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71.
A copper complex having quinoline moiety as fluorophore has been synthesized. The anion recognition behavior of the receptor and its copper complex has been studied in acetonitrile and in acetonitrile: H2O (95:5 v/v). The copper complex shows high selectivity toward acetate over other anions studied such as F−, Cl−, Br−, I−, OAc−, dl-malate, l-mandelate, benzoate, isophthalate, , and . 相似文献
72.
Formic and acetic acids are ubiquitous in the environment, food, and most of the natural products. Extraction of the acids from aqueous solution is required for their isotope analysis by the gas chromatography-isotope ratio mass spectrometry. To this objective, we have previously developed a purge-and-trap technique using the dynamic solid-phase microextraction technology, the NeedlEX. The extraction efficiency, however, remains unexamined. Here, we address this question using the flame ionization detector and isotope ratio mass spectrometer while comparing it with that of the CAR/PDMS fiber. The results show that the NeedlEX is applicable at a wide range of concentration through coordination of purge volume given the minimum amount 3.7 ng and 1.8 ng of formic and acetic, respectively, is extracted. The efficiency of NeedlEX was 6-7 times lower than the fiber at 1000 μg/mL depending on the analyte. It is, however, superior to the latter at 10 μg/mL or less owing to its lower detection limit. The extraction efficiency of both acids is equivalent in molar amount. This is, however, disguised by the different response of the flame ionization detector. The isotope ratio mass spectrometor overcomes this problem but is compromised by relatively large errors. These results are particularly useful for isotopic analysis of carboxylic acids. 相似文献
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Hydrothermal synthesis has afforded a pair of divalent copper acetate coordination polymers containing either 4, 4′‐dipyridylamine (dpa) or 4‐pyridylisonicotinamide (4‐pina), both of which hydrogen‐bonding capable central functional groups. X‐ray crystallography revealed that both exhibit a 1D chain dimensionality. Use of the kinked tethering ligand dpa produced [Cu(OAc)2(dpa)]n ( 1 ), which possesses a simple chain based on dpa linkage of isolated copper ions. On the other hand, employing the straighter amide ligand 4‐pina generated {[Cu(OAc)2(4‐pina)] · 0.5H2O}n ( 2 ), which exhibits {Cu2O2} rhomboid dimers formed through bridging acetate ligands. Weak antiferromagnetic coupling [g = 1.984(3), J = –3.2(3) cm–1] was observed within the axial‐equatorial bridged {Cu2O2} dimers in 2 , with possible ferrimagnetism due to spin canting below 11 K. 相似文献
76.
A simple Hg2+-selective chemodosimetric system based on thiosemicarbazone was investigated. The transformation of thiosemicarbazone into semicarbazone selectively exerted by Hg2+ ions and the dimerization of semicarbazone resulted in a pronounced OFF–ON-type fluorescent signaling behavior. The coexistent metal ions, such as Fe3+, Ca2+, Cu2+, Co2+, Ni2+, Cd2+, Pb2+, Zn2+, Cr3+, Mg2+, Na+, K+, and Fe2+, had no obvious interference with the detection of Hg2+. In addition, S12–Hg2+ plays a high sensitivity for basic anions to form an ‘OFF–ON–OFF’ type signaling behavior, with the Hg2+-induced emission spectra can be quenched. Moreover, test strips based on S12 exhibited a good selectivity to Hg2+. We believe the test strips could act as a convenient and efficient Hg2+ test kit. 相似文献
77.
J.W. John Bosco 《Tetrahedron letters》2006,47(24):4065-4068
Molecular iodine is found to catalyze the acetylation of alcohols efficiently with vinyl acetate. The reaction is mild and selective with good to high yields. Molecular iodine displays significant functional group tolerance, being compatible with methoxy, double bonds, spiroketals, ketals and phenolic hydroxyl functions. 相似文献
78.
Isothermal decomposition of un-irradiated and pre- n -irradiated dysprosium acetate [Dy(CH3COO)3] has been investigated at different temperatures between 603-623 v K. Irradiation was observed to enhance the rate of decomposition without modifying the mechanism of the thermal decomposition. Thermal decomposition of dysposium acetate is shown to proceed by a nucleation and growth mechanism (Avarmi-Erofe'ev equation) both for un-irradiated and pre- n -irradiated samples. The enhancement of the decomposition was found to increase with an increase in the n -ray dose applied to the sample and may be attributed to an increase in point defects and formation of additional nucleation centers generated in the host lattice. Thermodynamic values of the main decomposition process were calculated and evaluated. 相似文献
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Isabel García-Santos Jesús Sanmartín Ana M. García-Deibe Matilde Fondo Esther Gmez 《Polyhedron》2009,28(14):3055-3059
A linear trinuclear zinc complex was obtained when after refluxing 8-hydroxyquinoline-2-carboxaldehyde and 2-aminoethanol (in a 1:1 molar ratio) until the formation of the H2L ligand, a methanol solution of zinc acetate dihydrate was added. Reaction between Zn(OAc)2·2H2O and H2L, both in 3:2 or 4:2 ratios, yielded Zn3(HL)2(OAc)4. This latter could be crystallographically characterised, and rather surprisingly, the potentially tetradentate HL− is only acting as an O,N-donor, while two phenolate and four acetate bridges hold together the three zinc ions. A study of the luminescence properties in methanol solution showed that the quantum yield of Zn3(HL)2(OAc)4 (ΦF = 0.07) is slightly higher than that of 8-hydroxyquinoline-2-carboxaldehyde (ΦF = 0.06). 相似文献