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21.
A novel membrane sensor for selective monitoring of iodide, consisting of a triiodide‐ketoconazole ion pair complex dispersed in a PVC matrix, plasticized with a mixture of 2‐nitrophenyl octyl ether and dioctylphtalate with unique selectivity toward iodide ions, is described. The influence of membrane composition, pH of test solution and foreign ions on the electrode performance were investigated. The optimized membrane demonstrates a near‐Nernstian response for iodide ions over a wide linear range from 1.0 × 10?2 to 1.0 × 10?5 M, at 25 ± 1 °C. The electrode could be used over a wide pH range 3–10 and has the advantages of high selectivity, fast response time and good lifetime (over 4 months). It was successfully used as indicator electrode in potentiometric titrations and direct potentiometric assay of iodide ions. 相似文献
22.
Xu Q Tanaka K Mori M Helaleh MI Hu W Hasebe K Toada H 《Journal of chromatography. A》2003,997(1-2):183-190
A monolithic ODS-silica gel column modified by saturating it with lithium dodecylsulfate (Li-DS) was used to demonstrate the high-speed separation of H+ from other mono- and divalent cations, such as Na+, NH4+, K+, Mg2+ and Ca2+ using ion chromatography (IC). Using a 5 mM EDTA-2K solution containing 0.10 mM Li-DS (pH 4.80) as eluent, H+ was eluted with a sharp and symmetrical peak within 1.0 min before other cations at a flow-rate of 1.5 ml min(-1). The rapid elution of H+ and its conductimetric detection could be attributed to the presence of EDTA (HY2-), which can convert H+ ions as anions. i.e. H(+) + H2Y(2-) --> H3Y(-). The acidity of rainwater and deionized water samples was determined using this IC system with satisfactory results. 相似文献
23.
The possibility of using the NMR chemical shift to evaluate and develop intermolecular potentials for cross-interactions between polar and nonpolar molecules has been examined using the method of molecular dynamics. Such interaction potential models are known to be notoriously difficult to develop. Our work has shown that chemical shift can be obtained quite efficiently in simulations and converges much faster than other properties traditionally used for such evaluations (for example, the infinite dilution activity coefficients, Henry’s constants or the solubility of solutes in solvents). We have also found chemical shift to be quite sensitive to the intermolecular potentials which makes it a rather promising property to investigate polar–nonpolar interactions in fluids. 相似文献
24.
A new synthetic procedure has been developed in Mn cluster chemistry involving reductive aggregation of permanganate (MnO4-) ions in MeOH in the presence of benzoic acid, and the first products from its use are described. The reductive aggregation of NBu(n)4MnO4 in MeOH/benzoic acid gave the new 4Mn(IV), 8Mn(III) anion [Mn12O12(OMe)2(O2CPh)16(H2O)2]2-, which was isolated as a mixture of two crystal forms (NBu(n)4)2[Mn12O12(OMe)2(O2CPh)16(H2O)2].2H2O.4CH2Cl2 (1a) and (NBu(n)4)2[Mn12O12(OMe)2(O2CPh)16(H2O)2].2H2O.CH2Cl2 (1b). The anion of 1 contains a central [Mn(IV)4(mu3-O)2(mu-O)2(mu-OMe)2]6+ unit surrounded by a nonplanar ring of eight Mn(III) atoms that are connected to the central Mn4 unit by eight bridging mu3-O2- ions. This compound is very similar to the well-known [Mn12O12(O2CR)16(H2O)4] complexes (hereafter called "normal Mn12"), with the main difference being the structure of the central cores. Longer reaction times (approximately 2 weeks) led to isolation of polymeric [Mn(OMe)(O2CPh)2]n2, which contains a linear chain of repeating [Mn(III)(mu-O2CPh)2(mu-OMe)Mn(III)] units. The chains are parallel to each other and interact weakly through pi-stacking between the benzoate rings. When KMnO4 was used instead of NBu(n)4MnO4, two types of compounds were obtained, [Mn12O12(O2CPh)16(H2O)4] (3), a normal Mn12 complex, and [Mn4O2(O2CPh)8(MeOH)4].2MeOH (4.2MeOH), a new member of the Mn4 butterfly family. The cyclic voltammogram of 1 exhibits three irreversible processes, two reductions and one oxidation. One-electron reduction of 