全文获取类型
收费全文 | 4275篇 |
免费 | 143篇 |
国内免费 | 42篇 |
专业分类
化学 | 2855篇 |
晶体学 | 34篇 |
力学 | 155篇 |
数学 | 410篇 |
物理学 | 927篇 |
综合类 | 79篇 |
出版年
2024年 | 19篇 |
2023年 | 36篇 |
2022年 | 257篇 |
2021年 | 204篇 |
2020年 | 146篇 |
2019年 | 138篇 |
2018年 | 164篇 |
2017年 | 116篇 |
2016年 | 164篇 |
2015年 | 159篇 |
2014年 | 161篇 |
2013年 | 315篇 |
2012年 | 257篇 |
2011年 | 284篇 |
2010年 | 161篇 |
2009年 | 142篇 |
2008年 | 151篇 |
2007年 | 174篇 |
2006年 | 131篇 |
2005年 | 136篇 |
2004年 | 87篇 |
2003年 | 79篇 |
2002年 | 73篇 |
2001年 | 74篇 |
2000年 | 54篇 |
1999年 | 63篇 |
1998年 | 27篇 |
1997年 | 27篇 |
1996年 | 43篇 |
1995年 | 40篇 |
1994年 | 27篇 |
1993年 | 31篇 |
1992年 | 34篇 |
1991年 | 41篇 |
1990年 | 19篇 |
1989年 | 21篇 |
1988年 | 28篇 |
1987年 | 26篇 |
1986年 | 26篇 |
1985年 | 38篇 |
1984年 | 23篇 |
1983年 | 23篇 |
1982年 | 22篇 |
1981年 | 11篇 |
1980年 | 28篇 |
1979年 | 21篇 |
1978年 | 27篇 |
1977年 | 28篇 |
1976年 | 18篇 |
1968年 | 10篇 |
排序方式: 共有4460条查询结果,搜索用时 23 毫秒
151.
McAlister proved that a necessary and sufficient condition for a regular semigroup S to be locally inverse is that it can be embedded as a quasi-ideal in a semigroup T which satisfies the following two conditions: (1) T = TeT, for some idempotent e; and (2) eTe is inverse. We generalise this result to the class of semigroups with local units in which all local submonoids have commuting idempotents. 相似文献
152.
Syed Hamad Bukhari Muhammad Iqbal Hussain Salman Naeem Khan Muhammad Ashfaq Ahmad 《Optik》2012,123(24):2288-2291
Nonclassical features of Schrödinger cat state with two-mode superposition state based on two coherent states π out of phase by fixing the relative phase equal to average photon number are discussed. Study of two-mode quadrature squeezing, oscillatory and sub-Poissonian photon statistics show that nonclassicality exists for these states. However, it is observed that the considered states do not violates the Cauchy–Schwarz inequality. Furthermore, simultaneously existence of quadrature squeezing and sub-Poissonian photon statistics shows that these states have more nonclassical features than that of famous even and odd coherent states. 相似文献
153.
M. A. Majeed?Khan M. Wasi?Khan Mansour Alhoshan M. S. AlSalhi A. S. Aldwayyan 《Applied Physics A: Materials Science & Processing》2010,100(1):45-51
Pure and Co-doped ZnO nanostructured samples have been synthesized by a chemical route. We have studied the structural and
optical properties of the samples by using X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), field-emission
transmission electron microscope (FETEM), energy-dispersive X-ray (EDX) analysis and UV–VIS spectroscopy. The XRD patterns
show that all the samples are hexagonal wurtzite structures. Changes in crystallite size due to mechanical activation were
also determined from X-ray measurements. These results were correlated with changes in particle size followed by SEM and TEM.
The average crystallite sizes obtained from XRD were between 20 to 25 nm. The TEM images showed the average particle size
of undoped ZnO nanostructure was about 20 nm whereas the smallest average grain size at 3% Co was about 15 nm. Optical parameters
such as absorption coefficient (α), energy band gap (E
g
), the refractive index (n), and dielectric constants (σ) have been determined using different methods. 相似文献
154.
Shwetha U. R Maha Abdallah Alnuwaiser Latha M. S Virupaxappa S. Betageri Shilpa V. A M. Ijaz Khan Kamel Guedri 《印度化学会志》2022,99(9):100606
The present research highlights physical significance of green combination of metal oxide nanomaterials utilizing medicinal plant which has widely analyzed in different medical applications i.e., medicinal science, therapeutics. In this paper, we discussed environmentally benign approach for synthesizing silver doped copper oxide nanoparticles (Ag–CuO NPs) utilizing (ACLE). Scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) were utilized to confirm the size, crystalline structure and surface morphology of the obtained nanomaterials. The monoclinic crystalline structure of the Ag–CuO NPs as produced was revealed by XRD patterns. Morphological analysis disclosed the nano-based spherical configuration of Ag–CuO NPs, as well as their morphology and elemental composition. The anti-diabetic effect of Ag–CuO NPs was further investigated utilizing a yeast cell model and amylase inhibition. Here, a decrease in intracellular glucose and a delay in carbohydrate digestion indicate promising antidiabetic action. Furthermore, the prepared nanomaterial showed anticancer potential against the MCF-7 cancer cell line, with an IC 50 value of 11.21 g/ml. 相似文献
155.
