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81.
Angurell I Martínez-Ruiz I Rossell O Seco M Gómez-Sal P Martin A 《Chemical communications (Cambridge, England)》2004,(15):1712-1713
Tri(N-pyrrolyl)phosphine reacted with the sigma/pi complex [Pd(mu-Cl)(COD-MeO)]2 to give the octa-cycle [Pd(mu-Cl)[P(pyrl)3]]8 containing four Pd(I)-Pd(I) unbridged bonds. 相似文献
82.
Madrigal B Puebla P Peláez R Caballero E Medarde M 《The Journal of organic chemistry》2003,68(3):854-864
The methodology for the synthesis of podophyllotoxin and thuriferic acid-type lignans has been applied to derivatives carrying a naphthalene moiety. Starting from the 1,3-dithiane of 2-naphthaldehyde afforded the expected analogues in the 2,1-naphthalene series. The preferred conformations of these compounds are influenced by the bulky naphthalene system. By contrast, 1,8-bridged products were obtained from the 1,3-dithiane of 1-naphthaldehyde. In this series, polycyclic naphthalene lignan analogues were isolated after deprotection and/or desulfurization reactions. The cyclizations produced in this process are due to the proximity between the 3,4,5-trimethoxyphenyl moiety and the reacting C-2 of the 1,3-dithiane ring. 相似文献
83.
Kleij AW Souto B Pastor CJ Prados P de Mendoza J 《The Journal of organic chemistry》2003,68(22):8711-8714
The selective preparation and complete structural characterization of a small series of 1,2-anti-heterodisubstituted calix[4]arenes has been accomplished. These compounds were obtained in two steps from unsubstituted p-tert-butylcalix[4]arene by tribenzoylation and a subsequent one-pot, two-step sequence involving alkylation with simultaneous partial deacylation, resulting in heterodisubstituted calixarenes carrying an alkyl and an aroyl group. The monoalkyl-tribenzoyl intermediate, prior to in situ deprotection, could also be isolated. 相似文献
84.
85.
We are interested in the maximum possible number of facets that Dirichlet stereohedra for three-dimensional crystallographic
groups can have. In two previous papers, D. Bochiş and the second author studied the problem for noncubic groups. This paper
deals with “full” cubic groups, while “quarter” cubic groups are left for a subsequent paper. Here, “full” and “quarter” refers
to the recent classification of three-dimensional crystallographic groups by Conway, Delgado-Friedrichs, Huson and Thurston.
This paper’s main result is that Dirichlet stereohedra for any of the 27 full groups cannot have more than 25 facets. We also
find stereohedra with 17 facets for one of these groups.
Research partially supported by the Spanish Ministry of Education and Science, grant number MTM2005-08618-C02-02. 相似文献
86.
Juan M. Antelo Florencio Arce Juan Crugeiras Julia Franco Pilar Rodriguez Angel Varela 《国际化学动力学杂志》1990,22(12):1271-1282
This article reports the kinetics of the decomposition of N-bromoserine formed rapidly by bromation of serine by BrO?. The main decomposition products are glycolaldehyde, ammonia, carbon dioxide, and bromide ions at pH < 11.5, and β-hydroxypyruvic acid, ammonia, and bromide ions at pH > 11.5. The reaction is of order one with respect to N-bromoserine, and is independent of ionic strength and excess serine. The rate constant increases with increasing pH at pH > 11 and with decreasing pH at pH < 8, and over the range pH 8–11 has the constant value 1.67 × 10?3 s?1 at 298 K. 相似文献
87.
In this paper we extend and generalize several known estimates for homogeneous polynomials and multilinear mappings on Banach spaces. Applying the theory of absolutely summing nonlinear mappings, we prove that estimates which are known for mappings on ?p spaces in fact hold true for mappings on arbitrary Banach spaces. 相似文献
88.