1 by treatment with 1 equiv of I- in CH2Cl2 gave (NBu(n)4[Mn12O12(O2CPh)16(H2O)3].6CH2Cl2 (5.6CH2Cl2), a normal Mn12 complex in a one-electron reduced state. The variable-temperature magnetic properties of 1, 2, and 5 were studied by both direct current (dc) and alternating current (ac) magnetic susceptibility measurements. Variable-temperature dc magnetic susceptibility studies revealed that (i) complex 1 possesses an S = 6 ground state, (ii) complex 2 contains antiferromagnetically coupled chains, and (iii) complex 5 is a typical [Mn12]- cluster with an S = 19/2 ground state. Variable-temperature ac susceptibility measurements suggested that 5 and both isomeric forms of 1 (1a,b) are single-molecule magnets (SMMs). This was confirmed by the observation of hysteresis loops in magnetization vs dc field scans. In addition, 1a,b, like normal Mn12 clusters, display both faster and slower relaxing magnetization dynamics that are assigned to the presence of Jahn-Teller isomerism. 相似文献
25.
Flow injection analysis with on-line preconcentration using a minicolumn loaded with dialkyldithiocarbamate immobilized on controlled pore glass is described for the determination of Rh(III), Co2+, Cu2+, Hg2+, and Hg22+. The detection limits range from 0.05 ng ml−1 for Cu2+ to 50 ng ml−1 for Hg2+ for 5- or 10-ml samples, improvement of 2–3 orders of magnitude compared with direct injection. The operating conditions are optimized and the effects of interferents are studied. The capacity of the collector varied from 0.9 mmol g−1 for Rh(III) to ca 4 mmol g−1 (Co2+, Cu2+, Hg2+). 相似文献
26.
The dissolution of zinc in 0.48–1.49M HNO3 was studied at 15–25°C, by following simultaneously the concentration changes of the reactants (Zn and HNO3), intermediate (HNO2) and product (Zn2+) with time. Explicit mechanisms were suggested for the dissolution of zinc in nitric acid. The kinetics of the dissolution process show that it is of the first-order with respect to [Zn] and [HNO2]. The data obtained show that the dissolution process is diffusion-controlled. The mechanism of zinc dissolution is compared with the mechanism of copper dissolution.
Die Kinetik der Auflösung von Zink in Salpetersäure
Zusammenfassung Die Auflösung von Zink in 0.48–1.49M HNO3 wurde bei 15–25°C mittels gleichzeitiger Verfolgung der Konzentrationsänderungen der Reaktanden (Zn und HNO3), des intermediären HNO2 und des Produkts Zn2+ untersucht. Es wird ein Mechanismus vorgeschlagen. Die Kinetik der Auflösung ist erster Ordnung bezüglich [Zn] und [HNO2]. Die Daten zeigen, daß der Auflösungsvorgang diffusionskontrolliert ist. Der Mechanismus der Auflösung von Zink wird mit dem der Kupferauflösung verglichen.相似文献
27.
Farah Diab Hawraa Zbeeb Francesca Baldini Piero Portincasa Mohamad Khalil Laura Vergani 《Molecules (Basel, Switzerland)》2022,27(15)
Numerous plants, plant extracts, and plant-derived compounds are being explored for their beneficial effects against overweight and liver diseases. Obesity is associated with the increased prevalence of non-alcoholic fatty liver disease (NAFLD), becoming the most common liver disease in Western countries. Obesity and NAFLD are closely associated with many other metabolic alternations such as insulin resistance, diabetes mellitus, and cardiovascular diseases. Many herbs of the Lamiaceae family are widely employed as food and spices in the Mediterranean area, but also in folk medicine, and their use for the management of metabolic disorders is well documented. Hereby, we summarized the scientific results of the medicinal and nutraceutical potential of plants from the Lamiaceae family for prevention and mitigation of overweight and fatty liver. The evidence indicates that Lamiaceae plants may be a cost-effective source of nutraceuticals and/or phytochemicals to be used in the management of metabolic-related conditions such as obesity and NAFLD. PubMed, Google Scholar, Scopus, and SciFinder were accessed to collect data on traditional medicinal plants, compounds derived from plants, their reported anti-obesity mechanisms, and therapeutic targets. 相似文献
28.
