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991.
A concise, diastereoselective total synthesis of (±)-cortistatin J has been completed in 20 steps from furan. Key steps include an intramolecular [4 + 3] cyclization of a disubstituted furan with a (Z)-2-(trialkylsilyloxy)-2-enal to construct the tetracyclic core and a (Z)-vinylsilane/iminium ion cyclization to form the A ring. 相似文献
992.
White Emitters by Tuning the Excited‐State Intramolecular Proton‐Transfer Fluorescence Emission in 2‐(2′‐Hydroxybenzofuran)benzoxazole Dyes 下载免费PDF全文
Karima Benelhadj Wenziz Muzuzu Dr. Julien Massue Dr. Pascal Retailleau Dr. Azzam Charaf‐Eddin Dr. Adèle D. Laurent Prof. Denis Jacquemin Dr. Gilles Ulrich Dr. Raymond Ziessel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(40):12843-12857
The synthesis, structural, and photophysical properties of a new series of original dyes based on 2‐(2′‐hydroxybenzofuran)benzoxazole (HBBO) is reported. Upon photoexcitation, these dyes exhibit intense dual fluorescence with contribution from the enol (E*) and the keto (K*) emission, with K* being formed through excited‐state intramolecular proton transfer (ESIPT). We show that the ratio of emission intensity E*/K* can be fine‐tuned by judiciously decorating the molecular core with electron‐donating or ‐attracting substituents. Push–pull dyes 9 and 10 functionalized by a strong donor (nNBu2) and a strong acceptor group (CF3 and CN, respectively) exhibit intense dual emission, particularly in apolar solvents such as cyclohexane in which the maximum wavelength of the two bands is the more strongly separated. Moreover, all dyes exhibit strong solid‐state dual emission in a KBr matrix and polymer films with enhanced quantum yields reaching up to 54 %. A wise selection of substituents led to white emission both in solution and in the solid state. Finally, these experimental results were analyzed by time‐dependent density functional theory (TD‐DFT) calculations, which confirm that, on the one hand, only E* and K* emission are present (no rotamer) and, on the other hand, the relative free energies of the two tautomers in the excited state guide the ratio of the E*/K* emission intensities. 相似文献
993.
Raymond J. Ritchie 《Photochemistry and photobiology》2013,89(5):1143-1162
Photosynthetic bacteria are attractive for biotechnology because they produce no oxygen and so H2‐production is not inhibited by oxygen as occurs in oxygenic photoorganisms. Rhodopseudomonas palustris and Afifella marina containing BChl a can use irradiances from violet near‐UV (VNUV) to orange (350–650 nm) light and near‐infrared (NIR) light (762–870 nm). Blue diode‐based pulse amplitude modulation technology was used to measure their photosynthetic electron transport rate (ETR). ETR vs Irradiance curves fitted the waiting‐in‐line model—ETR = (ETRmax × E/Eopt) × exp (1 ? E/Eopt). The equation was integrated over pond depth to calculate ETR of Afifella and Rhodopseudomonas in a pond up to 30 cm deep (A376, 1 cm = 0.1). Afifella saturates at low irradiances and so photoinhibition results in very low photosynthesis in a pond. Rhodopseudomonas saturates at ≈15% sunlight and shows photoinhibition in the surface layers of the pond. Total ETR is ≈335 μmol (e?) m?2 s?1 in NUV + photosynthetically active radiation light (350–700 nm). Daily ETR curves saturate at low irradiances and have a square‐wave shape: ≈11–13 mol (e?) m?2 day?1 (350–700 nm). Up to 20–24% of daily 350–700 nm irradiance can be converted into ETR. NIR is absorbed by water and so competes with the bacterial RC‐2 photosystem for photons. 相似文献
994.
During the past decade, methyl 7-(5-oxocyclopentenyl)heptanoate (6) has been frequently used as a key intermediate in prostaglandin synthesis.1 Although keto ester 6 can be readily obtained by treatment of traumatic acid (5) with polyphosphoric acid followed by esterification with methanolic hydrochloric acid,2 this approach is not attractive for large-scale synthesis due to the expense of the latter natural product (5). Recently Salomon and Reuter have reported1 an alternate route to synthon 6 based on a starting material derived from aleuritic acid, a major component of shellac. 相似文献
995.