Pérez CM Rodríguez-Delgado A Palma P Álvarez E Gutiérrez-Puebla E Cámpora J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(46):13834-13842
Manganese alkyl complexes stabilised by 2,6-bis(N,N'-2,6-diisopropyl-phenyl)acetaldiminopyridine ((iPr)BIP) have been selectively prepared by reacting suitable alkylmanganese(II) precursors, such as homoleptic dialkyls [(MnR(2))(n)] or the corresponding THF adducts [{MnR(2)(thf)}(2)] with the mentioned ligand. For R=CH(2)CMe(2)Ph or CH(2)Ph, formally Mn(I) derivatives are produced, in which one of the two R groups migrates to the 4-position of the central pyridine ring in the (iPr)BIP ligand. In contrast, a true dialkyl complex [MnR(2)((iPr)BIP)] can be isolated for R=CH(2)SiMe(3). In solution, this compound slowly evolves to the corresponding Mn(I) monoalkyl derivative. A detailed study of this reaction provides insights on its mechanism, showing that it proceeds through successive alkyl migrations, followed by spontaneous dehydrogenation. Protonation of [Mn(CH(2)SiMe(3))(2)((iPr)BIP)] with the pyridinium salt [H(Py)(2)][BAr'(4)] (Ar'=3,5-C(6)H(3)(CF(3))(2)) leads to the cationic species [Mn(CH(2)SiMe(3))(Py)((iPr)BIP)](+). Alternatively, the same complex can be produced by reaction of the pyridine complex [{Mn(CH(2)SiMe(3))(2)(Py)}(2)] with the protonated ligand salt [H(iPr)BIP](+)[BAr'(4)](-). This last reaction allows the synthesis of analogous cationic alkylmanganese(II) derivatives, when precursors of type [MnR(2)((iPr)BIP)] are not available. Treatment of these neutral and cationic (iPr)BIP alkylmanganese derivatives with a range of typical co-catalysts (modified methylaluminoxane (MMAO), B(C(6)F(5))(3), trimethyl or triisobutylaluminum) does not lead to active ethylene polymerisation catalysts. 相似文献
89.
Joana Ferreira da Costa Franco Fernández Xerardo García-Mera Pilar Midón 《Tetrahedron》2010,66(34):6797-6805
Starting from readily available N-benzyl protected methyl 3,5-bis(hydroxymethyl)pirrolidinecarboxylate a number of racemic methyl t-3,t-5-disubstitutedprolinates have been synthesised, thus opening a practical way towards the preparation of a variety of putative proline-mimetics. In this context, N-Boc protected derivatives proved to be better intermediates than their N-benzyl counterparts in terms of cleanness and overall yield of the synthetic procedure. 相似文献
90.
Francisco J. Salgado Sara Vázquez Amparo Pérez-Díaz Pilar Arias 《Analytica chimica acta》2010,658(1):18-3648
Serum is a typical sample for non-invasive studies in clinical research. Its proteome characterization is challenging, since requires extensive protein depletion. Methods used nowadays for removal of high-abundance proteins are expensive or show quite often a low loading capacity, which has strong repercussions on the number of samples and replicates per analysis.In order to deplete immunoglobulins (Igs) and albumin (HSA) from 1 mL serum samples, we have developed a protocol based on a combination of thiophilic chromatography, not previously used in clinical proteomics, and a HSA-specific resin. Ig/HSA-depleted samples, immunoglobulinome and albuminone were analyzed by 2-DE. Thiophilic chromatography, coupled with HSA-depletion, allows a good 2-DE resolution as well as the visualization of new spots. Moreover, it yields enough protein to evaluate technical variability and facilitate subsequent protein identification. To validate the protocol, we carried out a preliminary comparative study between triplicate Igs/HSA-depleted serum samples from healthy control individuals and recently diagnosed/untreated rheumatoid arthritis (RA) patients. RA patients showed several acute phase proteins, as well as additional serum proteins, differentially and significantly regulated.Therefore, thiophilic chromatography can be used as an efficient and economical method in 2-DE to deplete immunoglobulins from large human serum samples before a more extensive fractioning. 相似文献