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41.
Harrison S. Ewan Christine S. Muli Steven Touba Amy T. Bellinghiere Anne M. Veitschegger Travis B. Smith William L. Pistel II William T. Jewell Rebecca K. Rowe John P. Hagen Hasan Palandoken 《Tetrahedron letters》2014
A straightforward synthesis of a novel class of sugar surfactants is described. The key step is the chemoselective condensation of a hydrophobic alkoxyamine with the resident aldehyde/ketone moiety on a hydrophilic sugar. Neither protection/deprotection of the sugars nor extensive product purification is required. The method allows for the facile adjustment of hydrophobic and hydrophilic domains of the sugar oxime ether surfactant and uses inexpensive, readily accessible, and renewable materials. 相似文献
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Kuzhikalail M. Abraham Rebecca Schiff 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):177-181
Abstract Some reactions of the aliphatic amides, CH3CONH2, CH3CONHCH3, CH3CON(CH3)2 and CH3CON(C2H5)2 with elemental S and sodium sulfides, Na2S n , n ≥ 1, have been studied. The initial reaction product with elemental sulfur appears to be a substituted polysulfane, CH3COS n NR, formed by the insertion of the sulfur chain into the C[sbnd]N bond. This product decomposes on further heating, forming COS as the major gas product. In solutions of Na2S n in the amides, the reactive material appears to be elemental S, present in equilibrium with S n ?2. In the N-dialkyl substituted amides, CH3CON(CH3)2 and CH3CON(C2H5)2, the tetrasulfide is uniquely stabilized by solvent coordination so that solutions of Na2S4 in these amides are stable for long periods of time at 130°C. 相似文献
44.
We report the synthesis of three new dipyrrinone imine analogues and the characterisation of their self-association properties. Based on vapour pressure osmometry and nuclear magnetic resonance studies, placing the imine functional group at C(9) of the dipyrrinone disrupts the native self-association of the dipyrrinone core in a manner that correlates with the conformational A-value of the imine N-substituent. 相似文献
45.
Mirko Aden Andreas Roesner Alexander Olowinsky 《Journal of Polymer Science.Polymer Physics》2010,48(4):451-455
In laser transmission welding of thermoplastics the optical properties of the joining parts determine the quality of the welding result. Especially, the scattering of laser radiation in the transparent welding part has an impact on weld seam properties. This scattering is caused by additives. For polycarbonate (PC) with different additives the transmittance, the reflectance and the collimated transmittance are measured with a UV‐VIS‐NIR spectrometer. From this data, the optical properties, such as scattering coefficient, absorption coefficient, and anisotropy factor are calculated. The calculations are made with the aid of the four‐flux model of radiation transport in the diffusive approximation. The results show that the additives have a significant influence on the scattering coefficient. For most additives under consideration the scattering is forward directed, which means that most of the radiation is transmitted into the absorbing welding part. However, the power density distribution of the transmitted radiation may differ significantly from PC without additives. So, the weld seam may also differ due to different additives. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 451–455, 2010 相似文献
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Rebecca Waldecker 《Archiv der Mathematik》2011,97(1):11-16
This note is concerned with a particular kind of primitive pairs in finite groups. Applications of the results that are proved
here play a key role in the author’s work towards a new proof of Glauberman’s Z*-Theorem. 相似文献
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Dmytro Neshchadin Dr. Rebecca Levinn Georg Gescheidt Prof. Dr. Stephen N. Batchelor Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(23):7008-7016
Polyphenols occur naturally in a vast variety of plants. One of their predominant properties is their antioxidant activity. To provide a deeper understanding of the antioxidant mechanism, 1H CIDNP spectroscopy (CIDNP=chemically induced dynamic nuclear polarization) is used to study model hydrogen abstraction reactions with four catechin‐based polyphenols: catechin (CA), gallocatechin (GC), epigallocatechin (EGC), and epigallocatechin gallate (EGCG). The experiments involve photoinduced hydrogen‐atom transfer to a hydrogen abstractor (e.g., excited isopropylthioxanthone) followed under steady‐state conditions and in a time‐resolved fashion (resolution 500 ns–1 ms). It is found that hydrogen abstraction is an essentially stochastic process with a slight preference for the B rings in the catechin‐based polyphenols. Remarkably, analogous reactivity patterns could be followed in the “real systems”, green tea and red wine. We also show that CIDNP can be used as a semiquantitative tool to assess chemical reactivity. 相似文献
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