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Dr. Lidia A. Maslovskaya Dr. Andrei I. Savchenko Prof. Elizabeth H. Krenske Dr. Sharon Chow Tina Holt Dr. Victoria A. Gordon Dr. Paul W. Reddell Carly J. Pierce Prof. Peter G. Parsons Prof. Glen M. Boyle Prof. Andrei G. Kutateladze Prof. Craig M. Williams 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(51):11862-11867
Structurally unique halimanes EBC-232 and EBC-323, isolated from the Australian rainforest plant Croton insularis, proved considerably difficult to elucidate. The two diastereomers, which consist an unusual oxo-6,7-spiro ring system fused to a dihydrofuran, were solved by unification and consultation of five in silico NMR elucidation and prediction methods [i.e., ACDLabs, olefin strain energy (OSE), DP4, DU8+ and TD DFT CD]. Structure elucidation challenges of this nature are prime test case examples for empowering future AI learning in structure elucidation. 相似文献
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In this paper we give sufficient conditions that guarantee the mean curvature flow with free boundary on a pinched cylinder develops a Type 2 curvature singularity. We additionally prove that Type 0 singularities may only occur at infinity. 相似文献
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Upper and lower bounds are derived for the shear stress as it is determined by Saint-Venant's theory of flexure, and used to establish the asymptotic character of the classical Strength of Materials formula in the limit of vanishing thickness.
Résumé On dérive des limites supérieures et inférieures des contraintes tangentielles suivant la théorie de la flexion de Saint-Venant, que l'on utilise aux fins d'établir le caractère asymptotique de la formule de la Résistance des Matériaux dans le cas limite d'une épaisseur extrêmement petite.相似文献
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A convergent numerical method for modeling in situ biorestoration of contaminated groundwater is outlined. This method treats systems of transport-biodegradation equations by operator splitting in time. Transport is approximated by a finite element modified method of characteristics. The biodegradation terms are split from the transport terms and treated as a system of ordinary differential equations. Numerical results for vertical cross-sectional flow are presented. The effects of variable hydraulic conductivity and variable linear adsorption are studied. 相似文献
6.
The Newtonian potential is used to solve an inverse problem in which we seek the shape of an inhomogeneity in an infinite elastic matrix under uniform applied stresses at infinity such that certain stress components are uniform on the boundary of the inhomogeneity. It is shown that ellipsoids furnish the solution of this inverse problem. Exact and general expressions for the stress and displacement are given explicitly for points in the elastic matrix outside the inhomogeneity. The solution of the corresponding plane deformation problem is found as a limiting case. Several applications are presented, and results from the literature are confirmed as special cases. 相似文献
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Enhancing the Value of Free Metals in the Synthesis of Lanthanoid Formamidinates: Is a Co‐oxidant Needed? 下载免费PDF全文
Prof. Dr. Glen B. Deacon Prof. Dr. Peter C. Junk Dr. Daniel Werner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(1):160-173
Treatment of N,N′‐bis(aryl)formamidines (ArFormH), N,N′‐bis(2,6‐difluorophenyl)formamidine (DFFormH) or N,N′‐bis(2,6‐diisopropylphenyl)formamidine (DippFormH), with europium metal in CH3CN is an efficient synthesis of the divalent complexes: [{Eu(DFForm)2(CH3CN)2}2] ( Eu1 ) or [Eu(DippForm)2(CH3CN)4] ( Eu2 ). The synthetic method was extended to ytterbium, but the metal required activation by addition of Hg0. With DFFormH in CH3CN, [{Yb(DFForm)2(CH3CN)}2] ( Yb1 ) was obtained in good yield, and [Yb(DFForm)2(thf)3] ( Yb3 ) was obtained from a synthesis in CH3CN/THF. Thus, this synthetic method completely circumvents the use of either salt metathesis, or redox transmetallation/protolysis (RTP) protocols to prepare divalent rare‐earth formamidinates. Heating Yb1 in PhMe/C6D6 resulted in decomposition to trivalent products, including one from a CH3CN activation process. For a synthetic comparison, divalent ytterbium DFForm and DippForm complexes were synthesised by RTP reactions between Yb0, Hg(R)2 (R=Ph, C6F5), and ArFormH in THF, leading to the isolation of either [Yb(DFForm)2(thf)3] ( Yb3 ), or the first five coordinate rare‐earth formamidinate complex [Yb(DippForm)2(thf)] ( Yb4 b ), and, from adjustment of the stoichiometry, trivalent [Yb(DFForm)3(thf)] ( Yb6 ). Oxidation of Yb3 with benzophenone (bp), or halogenating agents (TiCl4(thf)2, Ph3CCl, C2Cl6) gave [Yb(DFForm)3(bp)] or [Yb(DFForm)2Cl(thf)2], respectively. Furthermore, the structural chemistry of divalent ArForm complexes has been substantially broadened. Not only have the highest and lowest coordination numbers for divalent rare‐earth ArForm complexes been achieved in Eu2 and Yb4 b , respectively, but also dimeric Eu1 and Yb1 have highly unusual ArForm bridging coordination modes, either perpendicular μ‐1κ(N:N′):2κ(N:N′) in Eu1 , or the twisted μ‐1κ(N:N′):2κ(N′:F′) DFForm coordination in Yb1 , both unprecedented in divalent rare‐earth ArForm chemistry and in the wider divalent rare‐earth amidinate field. 相似文献
10.
Pingli Lv Rongxiu Zhu Tongxiang Lu Steven E. Wheeler Dongju Zhang Ruoxi Wang Chengbu Liu 《Tetrahedron: Asymmetry》2013,24(24):1598-1604
Computational studies to determine the origin of enantioselectivity in the (1R,2R)-1,2-diphenylethane-1,2-diamine (DEPN)–Brønsted acid catalyzed epoxidation of 2-cyclohexen-1-one have been performed using density functional theory. Transition states for conjugate addition and ring closure steps of the epoxidations catalyzed by three different catalyst systems were characterized. Our calculations show that the Csp2H?O H-bond interaction between the benzene ring of the catalyst and H2O is mainly responsible for the chiral discrimination observed. The Brønsted acid counterion plays a very important role in ensuring high enantioselectivity by improving the rigidity of the transition state structures to allow the efficient formation of the Csp2H?O H-bond. Moreover, we explain why these two diamine catalysts (1S,2S)-DACH and (1R,2R)-DPEN display consistent enantioselectivities in the catalytic epoxidation of 2-cyclohexen-1-one when combining with three different cocatalysts; achiral TFA, and chiral (R)- and (S)-TRIP. 相似文献