Net Promoter Score, touted as the “single customer metric you need” and calculated from customers' answer to one simple question about their loyalty, has been in use since 2003 and adopted in a wide variety of settings. However, it has not lived up to its claimed benefits. This article evaluates the NPS approach in terms of its positive and negative results. This article is for people interested in NPS, still considering implementing NPS in their company, or interested in its technical underpinnings. It points out the benefits and shortcomings and explains why, and it describes what can be done to achieve the outcomes NPS theory claimed it would produce, but has not. The article is written in two parts for quite distinct audiences: firstly, for executives and managers who need customer data and information to make marketing decisions; and secondly, for market researchers, statisticians, and business analysts who are responsible for capturing and providing reliable, understandable, and meaningful customer data to the executives and managers who need the information. Consequently, the two sections are written in two different styles. The first section takes the form of a summary for managers and executives of our findings and recommendations in language aimed at business leaders; the second section provides a detailed analysis and critical review of NPS for market researchers, statisticians, and business analysts. Both sections present a better solution than NPS for understanding what customers value, delivering the best value to customers, winning market share, and creating truly loyal customers. 相似文献
996.
Biomolecular phase transitions play an important role in organizing cellular processes in space and time. Methods and tools for studying these transitions, and the intrinsically disordered proteins (IDPs) that often drive them, are typically less developed than tools for studying their folded protein counterparts. In this perspective, we assess the current landscape of chemical tools for studying IDPs, with a specific focus on protein liquid–liquid phase separation (LLPS). We highlight methodologies that enable imaging and spectroscopic studies of these systems, including site-specific labeling with small molecules and the diverse range of capabilities offered by inteins and protein semisynthesis. We discuss strategies for introducing post-translational modifications that are central to IDP and LLPS function and regulation. We also investigate the nascent field of noncovalent small-molecule modulators of LLPS. We hope that this review of the state-of-the-art in chemical tools for interrogating IDPs and LLPS, along with an associated perspective on areas of unmet need, can serve as a valuable and timely resource for these rapidly expanding fields of study.Chemical tools provide the ability to illuminate and manipulate the behavior of intrinsically disordered proteins and their phase transitions. 相似文献
997.
Multilayer perceptron is composed of massive distributed neural processors interconnected. The nonlinear dynamic components in these processors expand the input data into a linear combination of synapses. However, the nonlinear mapping ability of original multilayer perceptron is limited when processing high complexity information. The introduction of more powerful nonlinear components (e.g., S-box) to multilayer perceptron can not only reinforce its information processing ability, but also enhance the overall security. Therefore, we combine the methods of cryptography and information theory to design a low-power chaotic S-box (LPC S-box) with entropy coding in the hidden layer to make the multilayer perceptron process information more efficiently and safely. In the performance test, our S-box architecture has good properties, which can effectively resist main known attacks (e.g., Berlekamp Massey-attack and Ronjom–Helleseth attack). This interdisciplinary work can attract more attention from academia and industry to the security of multilayer perceptron. 相似文献
998.
MXenes,a new family of functional two-dimensional(2 D) materials,have shown great potential for an extensive variety of applications within the last decade.Atomic defects and functional groups in MXenes are known to have a tremendous influence on the functional properties.In this review,we focus on recent progress in the characterization of atomic defects and functional group chemistry in MXenes,and how to control them to directly influence various properties(e.g.,electron transport,Li+ adsorption,hydrogen evolution reaction(HER) activity,and magnetism) of 2 D MXenes materials.Dynamic structural transformations such as oxidation and growth induced by atomic defects in MXenes are also discussed.The review thus provides perspectives on property optimization through atomic defect engineering,and bottom-up synthesis methods based on defect-assisted homoepitaxial growth of MXenes. 相似文献
999.
1000.