The method exhibited a linear concentration
range of 5–250 ng/mL for FPP and GGPP in human brain tissue; it was shown to be unaffected by ion suppression and provided
results almost six times faster than the HPLC–FLD assay. Comparison of UHPLC–MS/MS and HPLC–FLD yielded excellent comparability
of the two assays for both isoprenoids. Based on the UHPLC–MS/MS assay, a novel in vitro test system was implemented to study
enzyme specificity for distinct amino acid CAAX motifs, which is potentially useful for investigating target interactions
of new therapeutics for diseases involving pathological regulation of isoprenoids and/or small GTPases. 相似文献
45.
We demonstrate an extremely accurate method for measuring ultrabroadband, sub-10 fs pulses even if they exhibit a highly modulated spectrum, space-time coupling, or both. The method uses a spatially encoded arrangement for spectral phase interferometry for direct electric field reconstruction, which allows a zero additional phase measurement to be performed with a relatively low signal-to-noise ratio in real time and single shot. 相似文献
46.
L. Castellanos A. Gateau-Olesker F. Panne-Jacolot J. Cleophax S.D. Gero 《Tetrahedron》1981,37(9):1691-1696
Epoxides 7, 8 and 9 have been prepared from d and l-xylose, and used for the synthesis of a precursor of ent-(11-oxa)PG 19 and of 9,13-and 7,11-dioxaprostanoïc acids 28 and 31. The site of the opening of the epoxidcs 7 and 9 with the carbanion derived from bis-(phenylth)romethane and with LiAlH4 is shown by establishing structures of the products 11, 12, 20 et 21 by 13CNMR spectroscopy. 相似文献
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