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951.
We have measured, by means of ultrafast x‐ray absorption and optical spectroscopy, the M‐O (M=Fe, Co) and Co‐N metal to ligand bond length change as a function of time and the formation and decay of the excited states and intermediate species, after excitation with a 267 nm femtosecond pulse. These experimental data combined with DFT calculations allowed us to determine the mechanism of electron transfer operating in the redox reaction of two metal‐ligand complexes, [M(III)(C2O4)3]3‐ and [Co(III)(NH3)6 ]3+. Based on the data we find that, even though both molecules are excited into their charge transfer band, the redox reaction of [M(III)(C2O4)3]3‐ proceeds via intermolecular electron transfer while [Co(III)(NH3)6 ]3+ electron transfer mechanism is intramolecular. 相似文献
952.
Xue-Peng Liu Jie Feng Lu Zhang Qing-Tao Gong Jia-Yong Yu 《Journal of Dispersion Science and Technology》2013,34(4):568-575
A series of anionic Gemini surfactants called alkanediyl-α,ω-bis(m-octylphenoxy sulfonate) with different length of (CH2)x spacer, C8CxC8 (x = 2, 4, 6, 8), have been synthesized from 4-n-octylphenol and their basic physicochemical properties are investigated. The results indicate that they are different from cationic Gemini surfactants called alkanediyl-α,ω-bis(dimethyldodecylammonium bromide), 12-(CH2)s-12, in the literature. It is found that as the carbon atom number of the spacer increases, the cmc (critical micelle concentration) decreases gradually, and the surface area per molecule (Amin) decreases initially and then increases. The breakpoints appear at number 4 of carbon atom in the spacer. Though the length of the spacer is different for the Gemini surfactants from C8C2C8 to C8C6C8, there is no obvious change on the micropolarity. 相似文献
953.
Ewa Białecka‐Florjańczyk Irma Śledzińska Ewa Górecka Jan Przedmojski 《Liquid crystals》2013,40(4):401-406
A series of 4‐decyloxy‐4′‐hydroxybiphenyl esters of α,ω‐alkanedicarboxylic acids containing two mesogenic units connected by a methylene spacer was synthesized. The mesogenic properties of the compounds were investigated by polarising optical microscopy, differential scanning calorimetry and X‐ray diffraction methods. A strong influence of the spacer length and its parity on the mesomorphic properties was found. A dramatic odd–even effect was observed for the clearing temperatures and entropies. Compounds with an even number of carbon atoms in the methylene spacer formed tilted smectic phases, whereas compounds with an odd number of carbon atoms in the spacer exhibited the B4 phase, characteristic of bent‐shaped molecules. 相似文献
954.
Abstract Addition of amines and of hydrogenphosphonates on the carbon-carbon double bond belonging to vinyl-phosphoranes is examined. The stereochemistry and reactivity of the saturated adducts obtained is rationalized. Alcoholis of the P—C bond is also studied. 相似文献
955.
A novel organic fluorophor with high solid state luminescent efficiency based on 1,4-bis(2,2-di(pyridin-2-yl)- vinyl)benzene (BDP2VB) was designed and synthesized. It emits faintly in solution, but becomes a strong emitter in the aggregate state, demonstrating its aggregation induced emission (AIE) property. According to the crystal struc- ture analysis, J-type aggregation was formed in the packing mode of the molecule, which was demonstrated to be beneficial to gain high fluorescent quantum efficiency in solid state. Additionally, the emission color of BDP2VB can change dramatically in solid state as well as in solution by the protonation stimuli. 相似文献
956.
957.
With the firm demonstration of the in vivo presence and biological functions of many non‐B DNA structures, it is of great significance to understand their physiological roles from the perspective of structural conformation, stability, and transition kinetics. Although relatively simple in primary sequences compared to proteins, non‐B DNA species show rather versatile conformations and dynamic transitions. As the most‐studied non‐B DNA species, the G‐quadruplex displays a myriad of conformations that can interconvert between each other in different solutions. These features impose challenges for ensemble‐average techniques, such as X‐ray crystallography, NMR spectroscopy, and circular dichroism (CD), but leave room for single‐molecular approaches to illustrate the structure, stability, and transition kinetics of individual non‐B DNA species in a solution mixture. Deconvolution of the mixture can be further facilitated by statistical data treatment, such as iPoDNano (i ntegrated po pulation d econvolution with nano meter resolution), which resolves populations with subnanometer size differences. This Personal Account summarizes current mechanical unfolding and refolding methods to interrogate single non‐B DNA species, with an emphasis on DNA G‐quadruplexes and i‐motifs. These single‐molecule studies start to demonstrate that structures and transitions in non‐B DNA species can approach the complexity of those in RNA or proteins, which provides solid justification for the biological functions carried out by non‐B DNA species. 相似文献
958.
959.
In this study, we for the first time presented an efficient, accurate, rapid, simple and ultrasensitive detection system for small molecule ochratoxin A (OTA) by using the integration of loop-mediated isothermal amplification (LAMP) technique and subsequently direct readout of LAMP amplicons with a signal-on electrochemiluminescent (ECL) system. Firstly, the dsDNA composed by OTA aptamer and its capture DNA were immobilized on the electrode. After the target recognition, the OTA aptamer bond with target OTA and subsequently left off the electrode, which effectively decreased the immobilization amount of OTA aptamer on electrode. Then, the remaining OTA aptamers on the electrode served as inner primer to initiate the LAMP reaction. Interestingly, the LAMP amplification was detected by monitoring the intercalation of DNA-binding Ru(phen)32+ ECL indictors into newly formed amplicons with a set of integrated electrodes. The ECL indictor Ru(phen)32+ binding to amplicons caused the reduction of the ECL intensity due to the slow diffusion of Ru(phen)32+–amplicons complex to the electrode surface. Therefore, the presence of more OTA was expected to lead to the release of more OTA aptamer, which meant less OTA aptamer remained on electrode for producing LAMP amplicons, resulting in less Ru(phen)32+ interlaced into the formed amplicons within a fixed Ru(phen)32+ amount with an obviously increased ECL signal input. As a result, a detection limit as low as 10 fM for OTA was achieved. The aptasensor also has good reproducibility and stability. 相似文献
960.
Mohammad Reza Rezapour Arunkumar Chitteth Rajan Kwang S. Kim 《Journal of computational chemistry》2014,35(26):1916-1920
In molecular electronics, the conductance strongly depends on the frontier energy levels and spatial orientations of molecules. Utilizing these features, we investigate the electron transport characteristics of conjugated molecules attached on an armchair graphene nanoribbon. The resulting sharp reduction in the transmission which represents molecular fingerprints and the change of the transmission depending on the molecular orientation, are examined in accordance with a unified picture of the Fano–Anderson model. These characteristics, being unique for each molecule, would be applicable to molecular recognition and configurational analysis. © 2014 Wiley Periodicals, Inc. 相似文献