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61.
Dip-pen nanolithography in tapping mode 总被引:1,自引:0,他引:1
Dip-pen nanolithography (DPN) is becoming a popular nano-patterning technique for depositing materials onto a substrate using the probe of an atomic force microscope (AFM). Here, we demonstrate the deposition of a short synthetic peptide by DPN using the Tapping Mode of AFM rather than the commonly used contact mode. DPN in Tapping Mode requires drive amplitude modifications for deposition, yet allows for gentle imaging of the deposited material and enables deposition on soft surfaces. 相似文献
62.
Patil KJ Pawar RB 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2003,59(6):1289-1297
Near infrared spectra of solution of 6.4 M HDO in D(2)O have been obtained at 15, 25, 30, and 35 degrees C. It was observed that the bands of HDO in D(2)O occur at 1416, 1525, 1556, and 1666 nm, which are in good agreement with the similar data reported earlier by Worley and Klotz. The calculations of enthalpy change for hydrogen bond formation (DeltaH degrees ) yielded the value of -2.5+/-0.4 kcal mol(-1), which is in excellent agreement with the value reported by Walrafen. Similar spectra were recorded for 1 and 2 m 18-crown-6 (18C6) dissolved in the solution of HDO in D(2)O at different temperatures. The band positions remain unchanged, however, the variation of intensity as a function of concentration of 18C6 and temperature clearly indicate that 18C6 acts as a structure making solute. The structural temperature and DeltaH degrees values have been obtained for the 18C6 solutions. These results are explained on the basis of the stabilization of 18C6 in the D(3d) conformation through hydrogen bonding of HDO molecules [doubly hydrogen bonded, i.e. bridging, and singly hydrogen bonded] to the oxygen atoms of 18C6 molecules. Slightly different DeltaH degrees values obtained can be attributed to clathrate like structure at 1 m 18C6 concentration while at 2 m 18C6 concentration it is postulated that the hydrophobic interactions are contributing additionally. 相似文献
63.
Chelsea C. Buck Patrick B. Dennis Maneesh K. Gupta Marcus T. Grant Marquise G. Crosby Joseph M. Slocik Peter A. Mirau Kellie A. Becknell Kristen K. Comfort Rajesh R. Naik 《Macromolecular bioscience》2019,19(3)
The suckerin family of proteins, identified from the squid sucker ring teeth assembly, offers unique mechanical properties and potential advantages over other natural biomaterials. In this study, a small suckerin isoform, suckerin‐12, is used to create enzymatically crosslinked, macro‐scale hydrogels. Upon exposure to specific salt conditions, suckerin‐12 hydrogels contracted into a condensed state where mechanical properties are found to be modulated by the salt anion present. The rate of contraction is found to correlate well with the kosmotropic arm of the Hofmeister anion series. However, the observed changes in hydrogel mechanical properties are better explained by the ability of the salt to neutralize charges in suckerin‐12 by deprotonization or charge screening. Thus, by altering the anions in the condensing salt solution, it is possible to tune the mechanical properties of suckerin‐12 hydrogels. The potential for suckerins to add new properties to materials based on naturally‐derived proteins is highlighted. 相似文献
64.
Narayanan Balaji Bhavesh Babulal Gabani Umesh Todmal Suresh P. Sulochana Neeraj Kumar Saini Rajesh Chandran Ramesh Mullangi 《Biomedical chromatography : BMC》2019,33(3)
We developed and validated a simple, sensitive, selective and reliable LC–ESI‐MS/MS method for direct quantitation of dropropizine enantiomers namely levodropropizine (LDP) and dextrodropropizine (DDP) in rat plasma without the need for derivatization as per regulatory guidelines. Dropropizine enantiomers and carbamazepine (internal standard) were extracted from 50 μL rat plasma using ethyl acetate. LDP and DDP resolved with good baseline separation (Rs = 4.45) on a Chiralpak IG‐3 column. The mobile phase consisted of methanol with 0.05% diethylamine pumped at a flow rate of 0.5 mL/min. Detection and quantitation were done in multiple reaction monitoring mode following the transitions m/z 237 → 160 and 237 → 194 for dropropizine enantiomers and the internal standard, respectively, in the positive ionization mode. The proposed method provided accurate and reproducible results over the linearity range of 3.23–2022 ng/mL for each enantiomer. The intra‐ and inter‐day precisions were in the ranges of 3.38–13.6 and 5.11–13.8 for LDP and 4.19–11.8 and 8.89–10.1 for DDP. Both LDP and DDP were found to be stable under different stability conditions. The method was successfully used in a stereoselective pharmacokinetic study of dropropizine enantiomers in rats following oral administration of racemate dropropizine at 100 mg/kg. The pharmacokinetic results indicate that the disposition of dropropizine enantiomers is not stereoselective and chiral inversion does not occur in rats. 相似文献
65.
