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91.
We demonstrate that if k-essence can solve the coincidence problem and play the role of dark energy in the Universe, the fluctuations of the field have to propagate superluminally at some stage. We argue that this implies that successful k-essence models violate causality. It is not possible to define a time ordered succession of events in a Lorentz invariant way. Therefore, k-essence cannot arise as a low energy effective field theory of a causal, consistent high energy theory. 相似文献
92.
Camille Pouchol 《Comptes Rendus Mathematique》2018,356(6):644-647
We consider the non-local Fisher–KPP equation on a bounded domain with Neumann boundary conditions. Thanks to a Lyapunov function, we prove that, under a general hypothesis on the kernel involved in the non-local term, the homogenous steady state 1 is globally asymptotically stable. This assumption happens to be linked to some conditions given in the literature, which ensure that travelling waves link 0 to 1. 相似文献
93.
Bernhard Schnenberger Walter Summermatter Camille Ganter 《Helvetica chimica acta》1982,65(7):2333-2337
An enantioselective synthesis of key intermediates for the synthesis of the anti-microbially active pseudomonic acids A ( 1 ), B ( 2 ) and C ( 3 ) is described. D -Ribose ( 4 ) was used as starting material. 相似文献
94.
Joyce MJ Sharpey-Schafer JF Twin PJ Beausang CW Cullen DM Riley MA Clark RM Dagnall PJ Deloncle I Duprat J Fallon P Forsyth PD Fotiades N Gale SJ Gall B Hannachi F Harissopulos S Hauschild K Jones PM Kalfas CA Korichi A Le Coz Y Meyer M Paul ES Porquet MG Redon N Schuck C Simpson J Vlastou R Wadsworth R 《Physical review letters》1993,71(14):2176-2179
95.
Janaina C. Bataglioli Luiza M. F. Gomes Camille Maunoir Jason R. Smith Houston D. Cole Julia McCain Tariq Sainuddin Colin G. Cameron Sherri A. McFarland Tim Storr 《Chemical science》2021,12(21):7510
Alzheimer''s disease (AD) is a chronic neurodegenerative disorder characterized by progressive and irreversible damage to the brain. One of the hallmarks of the disease is the presence of both soluble and insoluble aggregates of the amyloid beta (Aβ) peptide in the brain, and these aggregates are considered central to disease progression. Thus, the development of small molecules capable of modulating Aβ peptide aggregation may provide critical insight into the pathophysiology of AD. In this work we investigate how photoactivation of three distorted Ru(ii) polypyridyl complexes (Ru1–3) alters the aggregation profile of the Aβ peptide. Photoactivation of Ru1–3 results in the loss of a 6,6′-dimethyl-2,2′-bipyridyl (6,6′-dmb) ligand, affording cis-exchangeable coordination sites for binding to the Aβ peptide. Both Ru1 and Ru2 contain an extended planar imidazo[4,5-f][1,10]phenanthroline ligand, as compared to a 2,2′-bipyridine ligand for Ru3, and we show that the presence of the phenanthroline ligand promotes covalent binding to Aβ peptide His residues, and in addition, leads to a pronounced effect on peptide aggregation immediately after photoactivation. Interestingly, all three complexes resulted in a similar aggregate size distribution at 24 h, forming insoluble amorphous aggregates as compared to significant fibril formation for peptide alone. Photoactivation of Ru1–3 in the presence of pre-formed Aβ1–42 fibrils results in a change to amorphous aggregate morphology, with Ru1 and Ru2 forming large amorphous aggregates immediately after activation. Our results show that photoactivation of Ru1–3 in the presence of either monomeric or fibrillar Aβ1–42 results in the formation of large amorphous aggregates as a common endpoint, with Ru complexes incorporating the extended phenanthroline ligand accelerating this process and thereby limiting the formation of oligomeric species in the initial stages of the aggregation process that are reported to show considerable toxicity.Photoactivation of a series of Ru(ii) polypyridyl complexes leads to ligand exchange and modulation of amyloid-beta peptide aggregation of relevance to Alzheimer''s disease. 相似文献
96.
