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排序方式: 共有606条查询结果,搜索用时 31 毫秒
61.
62.
Targeting the Two Oncogenic Functional Sites of the HPV E6 Oncoprotein with a High‐Affinity Bivalent Ligand
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63.
Balbina P. García-Aguilar Antonio Avalos Ramirez J. Peter Jones Michèle Heitz 《Chemical Papers》2011,65(3):373-379
The emissions of methane (CH4), a powerful greenhouse gas (GES), contribute to the increase in GES concentration level in the atmosphere. For this reason,
the importance of controlling CH4 emissions of anthropogenic origin has increased over the last decades. Physicochemical and biological processes are available
for treating CH4. For this reason, such properties as the solubility of CH4 in aqueous solutions and organic solvents are of great relevance in different applications in environmental engineering and
biotechnology. In this study, the solubility of CH4 was determined at 298 K and 101.3 kPa in organic solvents, such as polyoxyethylenesorbates (Tween 20, Tween 40, and Tween
60), and linear alcohols (methanol, ethanol, and butan-1-ol) alone and in their admixtures. Admixtures of methanol with butan-1-ol
exhibited the highest solubility of CH4, of around 0.49 g m−3 of solvent, whereas the solubility of CH4 in linear alcohols varied from 0.167 g m−3 to 0.41 g m−3 of solvent. In the case of Tweens, CH4 solubility decreased with the hydrophilic-lipophilic balance (HLB) number. 相似文献
64.
65.
Kim YA Ramirez DM Costain WJ Johnston LJ Bittman R 《Chemical communications (Cambridge, England)》2011,47(32):9236-9238
The bioactivity of natural, long-chain ceramides has until now been studied after its delivery to cells in organic solvent mixtures containing dodecane. We have synthesized ceramides conjugated to a (6-bromo-7-hydroxycoumarin-4-yl)methyl group. The photocaged ceramide is efficiently released with 350 nm light in aqueous solution at neutral pH, thus providing a promising new tool to study ceramide's properties. 相似文献
66.
67.
Woo-young So J. Magnus Wikberg Oleg Mitrofanov Theo Siegrist Arthur P. Ramirez 《Solid State Communications》2007,142(9):483-486
We report doping effects in an organic semiconductor, crystalline rubrene. Oxygen-related states are introduced (removed) by annealing in oxygen (vacuum), at an elevated temperature. Room temperature stability is found in the resulting effects: (1) about two orders of magnitude increase in carrier density at equilibrium, (2) significant modification of threshold voltages, and (3) an unchanged field-effect mobility in the on-current state. Density of states data are modeled as tunneling from the valence band in the channel region into deep-level acceptors in the adjacent region. These oxygen acceptors are the likely dopant species. 相似文献
68.
Virgil Percec Anatoliy V. Popov Ernesto Ramirez‐Castillo Oliver Weichold 《Journal of polymer science. Part A, Polymer chemistry》2003,41(21):3283-3299
The first example of living radical polymerization of vinyl chloride carried out in water at 25 °C is reported. This polymerization was initiated by iodoform and catalyzed by nascent Cu0 produced by the disproportionation of CuI in the presence of strongly CuII binding ligands such as tris(2‐aminoethyl)amine or polyethyleneimine. The resulting poly(vinyl chloride) was free of structural defects, had controlled molecular weight and narrow molecular weight distribution, contained two ~CHClI active chain ends, and had a higher syndiotacticity (62%) than the one obtained by conventional free‐radical polymerization at the same temperature (56%). This novel polymerization proceeds, most probably, by a combination of competitive pathways that involves activation by single electron transfer mediated by nascent Cu0 and degenerative chain transfer. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3283–3299, 2003 相似文献
69.
M. A. Mora Laura Galicia M. A. Mora‐Ramirez 《International journal of quantum chemistry》2004,97(6):983-991
The molecular and electronic structures of 5‐amino‐1,10‐phenanthroline and its monoprotonated and diprotonated species were obtained from ab initio quantum mechanical calculations with unrestricted Hartree–Fock (HF) and Møller–Plesset perturbation theories. The analysis of the net atomic charges and the total spin densities show three possible sites for the monomeric coupling in the polymerization process. The minimal energy conformation for the different kinds of coupling in the formation of the dimers was obtained. The studies were extended to the HF/6‐311 + G(2d,p)//B3LYP (Becke's three‐parameter exchange functional and the gradient‐corrected functional of Lee, Yang, and Paar)/6‐31G(d) level of theory to obtain theoretical nuclear magnetic resonance spectra to study the number and kinds of species involved in the protonation mechanism. Theoretical and experimental nuclear magnetic resonance spectra are in excellent agreement. © 2004 Wiley Periodicals, Inc. Int J Quantum Chem, 2004 相似文献
70.