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91.
We consider principal pivot transform (pivot) on graphs. We define a natural variant of this operation, called dual pivot, and show that both the kernel and the set of maximally applicable pivots of a graph are invariant under this operation. The result is motivated by and applicable to the theory of gene assembly in ciliates. 相似文献
92.
Oluseye K. Onajole Patrick Govender Thavendran Govender Glenn E. M. Maguire Hendrik G. Kruger 《Structural chemistry》2010,21(6):1203-1209
The NMR elucidation of five novel SQ109 analogues including SQ109 is reported herein. These derivatives were synthesized as
potential anti-tuberculosis candidates. One-dimensional NMR (1H and 13C) techniques show a series of overlapping signals from the methine and methylene groups of these compounds, thereby making
it extremely difficult to assign all NMR signals. Two-dimensional (2D) NMR techniques were instrumental in overcoming these
challenges. This paper appears to be a rare report on the complete structure elucidation of mono-substituted adamantane moieties. 相似文献
93.
Oluseye K. Onajole Maya M. Makatini Patrick Govender Thavendran Govender Glenn E. M. Maguire Hendrik G. Kruger 《Magnetic resonance in chemistry : MRC》2010,48(3):249-255
The synthesis and complete NMR elucidation of eight novel pentacycloundecane (PCU) derivatives are reported. These compounds are precursors in the synthesis of PCU‐based anti‐tuberculosis (TB) agents and potential human immunodeficiency virus (HIV) protease inhibitors. Two‐dimensional (2D) NMR techniques were used to assign the NMR spectra for these compounds. Substitution of the cage molecule at (C‐8/11) further complicates the assignment, since some of the substituted alkyl chain groups overlap with the cage proton signals. The side chain heteroatoms also introduce a rare through‐space deshielding effect to some of the carbon atoms of the cage skeleton. Ring strain in the rigid cage skeleton appears to induce drastic electronic changes in some parts of the cage framework. This observation is more dramatic for the C‐4 methylene group of the cage diols and the cage ethers. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
94.
We investigate the derived structures of compact polygons at half-regular and at regular points. This enables us to give a geometric characterization of the real or complex split Cayley hexagon. 相似文献
95.
Hendrik De Bie 《Physics letters. A》2008,372(24):4350-4352
A superspace version of the Schrödinger equation with a delta potential is studied using Fourier analysis. An explicit expression for the energy of the single bound state is found as a function of the super-dimension M in case M is smaller than or equal to 1. In the case when there is one commuting and 2n anti-commuting variables also the wave function is given explicitly. 相似文献
96.
In this paper, we prove that the Hermitian quadrangle is the unique generalized quadrangle Γ of order (q
2, q
3) containing some subquadrangle of order (q
2, q) isomorphic to such that every central elation of the subquadrangle is induced by a collineation of Γ.
Dedicated to Dan Hughes on the occasion of his 80th birthday. 相似文献
97.
Ultraviolet Absorption Induces Hydrogen‐Atom Transfer in G⋅C Watson–Crick DNA Base Pairs in Solution
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Dr. Katharina Röttger Hugo J. B. Marroux Dr. Michael P. Grubb Philip M. Coulter Hendrik Böhnke Dr. Alexander S. Henderson Dr. M. Carmen Galan Prof. Friedrich Temps Prof. Andrew J. Orr‐Ewing Dr. Gareth M. Roberts 《Angewandte Chemie (International ed. in English)》2015,54(49):14719-14722
Ultrafast deactivation pathways bestow photostability on nucleobases and hence preserve the structural integrity of DNA following absorption of ultraviolet (UV) radiation. One controversial recovery mechanism proposed to account for this photostability involves electron‐driven proton transfer (EDPT) in Watson–Crick base pairs. The first direct observation is reported of the EDPT process after UV excitation of individual guanine–cytosine (G?C) Watson–Crick base pairs by ultrafast time‐resolved UV/visible and mid‐infrared spectroscopy. The formation of an intermediate biradical species (G[?H]?C[+H]) with a lifetime of 2.9 ps was tracked. The majority of these biradicals return to the original G?C Watson–Crick pairs, but up to 10 % of the initially excited molecules instead form a stable photoproduct G*?C* that has undergone double hydrogen‐atom transfer. The observation of these sequential EDPT mechanisms across intermolecular hydrogen bonds confirms an important and long debated pathway for the deactivation of photoexcited base pairs, with possible implications for the UV photochemistry of DNA. 相似文献
98.
99.
100.
Denis?Constales Hendrik?De Bie Pan?LianEmail author 《Journal of Fourier Analysis and Applications》2017,23(2):462-483
In this paper, we develop a new method based on the Laplace transform to study the Clifford-Fourier transform. First, the kernel of the Clifford-Fourier transform in the Laplace domain is obtained. When the dimension is even, the inverse Laplace transform may be computed and we obtain the explicit expression for the kernel as a finite sum of Bessel functions. We equally obtain the plane wave decomposition and find new integral representations for the kernel in all dimensions. Finally we define and compute the formal generating function for the even dimensional kernels. 相似文献