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101.
We show experimentally that large matrices of localized structures can be stored as elementary pixels in a nematic liquid crystal cell. Based on optical feedback with phase modulated input beam, our system allows us to store, erase, and actualize the localized structures in the matrix. 相似文献
102.
Ricciardi A Pisco M Gallina I Campopiano S Galdi V O' Faolain L Krauss TF Cusano A 《Optics letters》2010,35(23):3946-3948
We report on the first experimental evidence of guided resonances (GRs) in photonic crystal slabs based on aperiodically ordered supercells. Using Ammann-Beenker (quasiperiodic, eightfold symmetric) tiling geometry, we present our study on the fabrication, experimental characterization, and full-wave numerical simulation of two representative structures (with different filling parameters) operating at near-IR wavelengths (1300-1600 nm). Our results show a fairly good agreement between measurements and numerical predictions and pave the way for the development of new strategies (based on, e.g., the lattice symmetry breaking) for GR engineering. 相似文献
103.
Stefania Bellavia Elisa Riccietti 《Journal of Optimization Theory and Applications》2018,178(3):824-859
In this paper, we address the stable numerical solution of ill-posed nonlinear least-squares problems with small residual. We propose an elliptical trust-region reformulation of a Levenberg–Marquardt procedure. Thanks to an appropriate choice of the trust-region radius, the proposed procedure guarantees an automatic choice of the free regularization parameters that, together with a suitable stopping criterion, ensures regularizing properties to the method. Specifically, the proposed procedure generates a sequence that even in case of noisy data has the potential to approach a solution of the unperturbed problem. The case of constrained problems is considered, too. The effectiveness of the procedure is shown on several examples of ill-posed least-squares problems. 相似文献
104.
Michelangelo Iannone Stefania Bulotta Donatella Paolino Maria Cristina Zito Santo Gratteri Francesco S Costanzo Domenicantonio Rotiroti 《BMC neuroscience》2006,7(1):13-6
Background
3,4-Methylenedioxymethamphetamine (MDMA; ecstasy) is known for its toxicological, psychopathological and abuse potential. Some environmental conditions, e.g. acoustic stimulation typical of the "rave scene" can influence the toxicity of this drug. 相似文献105.
Stefania‐Felicia Barbuceanu Gabriela Bancescu Gabriel Saramet Florica Barbuceanu Constantin Draghici Flavian Stefan Radulescu Aura Ionescu Simona Negres 《Heteroatom Chemistry》2013,24(4):309-321
In the present study, new 1,2,4‐triazoles, 1,3,4‐thiadiazoles, and acylthiosemicarbaz‐ides derived from 4‐(4‐chlorophenylsulfonyl)benzoic acid hydrazide were synthesized and screened for their antimicrobial and analgesic activities. Acylthiosemicarbazides 2–4 were synthesized by a reaction of 4‐(4‐chlorophenyl‐sulfonyl)benzoic acid hydrazide 1 with different arylisothiocyanates.4,5‐Disubstituted‐2,4‐dihydro‐3H‐1,2,4‐triazol‐3‐thiones 5–7 and 2,5‐disubstituted‐1,3,4‐thiadiazoles 8–10 were obtained by dehydrative cyclization of corresponding acylthiosemicarbazide derivatives 2–4 in basic media (8% aqueous sodium hydroxide) and in acidic media (sulfuric acid or phosphorous oxychloride), respectively. The structures of the newly synthesized compounds have been confirmed on the basis of elemental analysis and spectral studies (IR, 1H NMR, 13C NMR, MS). Their antimicrobial activities against some bacteria and yeasts were investigated. The analgesic activity of all compounds was performed with two pharmacological tests: the writhing test induced with acetic acid and hot‐plate test. The results showed that triazole 7 had the best antimicrobial activity against Bacillus cereus. In the chemical stimulus test, triazoles 6 and 7 were the most active compounds whereas in the hot‐plate test thiadiazoles 9 and 10 exhibited the highest analgesic activity. 相似文献
106.
In the last few years, the concepts of stability and Clifford regularity have been fruitfully extended by using star operations. In this article we deepen the study of star stable and star regular domains and relate these two classes of domains to each other. 相似文献
107.
Let M k (F) be the algebra of k ×k matrices over a field F of characteristic 0. If G is any group, we endow M k (F) with the elementary grading induced by the k-tuple (1,...,1,g) where g?∈?G, g 2?≠?1. Then the graded identities of M k (F) depending only on variables of homogeneous degree g and g ???1 are obtained by a natural translation of the identities of bilinear mappings (see Bahturin and Drensky, Linear Algebra Appl 369:95–112, 2003). Here we study such identities by means of the representation theory of the symmetric group. We act with two copies of the symmetric group on a space of multilinear graded polynomials of homogeneous degree g and g ???1 and we find an explicit decomposition of the corresponding graded cocharacter into irreducibles. 相似文献
108.
109.
Luca Scrivano Ortensia Ilaria Parisi Domenico Iacopetta Mariarosa Ruffo Jessica Ceramella Maria Stefania Sinicropi Francesco Puoci 《先进技术聚合物》2019,30(3):743-748
The present work reports on the synthesis of a molecularly imprinted polymer (MIP) based on methacrylic acid and ethylene glycol dimethacrylate for sunitinib delivery. Sunitinib (SUT) is a tyrosine kinase inhibitor used in many cancer diseases. Like the majority of the anticancer drugs, SUT suffers of a low bioavailability, and at the same time, it is characterized by a narrow therapeutic window. In order to reduce drug systemic toxicity, we synthesized a MIP‐based drug delivery system for SUT‐controlled release. MIP was obtained by bulk polymerization through the so‐called noncovalent approach. Rebinding experiments were performed to evaluate the success of the imprinting process and the ability of MIP to bind in a specific and selective fashion the template molecule. Resulting data showed that sunitinib rebinding percentage was 70%, while nonimprinted polymer (NIP) rebinding percentage was 46%. A not significant difference was observed between MIP and NIP in semaxanib binding experiments. Moreover, the drug release profiles were studied for both MIP and NIP. A sustained release was observed from sunitinib‐loaded MIP during 24 hours, reaching 58% after 6 hours and 76% at the end‐point. NIP, on the contrary, released almost 90% of the loaded drug within 6 hours. Furthermore, the drug carrier was tested in vitro against MCF‐7 cells, in which the cytotoxic effect of sunitinib released from MIP reached the maximum after 72 hours, while NIP completed its effect within 48 hours. These results demonstrated that molecularly imprinted polymers are suitable systems for SUT release. 相似文献
110.
Stefano Federico Tuhina Khan Nicola Relitti Giulia Chemi Margherita Brindisi Simone Brogi Ettore Novellino Daniela M. Zisterer Giuseppe Campiani Sandra Gemma Stefania Butini 《Tetrahedron letters》2018,59(51):4466-4470
We developed a Jocic-type protocol for the construction of the pyrrolonaphthoxazepine (PNOX) core. After an initial investigation based on the isolation of a trichloromethyl carbinol derivative, we shifted our attention towards a multicomponent single-step protocol. Screening of a variety of bases and solvents led to the identification of the optimum conditions for the preparation of the key α-aryloxy carboxylic acids to undergo intramolecular cyclization. The novel chemical route significantly improved overall yields for the preparation of PNOX-based compounds and was successfully extended to the preparation of 1,4-benzoxazinone-based templates. 相似文献