This paper presents liquid chromatography/mass spectrometry (LC/MS) and liquid chromatography/tandem mass spectrometry (LC/MS/MS) approaches for the rapid characterization of three urinary isomeric metabolites and their two precursor metabolites of SYN-2836, a novel antifungal agent, in dogs administered multiple oral doses of the agent (30 mg kg(-1) day(-1)). A collection of correlative data regarding the SYN-2836 metabolites was obtained by LC/MS and LC/MS/MS performed under complementary conditions such as the columns (C(18) vs cyano type), the mobile phase systems (acetonitrile-water-formic acid vs acetonitrile-water-ammonium acetate) and the electrospray ionization modes (positive vs negative). Metabolite identification was accomplished based on not only the LC/MS/MS data (product ion spectra) but also the LC/MS data indicating chromatographic behaviors of the metabolites. SYN-2836 and SYN-2869, an analog of the former, showed almost the same metabolic pathways following the same multiple-dose administration of the individual agents to the dogs. Therefore, correlation analysis in product ion spectra between corresponding metabolites of SYN-2836 and SYN-2869, and also in metabolic pathways between the two agents, was strategically used to facilitate the identification of the SYN-2836 (and SYN-2869 if necessary) metabolites. For the reason that various elucidation strategies were used complementarily, the chemical structures of the metabolites were unambiguously attained and the isomeric metabolites were explicitly differentiated without the use of other analytical methods. The methodologies used in this study may be applicable to metabolite screening of several structurally related agents simultaneously, promoting lead finding and optimization of drug candidates using a metabolism-based approach. 相似文献
156.
Khan M Brunklaus G Enkelmann V Spiess HW 《Journal of the American Chemical Society》2008,130(5):1741-1748
13C-CPMAS and other solid-state NMR methods have been applied to monitor the solid-state reactions of trans-cinnamic acid derivatives, which are the pioneer and model compounds in the field of topochemistry previously studied by X-ray diffraction, AFM, and vibrational spectroscopy. Single-crystal X-ray analyses of photoirradiated alpha-trans-cinnamic acid where the monomers are arranged in a head-to-tail manner have revealed the formation of a centrosymmetric alpha-truxillic acid photodimer. For a centrosymmetric dimer, however, two cyclobutane carbon signals and one carbonyl carbon signal were expected apart from other aromatic carbon signals. Instead, four cyclobutane and two carbonyl carbon signals were observed suggesting the formation of a non-centrosymmetric photodimer. Removing hydrogen bonds from the system by esterfication of alpha-truxillic acid yield a centrosymmetric photodimer. Careful analysis of the obtained products via solid-state NMR clearly showed that the observed peak splittings in the 13C-CPMAS spectra did not originate from packing effects but rather result from asymmetric hydrogen bonds distorting the local symmetry. Further evidence of this rather dynamic hydrogen-bonding stems from high-temperature X-ray data revealing that only the joint approach of both X-ray analysis and solid-state NMR at similar temperatures allows for the successful characterization of dynamic processes occurring in topochemical reactions, thus, providing detailed insight into the reaction mechanism of organic solid-state transformations. 相似文献
157.
Bilal Ahmad Ghalloo Kashif-ur-Rehman Khan Saeed Ahmad Hanan Y. Aati Jawaher H. Al-Qahtani Barkat Ali Imran Mukhtar Musaddique Hussain Muhammad Nadeem Shahzad Imtiaz Ahmed 《Molecules (Basel, Switzerland)》2022,27(3)
Dracaena reflexa, a traditionally significant medicinal plant, has not been extensively explored before for its phytochemical and biological potential. The present study was conducted to evaluate the bioactive phytochemicals and in vitro biological activities of D. reflexa, and perform in silico molecular docking validation of D. reflexa. The bioactive phytochemicals were assessed by preliminary phytochemical testing, total bioactive contents, and GC-MS analysis. For biological evaluation, the antioxidant (DPPH, ABTS, CUPRAC, and ABTS), antibacterial, thrombolytic, and enzyme inhibition (tyrosinase and cholinesterase enzymes) potential were determined. The highest level of total phenolic contents (92.72 ± 0.79 mg GAE/g extract) was found in the n-butanol fraction while the maximum total flavonoid content (110 ± 0.83 mg QE/g extract) was observed in methanolic extract. The results showed that n-butanol fraction exhibited very significant tyrosinase inhibition activity (73.46 ± 0.80) and acetylcholinesterase inhibition activity (64.06 ± 2.65%) as compared to other fractions and comparable to the standard compounds (kojic acid and galantamine). The methanolic extract was considered to have moderate butyrylcholinesterase inhibition activity (50.97 ± 063) as compared to the standard compound galantamine (53.671 ± 0.97%). The GC-MS analysis of the n-hexane fraction resulted in the tentative identification of 120 bioactive phytochemicals. Furthermore, the major compounds as identified by GC-MS were analyzed using in silico molecular docking studies to determine the binding affinity between the ligands and the enzymes (tyrosinase, acetylcholinesterase, and butyrylcholinesterase enzymes). The results of this study suggest that Dracaena reflexa has unquestionable pharmaceutical importance and it should be further explored for the isolation of secondary metabolites that can be employed for the treatment of different diseases. 相似文献
158.
