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991.
The regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone provided a new efficient synthetic route to joubertinamine (9.6% total yield over 10 steps). 相似文献
992.
Bruce S. Dien Nick Nagle Kevin B. Hicks Vijay Singh Robert A. Moreau Melvin P. Tucker Nancy N. Nichols David B. Johnston Michael A. Cotta Quang Nguyen Rodney J. Bothast 《Applied biochemistry and biotechnology》2004,115(1-3):937-949
Approximately 9% of the 9.7 billion bushels of corn harvested in the United States was used for fuel ethanol production in 2002, half of which was prepared for fermentation by dry grinding. The University of Illinois has developed a modified dry grind process that allows recovery of the fiber fractions prior to fermentation. We report here on conversion of this fiber (Quick Fiber [QF]) to ethanol. QF was analyzed and found to contain 32%wt glucans and 65%wt total carbohydrates. QF was pretreated with dilute acid and converted into ethanol using either ethanologenic Escherichia coli strain FBR5 or Saccharomyces cerevisiae. For the bacterial fermentation the liquid fraction was fermented, and for the yeast fermentation both liquid and solids were fermented. For the bacterial fermentation, the final ethanol concentration was 30 g/L, a yield of 0.44 g ethanol/g of sugar(s) initially present in the hydrolysate, which is 85% of the theoretical yield. The ethanol yield with yeast was 0.096 gal/bu of processed corn assuming a QF yield of 3.04 lb/bu. The residuals from the fermentations were also evaluated as a source of corn fiber oil, which has value as a nutraceutical. Corn fiber oil yields were 8.28%wt for solids recovered following prtetreatment. 相似文献
993.
In this work, we present a general scheme to improve quantum state transfer (QST) by taking advantage of quantum partially collapsing measurements. The scheme consists of a weak measurement performed at the initial time on the qubit encoding the state of concern and a subsequent quantum reversal measurement at a desired time on the destined qubit. We determine the strength qr of the post quantum reversal measurement as a function of the strength p of the prior weak measurement and the evolution time t so that near-perfect QST can be achieved by choosing p close enough to 1, with a finite success probability, regardless of the evolution time and the distance over which the QST takes place. The merit of our scheme is twofold: it not only improves QST, but also suppresses the energy dissipation, if any. 相似文献
994.
Shi W Petersen EB Nguyen DT Yao Z Chavez-Pirson A Peyghambarian N Yu J 《Optics letters》2011,36(18):3575-3577
We report a unique all fiber-based single-frequency Q-switched laser in a monolithic master oscillator power amplifier configuration at ~1920 nm by using highly Tm-doped germanate fibers for the first time. The actively Q-switched fiber laser seed was achieved by using a piezo to press the fiber in the fiber Bragg grating cavity and modulate the fiber birefringence, enabling Q-switching with pulse width and repetition rate tunability. A single-mode polarization maintaining large core 25 μm highly Tm-doped germanate fiber was used in the power amplifier stage. For 80 ns pulses with 20 kHz repetition rate, we achieved 220 μJ pulse energy, which corresponds to a peak power of 2.75 kW with transform-limited linewidth. 相似文献
995.
A systematic study of the upper semicontinuity and the lower semicontinuity of the solution map in parametric affine variational
inequalities is given in this paper. Several examples are constructed to analyze the results.
This work was supported by Korea Research Foundation Grant (KRF 2001-015-DP0049), the APEC Postdoctoral Fellowships Program,
and the KOSEF Brain Pool Program. 相似文献
996.
In this paper, we establish some new characterizations of metric regularity of implicit multifunctions in complete metric spaces by using lower semicontinuous envelopes of the distance functions to set-valued mappings. Through these new characterizations it is possible to investigate implicit multifunction theorems based on coderivatives and on contingent derivatives as well as the perturbation stability of implicit multifunctions. 相似文献
997.
In this paper, we study smooth metric measure space (M, g, e ?f dv) satisfying a weighted Poincaré inequality and establish a rigidity theorem for such a space under a suitable Bakry–Émery curvature lower bound. We also consider the space of f-harmonic functions with finite energy and prove a structure theorem. 相似文献
998.
