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751.
752.
Site-specific 13C labeling offers a desirable means of eliminating unwanted relaxation pathways and coherent magnetization transfer in NMR relaxation experiments. Here we use [1-13C]-glucose as the sole carbon source in the growth media for protein overexpression in Escherichia coli. The approach results in specific incorporation of 13C at isolated positions in the side chains of aromatic amino acids, which greatly simplifies the measurements and interpretation of 13C relaxation rates in these spin systems. The method is well suited for characterization of chemical exchange by CPMG or spin-lock relaxation methods. We validated the method by acquiring 13C rotating-frame relaxation dispersion data on the E140Q mutant of the C-terminal domain of calmodulin, which reveal conformational exchange dynamics with a time constant of 71 mus for Y138. 相似文献
753.
Salem MY El-Guindi NM Mikael HK Abd-El-Fattah Lel-S 《Chemical & pharmaceutical bulletin》2006,54(12):1625-1632
Two stability-indicating methods, namely densitometric TLC and derivative spectrophotometry for the determination of the fluoroquinolone antibacterials lomefloxacin (Lfx), moxifloxacin (Mfx), and sparfloxacin (Sfx) in the presence of their acid degrades are described. Acid degradation was adopted and the main decarboxylated product separated by TLC. Degradation products were identified confirming a previously mentioned degradation scheme. The densitometric method is based on the separation of the intact drug from its acid degradation product on silica gel G plates using different mobile phases and the spots of the intact drugs were scanned at 288, 290, and 292 nm for Lfx, Mfx, and Sfx, respectively. The derivative spectrophotometric method utilizes first derivative D(1) UV spectrophotometry with zero crossing points at 295.2 nm for Lfx, 280.4 and 303.4 nm for Mfx, and 280.8 nm for Sfx. Regression analysis of Beer's plots showed good correlation in the concentration ranges 0.2-1.2, 0.1-1.4, and 0.5-2.0 microg/spot for Lfx, Mfx, and Sfx, respectively, in the densitometric method and 2-16 microg/ml for all drugs in the derivative spectrophotometric method. The proposed methods were successfully applied for the determination of the investigated drugs in bulk powder with mean percentage accuracy ranges from 98.93 to 101.25% for the TLC method and from 98.18 to 100.35% for the D(1) method. The proposed methods were also applied for the determination of the investigated drugs in their pharmaceutical dosage forms and their validity was assessed using the standard addition technique with mean percentage recovery ranging from 100.25 to 101.70% in the TLC method and from 99.27 to 102.12% in the D(1) method. The selectivity of the proposed methods was tested by the analysis of laboratory-prepared mixtures containing different percentages of the studied drugs and their acid degrades. The proposed methods were found selective for the determination of the intact drugs in the presence of up to 90% of their degrades in the TLC method and 70% for Lfx and 90% for Mfx and Sfx in the D(1) method. 相似文献
754.
Jönsson S Uusitalo T van Bavel B Gustafsson IB Lindström G 《Journal of chromatography. A》2006,1111(1):71-75
A gas chromatography-high-resolution mass spectrometry (GC-HRMS) method using solid-phase microextraction (SPME) for the determination of 2,4,6-trichloroanisole (TCA) and 2,4,6-tribromoanisole (TBA) in wine at low ng L(-1) levels was developed. A robust SPME method was developed by optimizing several different parameters, including type of fiber, salt addition, sample volume, extraction and desorption time. The quantification limit for TCA and TBA in wine was lowered substantially using GC-HRMS in combination with the optimized SPME method and allowed the detection of low analyte concentrations (ng L(-1)) with good accuracy. Limits of quantification for red wine of 0.3 ng L(-1) for TCA and 0.2 ng L(-1) for TBA with gas chromatography-negative chemical ionization mass spectrometry and 0.03 ng L(-1) for TCA and TBA were achieved using GC-HRMS. The method was applied to 30 wines of which 4 wines were sensorically qualified as cork defected. TCA was found in three of these wines with concentrations in the range 2-25 ng L(-1). TBA was not detected in any of the samples. 相似文献
755.