(+)-(1S, 3S, 6S, 8S)-and (?)-(1R, 3R, 6R, 8R)-4, 9-Twistadiene: Synthesis and Absolute Configuration A synthesis and the determination of the absolute configuration of (+)-(1S, 3S, 6S, 8S)- and (?)-(1R, 3R, 6R, 8R)-4, 9-twistadiene ((+)- and (?)- 4 , respectively) is described. Their chiroptical properties are compared with those of saturated twistane ((+)- and (?)- 5 ) as well as with those of the unsaturated and saturated 2, 7-dioxatwistane analogs (+)- and (?)- 9 , and (+)- and (?)- 10 , respectively, which also are compounds of known absolute configurations. 相似文献
97.
Duygu Avci Camille Haynes Lon J. Mathias 《Journal of polymer science. Part A, Polymer chemistry》1997,35(10):2111-2121
New diacrylate monomers for cyclopolymerization were synthesized from the reaction of ethyl α-chloromethylacrylate (ECMA) and t-butyl α-bromomethyl acrylate (TBBr) with aniline, adamantyl amine, t-butyl amine, cyanamide, and 4-tetradecyl aniline in yields of ca. 50–70%. Bulk and solution polymerizations with azobisisobutyronitrile (AIBN) at 60–85°C gave soluble cyclopolymers with Mn and Mw ranging from 10,000–30,000 and 12,000–40,000, respectively. The ECMA–cyanamide derivative only gave crosslinked polymers. 1H and 13C solution NMR indicated high cyclization efficiency (>93%). A prototype NLO polymer was synthesized from the reaction of the TBBr–aniline cyclopolymer with tetracyanoethylene. The p-hydroxyaniline derivative of ECMA was synthesized and used for further derivatizations; for example, the benzoate ester was made and polymerized (Mn = 21,260 and Mw = 40,317). The ester groups of the TBBrndash;aniline polymer were hydrolyzed completely to give a polymer with both acid and base moieties. DSC thermograms showed glass transitions of 132°C for the ECMA–aniline derivative, 192°C for the ECMA–adamantyl derivative, 53°C for the TBBr–tetradecylaniline derivative, and 120° for the ECMA–p-benzoylaniline derivative. The ECMA–t-butyl amine polymer showed no obvious Tg. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 2111–2121, 1997 相似文献
98.
99.
A mechanistic model is presented for the base‐catalyzed intramolecular cyclization of polycyclic unsaturated alcohols of type A to ethers D (Scheme 1). The alkoxide anion B is formed first in a fast acid‐base equilibrium. For the subsequent reaction to D , a carbanion‐like transition state C is proposed. This mechanism is in full agreement with our results regarding the influence of substituents on the regioselectivity and the rate of cyclization. We studied the effect of alkyl substituents in allylic position (alkylated endocylic olefinic alcohols 1 – 3 ) and, especially, at the exocyclic double bond ( 12 – 15 ). The fastest cyclization (krel=1) is 12 → 16 , which proceeds via a primary carbanion‐like transition state ( E : R1=R2=H). The corresponding processes 13 → 17 and 14 → 17 are characterized by a less‐stable secondary carbanion‐like transtition state ( E : R1=Me, R2=H, or vice versa) and are slower by a factor of 104. The slowest reaction (krel ca. 10−6) is the cyclization 15 → 18 via a tertiary carbanion‐like transition state ( E : R1=R2=Me). 相似文献
100.
N. Buforn A. Astier J. Meyer M. Meyer S. Perriès N. Redon O. Stézowski M.G. Porquet I. Deloncle A. Bauchet J. Duprat B.J.P. Gall C. Gautherin E. Gueorguieva F. Hoellinger T. Kutsarova R. Lucas A. Minkova N. Schulz H. Sergolle Ts. Venkova A.N. Wilson 《The European Physical Journal A - Hadrons and Nuclei》2000,7(3):347-353
High-spin states in 113-116Cd have been investigated with the fusion-fission reaction 28Si +176Yb at 145 > MeV. The experiment has been performed with the Eurogam2 array. New rotational bands based on two quasi-particle
states have been observed for even-even cadmium isotopes. A new level scheme based on the 11/2− isomeric state is proposed for 115Cd and the one of 113Cd has been extended to spin (31/2−). The decoupled bands identified in both odd-A nuclei are interpreted as being built upon a low-Ωh11/2 quasi-neutron configuration. Microscopic Hartree-Fock + BCS calculations confirm the prolate deformation in this mass region
especially for the odd cadmium isotopes.
Received: 21 December 1999 / Revised version: 16 February 2000 相似文献