Hany Ezzat Khalil Miada F. Abdelwahab Promise Madu Emeka Lorina I. Badger-Emeka Krishnaraj Thirugnanasambantham Hairul-Islam Mohamed Ibrahim Sara Mohamed Naguib Katsuyoshi Matsunami Nada M. Abdel-Wahab 《Molecules (Basel, Switzerland)》2022,27(9)
Diabetes mellitus (DM) is a complicated condition that is accompanied by a plethora of metabolic symptoms, including disturbed serum glucose and lipid profiles. Several herbs are reputed as traditional medicine to improve DM. The current study was designed to explore the chemical composition and possible ameliorative effects of Ocimum forskolei on blood glucose and lipid profile in high-fat diet/streptozotocin-induced diabetic rats and in 3T3-L1 cell lines as a first report of its bioactivity. Histopathological study of pancreatic and adipose tissues was performed in control and treatment groups, along with quantification of glucose and lipid profiles and the assessment of NF-κB, cleaved caspase-3, BAX, and BCL2 markers in rat pancreatic tissue. Glucose uptake, adipogenic markers, DGAT1, CEBP/α, and PPARγ levels were evaluated in the 3T3-L1 cell line. Hesperidin was isolated from total methanol extract (TME). TME and hesperidin significantly controlled the glucose and lipid profile in DM rats. Glibenclamide was used as a positive control. Histopathological assessment showed that TME and hesperidin averted necrosis and infiltration in pancreatic tissues, and led to a substantial improvement in the cellular structure of adipose tissue. TME and hesperidin distinctly diminished the mRNA and protein expression of NF-κB, cleaved caspase-3, and BAX, and increased BCL2 expression (reflecting its protective and antiapoptotic actions). Interestingly, TME and hesperidin reduced glucose uptake and oxidative lipid accumulation in the 3T3-L1 cell line. TME and hesperidin reduced DGAT1, CEBP/α, and PPARγ mRNA and protein expression in 3T3-L1 cells. Moreover, docking studies supported the results via deep interaction of hesperidin with the tested biomarkers. Taken together, the current study demonstrates Ocimum forskolei and hesperidin as possible candidates for treating diabetes mellitus. 相似文献
29.
Gunnar Aksnes Fayez Y. Khalil Piotr J. Majewski 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):157-161
Abstract This study reports rate data of the alkoxide promoted decomposition of triphenyl 3-hydroxypropyl phosphonium chloride, diphenyl di(3-hydroxypropyl)phosphonium chloride, and tetraphenyl phosphonium bromide. Comparison of kinetics, rate constants, and activation parameters of the alkoxide promoted decompositions points to different mechanism as compared to the hydroxyl promoted reaction. The alkoxide reaction is believed to proceed via a hexacovalent intermediate. Reasons for the hexacovalent route are discussed. 相似文献
30.
Two terthiophenes incorporating the synthon 3,4-(1,2-phenylenedioxy)thiophene (PheDOT) have been developed. Specifically, 2,5-bisthienyl-3,4-(1,2-phenylenedioxy)thiophene (BTh-PheDOT 1) and 2,5-bisethylenedioxythienyl-3,4-(1,2-phenylenedioxy)thiophene (BEDOT-PheDOT 2) were electropolymerized to form electroactive polymer films (P1 and P2) that switched between two highly colored states with the more electron-rich EDOT derivative P2 observed to switch at a lower potential. Additionally, both P1 and P2 displayed moderate to low optical bandgaps of 1.8 and 1.6 eV, respectively. Crystal structures of BTh-PheDOT showed the monomer to be nearly planar with π -stacking observable between monomers. These findings demonstrate the potential of PheDOT as an electroactive synthon for the formation of well-ordered systems. 相似文献