Lampinen-Salomonsson M Bondesson U Petersson C Hedeland M 《Rapid communications in mass spectrometry : RCM》2006,20(9):1429-1440
This paper describes a way of differentiating between the three isomers of estriol glucuronide by the use of chemical derivatization and liquid chromatography/electrospray tandem mass spectrometry (MS/MS). In their native form, these isomers gave rise to almost identical product ion spectra, involving the neutral loss of 176 Da (i.e. monodehydrated glucuronic acid), which made it impossible to determine the position of conjugation by MS/MS alone. In order to change the fragmentation pathways, positive charges were introduced into the analytes by chemical derivatization. The following reagents were tested: 2-chloro-1-methylpyridinium iodide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and 2-picolylamine. Interestingly, derivatization using a combination of all three reagents gave a selective fragmentation pattern that could differentiate between the isomers estriol-16-glucuronide and estriol-17-glucuronide. Estriol-3-glucuronide, which lacks a free phenolic group, could be differentiated through a different type of reaction product when exposed to 2-chloro-1-methylpyridinium iodide. Furthermore, in order to assist structural assignment of the fragments, their accurate masses were determined using a hybrid quadrupole time-of-flight mass spectrometer and fragmentation pathways were elucidated by the use of MS3 on an ion trap mass spectrometer. 相似文献
756.
Hynninen AP Panagiotopoulos AZ Rechtsman MC Stillinger FH Torquato S 《The Journal of chemical physics》2006,125(2):24505
We calculate the global phase diagram using classical statistical mechanics for an isotropic pair potential that has been previously [Rechtsman et al., Phys. Rev. Lett. 95, 228301 (2005)] shown to produce the low-coordinated two-dimensional honeycomb crystal as the ground-state structure. Low-coordinated crystals are of practical interest because they have desirable photonic band-gap properties. The phase diagram is obtained from Helmholtz free energies calculated using thermodynamic integration and Monte Carlo simulations. Our results show that the honeycomb crystal remains stable in the global phase diagram even after temperature effects are taken fully into account. Other stable phases in the phase diagram are high and low density triangular phases and a fluid phase. We find no evidence of gas-liquid or liquid-liquid phase coexistence. 相似文献
757.
758.
Lindén AA Johansson M Hermanns N Bäckvall JE 《The Journal of organic chemistry》2006,71(10):3849-3853
A new flavin catalyst 2 immobilized in an ionic liquid ([BMIm]PF6) was used for the highly selective oxidation of sulfides to sulfoxides by hydrogen peroxide. The sulfoxides were obtained in good to high yields and high selectivity without any detectable overoxidation to sulfone. The catalyst in the ionic liquid was recycled up to seven times without loss of activity or selectivity. 相似文献
759.
We prove a Strong Haagerup inequality with operator coefficients. If for an integer d, denotes the subspace of the von Neumann algebra of a free group FI spanned by the words of length d in the generators (but not their inverses), then we provide in this paper an explicit upper bound on the norm on , which improves and generalizes previous results by Kemp–Speicher (in the scalar case) and Buchholz and Parcet–Pisier (in the non-holomorphic setting). Namely the norm of an element of the form ∑i=(i1,…,id)aiλ(gi1gid) is less than , where M0,…,Md are d+1 different block-matrices naturally constructed from the family (ai)iId for each decomposition of IdIl×Id−l with l=0,…,d. It is also proved that the same inequality holds for the norms in the associated non-commutative Lp spaces when p is an even integer, pd and when the generators of the free group are more generally replaced by *-free -diagonal operators. In particular it applies to the case of free circular operators. We also get inequalities for the non-holomorphic case, with a rate of growth of order d+1 as for the classical Haagerup inequality. The proof is of combinatorial nature and is based on the definition and study of a symmetrization process for partitions. 相似文献
760.
Mikael Janvid 《Acta Analytica》2009,24(4):263-274
The notion of entitlement plays an important role in some influential epistemologies. Often the epistemological motive for
introducing the concept is to accommodate certain externalist intuitions within an internalist framework or, conversely, to
incorporate internalist traits into an otherwise externalist position. In this paper two prominent philosophers will be used
as examples: Tyler Burge as a representative of the first option and Fred Dretske as one of the second. However, even on the
assumption that the concept of entitlement is sufficiently clarified, accomplishing these results is easier said than done
– especially if we also want to ascribe positive epistemic value to entitlement. It will be shown that the epistemic value
of entitlement is either granted at the expense of the epistemic value of justification or the value ends up below the level
of value at which the epistemologists employing the concept of entitlement are aiming. 相似文献