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11.
The reaction of ozone and gaseous platinum hexafluoride led to O2PtF6(s) and not the desired O3PtF6(s). Suggestions as to why the synthesis of O3PtF6(s) failed are made in terms of the known chemistry of the gaseous O
3
+
cation with O
+
5
proposed as an intermediate. 相似文献
12.
A program development methodology based on verified program transformations is described and illustrated through derivations of a high level bisimulation algorithm and an improved minimum-state DFA algorithm. Certain doubts that were raised about the correctness of an initial paper-and-pencil derivation of the DFA minimization algorithm were laid to rest by machine-checked formal proofs of the most difficult derivational steps. Although the protracted labor involved in designing and checking these proofs was almost overwhelming, the expense was somewhat offset by a successful reuse of major portions of these proofs. In particular, the DFA minimization algorithm is obtained by specializing and then extending the last step in the derivation of the high level bisimulation algorithm. Our experience suggests that a major focus of future research should be aimed towards improving the technology of machine checkable proofs — their construction, presentation, and reuse. This paper demonstrates the importance of such a technology to the verification of programs and program transformations. We believe that the utility of transformational systems to program development will ultimately rest on a practical program correctness technology. © 1996 John Wiley & Sons, Inc. 相似文献
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Crawley ML Goljer I Jenkins DJ Mehlmann JF Nogle L Dooley R Mahaney PE 《Organic letters》2006,8(25):5837-5840
The first efficient and regioselective palladium-catalyzed cyclization of internal alkynes and 2-amino-3-iodoacrylates to give moderate to excellent yields of highly functionalized pyrroles has been developed. This approach is applicable to a range of alkynes and affords the deacylated pyrrole under reaction conditions for most substrates. [reaction: see text] 相似文献
18.
Recent research has focused on increasing the evidentiary value of latent fingerprints through chemical analysis. Although researchers have optimized the use of organic and metal matrices for matrix‐assisted laser desorption/ionization‐mass spectrometry imaging (MALDI‐MSI) of latent fingerprints, the use of development powders as matrices has not been fully investigated. Carbon forensic powder (CFP), a common nonporous development technique, was shown to be an efficient one‐step matrix; however, a high‐resolution mass spectrometer was required in the low mass range due to carbon clusters. Titanium oxide (TiO2) is another commonly used development powder, especially for dark nonporous surfaces. Here, forensic TiO2 powder is utilized as a single‐step development and matrix technique for chemical imaging of latent fingerprints without the requirement of a high‐resolution mass spectrometer. All studied compounds were successfully detected when TiO2 was used as the matrix in positive mode, although, generally, the overall ion signals were lower than the previously studied CFP. TiO2 provided quality mass spectrometry (MS) images of endogenous and exogenous latent fingerprint compounds. The subsequent addition of traditional matrices on top of the TiO2 powder was ineffective for universal detection of latent fingerprint compounds. Forensic TiO2 development powder works as an efficient single‐step development and matrix technique for MALDI‐MSI analysis of latent fingerprints in positive mode and does not require a high‐resolution mass spectrometer for analysis. 相似文献
19.
Dr. A. F. Eftaiha Dr. Abdussalam K. Qaroush Ghada G. Kayed Abdel Rahman K. Abdel Rahman Dr. Khaleel I. Assaf Prof. Dr. Matthew F. Paige 《Chemphyschem》2020,21(16):1858-1865
A series of water soluble, surface-active ionic liquids (SAILs), namely, 1-alkyl-3-methyl imidazolium chlorides ([Cn-mim]Cl) and their mixtures with palmitic acid (PA) are investigated in Langmuir monolayers and Langmuir–Blodgett films. It is inferred from the surface pressure-area isotherms that C16-mim-IL mixes non-ideally with PA and stabilizes the binary mixed films. In addition, the residence of mim-IL at the water surface is enhanced as a function of the increasing alkyl side chain length. Generally, the compressional moduli values decrease upon increasing the content of the mim-ILs over a wide range of compositions. Furthermore, film relaxation measurements indicate that the IL component is selectively excluded from the mixed films upon achieving a certain target pressure. Brewster angle microscope images demonstrate minimal changes on the PA domains in the presence of either C4- and C8-mim-ILs, whereas presence of the hexadecyl counterpart results in the formation of condensed sheets. Atomic force microscopy imaging of deposited films show the formation of propeller-like aggregates when C8- or C16-mim-IL is present in the mixed films. 相似文献
20.
Hall WP Anker JN Lin Y Modica J Mrksich M Van Duyne RP 《Journal of the American Chemical Society》2008,130(18):5836-5837
A plasmonic switch based on the calcium-induced conformational changes of calmodulin is shown to exhibit reversible wavelength modulations in response to changing calcium concentration. The extinction maximum (lambdamax) of a localized surface plasmon resonance (LSPR) sensor functionalized with a novel calmodulin construct, cutinase-calmodulin-cutinase (CutCaMCut), reversibly shifts by 2-3 nm. A high-resolution (HR) LSPR spectrometer with a wavelength resolution (3sigma) of 1.5 x 10-2 nm was developed to detect these wavelength modulations in real-time, providing information about the dynamics and structure of the protein. The rate of conversion from open (Ca2+-bound) to closed (Ca2+-free) calmodulin is shown to be 4-fold faster than the reverse process, with a closing rate of 0.127 s-1 and opening rate of 0.034 s-1. As far as we are aware, this plasmonic switch marks the first use of LSPR spectroscopy to detect reversible conformational changes in an unlabeled protein. 相似文献