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91.
This paper discusses the warp and accompanying residual stress in a rectangular epoxy beam produced by water cooling its lower surface. First, the theoretical values of this warp and residual stress are obtained by the linear-viscoelastic theory. The specimen is then subjected to quenching. The variations in the warp are observed. After quenching, the residual stress is measured by a layer-removal method. The experimental and theoretical results are then compared and discussed. 相似文献
92.
Minakata K Nozawa H Gonmori K Yamagishi I Suzuki M Hasegawa K Watanabe K Suzuki O 《Analytical and bioanalytical chemistry》2011,400(7):1945-1951
An electrospray ionization tandem mass spectrometric (ESI-MS-MS) method has been developed for the determination of cyanide
(CN–) in blood. Five microliters of blood was hemolyzed with 50 μL of water, then 5 μL of 1 M tetramethylammonium hydroxide solution
was added to raise the pH of the hemolysate and to liberate CN– from methemoglobin. CN– was then reacted with NaAuCl4 to produce dicyanogold, Au(CN)2–, that was extracted with 75 μL of methyl isobutyl ketone. Ten microliters of the extract was injected directly into an ESI-MS-MS
instrument and quantification of CN– was performed by selected reaction monitoring of the product ion CN– at m/z 26, derived from the precursor ion Au(CN)2– at m/z 249. CN– could be measured in the quantification range of 2.60 to 260 μg/L with the limit of detection at 0.56 μg/L in blood. This
method was applied to the analysis of clinical samples and the concentrations of CN– in the blood were as follows: 7.13 ± 2.41 μg/L for six healthy non-smokers, 3.08 ± 1.12 μg/L for six CO gas victims, 730 ± 867 μg
for 21 house fire victims, and 3,030 ± 97 μg/L for a victim who ingested NaCN. The increase of CN– in the blood of a victim who ingested NaN3 was confirmed using MS-MS for the first time, and the concentrations of CN– in the blood, gastric content and urine were 78.5 ± 5.5, 11.8 ± 0.5, and 11.4 ± 0.8 μg/L, respectively. 相似文献
93.
Contamination of the exterior surface of vials of cytostatic drugs by the drugs themselves is a potential hazard to human health. This study developed a validated method using liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) for the determination of contamination of the exteriors of vials of cisplatin and carboplatin. Large Alpha® sampling swabs were employed to wipe the vial exterior. Cisplatin or carboplatin and gold(III) as an internal standard were derivatized by N,N-diethyldithiocarbamate (DDTC). Pt(DDTC)3+ and Au(DDTC)2+ were monitored by the respective transitions of m/z 639.3-490.9 and 493.0-345.0, respectively. Each separation was completed within 9 min using a 3 μm particle ODS-column. Calibration curves for cisplatin and carboplatin were linear over concentration ranges of 30-10,000 and 30-30,000 pg vial−1, respectively. The accuracies and precisions were 96.1-102.5% and within 8.2% for intra-assay and 99.6-103.3% and within 7.6% for inter-assay, respectively. Their lower limit of quantification was 30 pg vial−1. Amounts of 0.17-17.0 ng vial−1 as cisplatin and 0.48-794 ng vial−1 as carboplatin were detected from the exterior surface of the vials. This validated method using LC-ESI-MS/MS for the determination of platinum anticancer drugs is helpful for monitoring contamination of the exterior surface of drug vials. 相似文献
94.
Novel thermally crosslinkable fluorine‐containing poly(arylene ether ketone)s comprised of 2,3,5, 6‐tetrafluoro‐1,4‐phenylene moiety were synthesized by the termination of polymer chain ends with propargyl ether groups in order to improve solvent resistance. Crosslinking reaction occurred over 250°C through the formation of both chromen ring and polyene structure. This structure change brought about not only the outstanding solvent resistance but also the increase in glass transition temperature (Tg). The cured films also exhibited excellent thermal stability, transparency and hydrophobicity derived from fluorine atoms. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
95.
Seiichi Takano Minoru Moriya Takashi Kamikubo Kou Hiroya Kunio Ogasawara 《Tetrahedron letters》1993,34(52):8485-8488
It has been revealed that the generation of 2-cyclohexenones from cis-1,4-dihydroxycyclohexene derivatives under PdCl2(PPh3)2-HCO2NH4 system takes place in an intramolecular pathway involving unprecedented mode of suprafacial 1,4-hydrogen migration across the 1,4-allylic centers. 相似文献
96.
Masanori Taruki Takeshi Wakui Isoshi Nukatsuka Kunio Ohzeki 《Analytical sciences》2007,23(12):1435-1438
A resin-phase extraction method has been optimized for the trace determination of tin(II) by ETAAS. Tin(II) was extracted on a finely divided anion exchange resin as the complex with ammonium pyrrolidinedithiocarbamate (APDC). The resin was collected on a membrane filter and then dispersed in 1.00 ml of 1 mol l(-1) nitric acid containing 100 microg of Pd(II) and 60 microg of Ni(II). The resulting resin suspension was subjected to GFAAS. The proposed method was applied to the determination of tin(II) in hydrochloric acid. 相似文献
97.
Shin‐ichiro Kohama Kunio Kimura Yuhiko Yamashita 《Journal of polymer science. Part A, Polymer chemistry》2005,43(9):1757-1766
Nonstoichiometric polycondensation of 4‐acetoxybenzoic acid (ABA) was examined in the presence of three kinds of aromatic monoacetates: 4‐hexyloxyphenyl acetate, 4‐decyloxyphenyl acetate, and 4‐octadecyloxyphenyl acetate. Polymerizations were carried out in liquid paraffin at 320 °C under nonstoichiometric conditions, in which the acetoxy group was in large excess of the carboxyl group. Poly(4‐oxybenzoyl) (POB) was obtained as crystal at the molar ratio of monoacetates in feed (χ) of less than 80 mol %, meaning that the concentration of the acetoxy group was five times that of the carboxylic group. The obtained POB possessed much higher number average degree of polymerization (DPn), ranging from 353 to 467, than the calculated DPn on the basis of χ. High molecular weight polymer was synthesized even under nonstoichiometric conditions via crystallization of oligomers and the following solid‐state polymerization in the crystals. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1757–1766, 2005 相似文献
98.
99.
100.
In contrast to previous reports e?t in 3MHx produced at 4 K shows trap relaxation when warmed to 77 K. The relaxation in 3 MHx and 3MP occurs without loss of e?t, and results in an increase in ?max as well as a shift of λmax. 相似文献