Syntheses,Crystal Structures,and Properties of the Isotypic Pair [Cr(H2O)6]2[B12H12]3·15H2O and [In(H2O)6]2[B12H12]3·15H2O 下载免费PDF全文
Single crystals of [Cr(H2O)6]2[B12H12]3 · 15H2O and [In(H2O)6]2[B12H12]3 · 15H2O were obtained by reactions of aqueous solutions of the acid (H3O)2[B12H12] with chromium(III) hydroxide and indium metal shot, respectively. The title compounds crystallize isotypically in the trigonal system with space group R$\bar{3}$ c (a = 1157.62(3), c = 6730.48(9) pm for the chromium, a = 1171.71(3), c = 6740.04(9) pm for the indium compound, Z = 6). The arrangement of the quasi‐icosahedral [B12H12]2– dianions can be considered as stacking of two times nine layers with the sequence …ABCCABBCA… and the metal trications arrange in a cubic closest packed …abc… stacking sequence. The metal trications are octahedrally coordinated by six water molecules of hydration, while another fifteen H2O molecules fill up the structures as zeolitic crystal water or second‐sphere hydrating species. Between these free and the metal‐bonded water molecules, bridging hydrogen bonds are found. Furthermore, there is also evidence of hydrogen bonding between the anionic [B12H12]2– clusters and the free zeolitic water molecules according to B–Hδ– ··· δ+H–O interactions. Vibrational spectroscopy studies prove the presence of these hydrogen bonds and also show slight distortions of the dodecahydro‐closo‐dodecaborate anions from their ideal icosahedral symmetry (Ih). Thermal decomposition studies for the example of [Cr(H2O)6]2[B12H12]3 · 15H2O gave no hints for just a simple multi‐stepwise dehydration process. 相似文献
999.
Dinh Quang Khieu Duong Tuan Quang Tran Dai Lam Nguyen Huu Phu Jae Hong Lee Jong Seung Kim 《Journal of inclusion phenomena and macrocyclic chemistry》2009,64(1-2):73-81
Raman spectroscopy has been successfully employed in order to investigate the formation of β-cyclodextrin host–guest inclusion molecular complexes with several different azo-dye structures. The Raman pattern of the carbohydrate framework results negligible when neared to the magnificent intensity of the highly polarisable guest systems and a complete and feasible comparison of the spectral features between the free and the complexed situation of the guest molecule is allowed. In general, with respect to the free guest state, it was found within the complex that a hampering of Raman intensity displays, accompanied by a levelling directed variation of the relative peak intensities, and peculiar Raman peak broadening with shifts occur, relatable to the host–guest settling of inclusive intermolecular interactions. Supportively to the other commonly established characterising methods, or in valid alternative, Raman technique has proved astoundingly useful under the perspective of the diagnostic evaluation of cyclodextrin host–guest molecular inclusion for azo-dyes and, more generally, for a highly polarisable guest structure. It features sample non-destructivity, handiness, fastness and sensitive reproducibility, occasionally providing useful suggestions about the complexation topology. 相似文献
1000.
Thao T. P. Nguyen Dr. Foad Raji Dr. Cuong V. Nguyen Dr. Ngoc N. Nguyen Prof. Anh V. Nguyen 《Chemphyschem》2023,24(23):e202300062
Surfactants are used to control the macroscopic properties of the air-water interface. However, the link between the surfactant molecular structure and the macroscopic properties remains unclear. Using sum-frequency generation spectroscopy and molecular dynamics simulations, two ionic surfactants (dodecyl trimethylammonium bromide, DTAB, and sodium dodecyl sulphate, SDS) with the same carbon chain lengths and charge magnitude (but different signs) of head groups interact and reorient interfacial water molecules differently. DTAB forms a thicker but sparser interfacial layer than SDS. It is due to the deep penetration into the adsorption zone of Br− counterions compared to smaller Na+ ones, and also due to the flip-flop orientation of water molecules. SDS alters two distinctive interfacial water layers into a layer where H+ points to the air, forming strong hydrogen bonding with the sulphate headgroup. In contrast, only weaker dipole-dipole interactions with the DTAB headgroup are formed as they reorient water molecules with H+ point down to the aqueous phase. Hence, with more molecules adsorbed at the interface, SDS builds up a higher interfacial pressure than DTAB, producing lower surface tension and higher foam stability at a similar bulk concentration. Our findings offer improved knowledge for understanding various processes in the industry and nature. 相似文献