Fahadul Islam Saikat Mitra Talha Bin Emran Zidan Khan Nikhil Nath Rajib Das Rohit Sharma Ahmed Abdullah Al Awadh Moon Nyeo Park Bonglee Kim 《Molecules (Basel, Switzerland)》2022,27(17)
Gastric cancer is one of the most common cancers of the gastrointestinal tract. Although surgery is the primary treatment, serious maladies that dissipate to other parts of the body may require chemotherapy. As there is no effective procedure to treat stomach cancer, natural small molecules are a current focus of research interest for the development of better therapeutics. Chemotherapy is usually used as a last resort for people with advanced stomach cancer. Anti-colon cancer chemotherapy has become increasingly effective due to drug resistance and sensitivity across a wide spectrum of drugs. Naturally-occurring substances have been widely acknowledged as an important project for discovering innovative medications, and many therapeutic pharmaceuticals are made from natural small molecules. Although the beneficial effects of natural products are as yet unknown, emerging data suggest that several natural small molecules could suppress the progression of stomach cancer. Therefore, the underlying mechanism of natural small molecules for pathways that are directly involved in the pathogenesis of cancerous diseases is reviewed in this article. Chemotherapy and molecularly-targeted drugs can provide hope to colon cancer patients. New discoveries could help in the fight against cancer, and future stomach cancer therapies will probably include molecularly formulated drugs. 相似文献
159.
Utilizing self-assembly to create supramolecular structures is an active area at this time. Hybrid materials created by blending or doping, e.g., organic/inorganic or donor/acceptor complexes are of great interest in the design of novel materials systems. The effect of mixing of any two self-assembling molecules to modify the properties and to understand if the process of blending changes the nature of the self-assembly would be of interest. We discuss here the effect of blending of two (hydrogen bond mediated) self-assembling homologous molecules on the structure and morphology. Materials that are candidate vehicles for phase-change inkjet technology, biscarbamates with alkyl side chains, are chosen for this study. Thermal analysis and IR spectra indicate that, when two biscarbamates differing only in the length of the alkyl chain are blended, the two components are immiscible, although they are chemically similar. There is no intercalation of the alkyl chains and cocrystallization. They are thus an example of a self-sorting system. The extent of hydrogen bonding and the packing of the alkyl chains are not affected. However, each serve as a nucleating agent and reduce the size of the spherulites and crystallinity. The spherulitic growth rate decreases upon blending. Partial melting experiments show that the spherulites of each component do not form independently, but are intermixed, implying that one acts as the nucleating sites for the other. Thus, although these are self-sorting, the components in the mixture affect the morphology of each other upon crystallization. The behavior of this small molecule mixture is compared with those of hydrogen-bonded polymer blends. Studies of this nature on blends of self-assembling molecules are expected to be important in materials design for optimizing properties. 相似文献
160.
Sander M Jarrosson T Chuang SC Khan SI Rubin Y 《The Journal of organic chemistry》2007,72(8):2724-2731
In a quest to form wider openings within the cage of the fullerene C60 through controlled bond-breaking reactions, we have examined the double saturation of adjacent C=C bonds within a six-membered ring of C60. We have investigated the double Diels-Alder cycloaddition of two tethered isobenzofurans to the fullerene C60. We obtained cis-1 adducts in good yields after reacting the methylene- or quinoxaline-tethered bis(isobenzofuran) precursors 2a-k with parent 3,6-dihydro-1,2,4,5-tetrazine (3b). The X-ray structure of the methylene-tethered bis(isobenzofuran)-C60 adduct 4b has been obtained; four-eclipsed substituents are held rigidly by the bicyclic addends. The cis-1 bis(isobenzofuran) bisadducts 4b and 4e-j are kinetically far more stable toward thermal retro-Diels-Alder fragmentation than are mono(isobenzofuran) adducts of C60, in solution and in the solid state as determined by 1H NMR spectroscopy or thermogravimetric analysis. A methodology for the reversible solubilization of other fullerene derivatives based on this work is also presented. 相似文献