[reaction: see text] Lewis acid-promoted addition of allyltri-n-butylstannane to o-quinonediimines afforded tetrahydroquinoxaline derivatives or allylated amides depending on the nature of the substituent on imine nitrogen. 相似文献
66.
The first synthesis of bioactive decytospolides A and B adopting an oxa-Michael addition as the key step is reported. 相似文献
67.
Kalidhasan S Santhana KrishnaKumar A Rajesh V Rajesh N 《Journal of colloid and interface science》2012,367(1):398-408
The molecular interaction of biopolymers with an array of substrates offers interesting insight into the adsorption phenomenon. The present work proposes the preparation and characterization of cellulose-methyltrioctylammonium chloride (MeTOACl)-a room temperature ionic liquid (IL) blend polymeric sorbent and its application for the adsorption of carcinogenic chromium(VI). The blend adsorbent material was synthesized in a relatively green solvent (methylisobutylketone) medium by ultrasonication. The mechanism of interaction of biopolymer with the ionic liquid could be conceptualized as electrostatic attraction, hydrogen bonding, and Van der Waals force of attraction with the hydroxyl groups of cellulose as a bilayer assembly. The composition, crystallinity, and the surface area of the prepared material were comprehensively characterized using FT-IR, solid-state (13)C NMR, TGA, XRD, SEM, EDX, XPS, and BET isotherm study. The adsorption capacity of chromium(VI) calculated from Langmuir isotherm model was found to be 38.94 mg g(-1) with adherence to the second-order kinetics. The study of thermodynamic parameters that affect the sorption process indicated the spontaneity and exothermic nature of adsorption. The green aspect in the methodology is brought out in the regeneration of the adsorbent, where Cr(VI) could be effectively reduced to the less toxic Cr(III) using ascorbic acid. 相似文献
68.
Kumar M Kumar R Bhalla V Sharma PR Kaur T Qurishi Y 《Dalton transactions (Cambridge, England : 2003)》2012,41(2):408-412
A thiacalix[4]arene based fluorescent chemosensor 3 in the cone conformation has been synthesized and its recognition behaviour is evaluated toward various metal ions in mixed aqueous media. The chemosensor 3 showed high selectivity towards Fe(3+) ions by fluorescence quenching of excimer emission. Further, evaluation of the 3·Fe(3+) complex prepared in situ demonstrated great promise for the detection of the Fe(3+) ion in the presence of amino acids, blood serum and bovine serum albumin (BSA) solution. The compound 3 has suitable permeability into the PC3 cells and can be utilized as a Fe(3+) selective sensor in living cells (PC3 cells). 相似文献
69.
Rajendran Manikandan Ramanathan Rajajeyaganthan Ganesan P. Shanmugavel Rajesh 《Journal of Thermal Analysis and Calorimetry》2021,143(4):3009-3021
Journal of Thermal Analysis and Calorimetry - In this work, considering the various practical concerns during storage, processing, handling and emission of flash powder used for making firecracker,... 相似文献
70.
Vidya Rani Chandrasekhar Kesavan Mookkandi Palsamy Ravi Lokesh Daniel Thangadurai T. Indra Gandhi N. Rajesh Jegathalaprathaban Rajagopal Gurusamy 《应用有机金属化学》2019,33(3)
Three new metal complexes [Cu(L)2] (1), [Co(L)2] (2) and [Zn(L)2] (3) have been prepared by the reaction of hydrated salts of metal (II) acetate with new Schiff base ligand HL, [2‐((4‐(dimethylamino)phenylimino)methyl)‐4,6‐di‐t‐butylphenol] and characterized by different physico‐chemical analyses such as elemental analysis, single XRD, 1H NMR, FTIR and UV–Vis spectroscopic techniques. Their biomolecular docking, antimicrobial and cytotoxicity studies have also been demonstrated. The proposed structure of Schiff base ligand HL and complex 2 are confirmed by Single crystal X‐ray crystallography study. This analysis revealed that metal (II) complexes remain in distorted tetrahedral coordination environments. The electronic properties such as HOMO and LUMO energies are carried out by gaseous phase DFT/B3LYP calculations using Gaussian 09 program. Complex 1 showed a good binding propensity to the DNA and HSA, during the assessment of docking studies. Schiff base ligand HL and its metal (II) complexes, 1–3 screened for their in vitro antimicrobial activities using the disc diffusion method against selected microbes. Complex 1 shows higher antimicrobial activity than complexes 2, 3 and Schiff base ligand HL. According to the results obtained from the cytotoxic studies, Schiff base ligand HL and its metal (II) complexes 1–3 have better cytotoxicity against MCF‐7 cell lines with potency higher than the currently used chemotherapeutic agent cyclophosphamide. 相似文献