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1.
The electrolytic sensor described is based on the oxidation of nitrite at a platinum electrode modified with chemisorbed iodine and coated with a thin layer of quaternized poly(4-vinylpyridine), qPVP. The sealed sensor uses an anion-exchange membrane to separate Donnan transport of nitrite across the membrane and controlled potential electrolysis at the Pt/qPVP indicator electrode. The sensor has a linear response to nitrate concentration in aqueous samples over the range 4 × 10?6?2 × 10?3 M nitrite. The detection limit is 2 × 10?6 M nitrite. The sensor is free of interference by nitrate, dissolved oxygen, cations, and many neutral species. Anions that are electroactive at 0.7 V vs. Ag/ AgCl would interfere, but they are uncommon in most samples. Initial tests with lake water samples suggest that this sensor is unaffected by this matrix. The system was also evaluated for monitoring nitrite levels in spiked meat extracts. 相似文献
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Martinez-Diaz MV Rodriguez-Morgade MS Feiters MC van Kan PJ Nolte RJ Stoddart JF Torres T 《Organic letters》2000,2(8):1057-1060
[formula: see text] New unsymmetrically substituted DB24C8-phthalocyanines, which are able to form complexes with suitable dialkylammonium cations, have been prepared. These complexes most probably have a pseudorotaxane geometry. 相似文献
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The intramolecular and long-range ferromagnetic coupling between p-phenylenediamine radical cations in head-to-tail coupled oligo(1, 4-phenyleneethynylene)s and oligo(1,4-phenylenvinylene)s between neighbors and next-nearest neighbors is described. UV/vis/near-IR experiments show that the radical cations are localized in the pendant p-phenylenediamine units of the conjugated oligomers. The ESR spectra of these oligo(1,4-phenyleneethynylene) and oligo(1, 4-phenylenvinylene) di(radical cation)s are consistent with those of a triplet state. A linear behavior is observed for the doubly integrated ESR intensity of the DeltaM(s) = +/-1 and DeltaM(s) = +/-2 signals with the inverse temperature (I approximately 1/T), consistent with Curie's law. This behavior indicates a triplet ground-state diradical with a large triplet-singlet energy gap or possibly a degeneracy of singlet and triplet states. 相似文献
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Pawel J. Kulesza Silvia Zamponi Marcin A. Malik Krzysztof Miecznikowski Mario Berrettoni Roberto Marassi 《Journal of Solid State Electrochemistry》1997,1(1):88-93
Using Prussian blue (PB) electrodeposited on gold-covered foil as a model system, we have demonstrated the usefulness of
the time-derivative measurements of absorbance versus potential (linear potential-scan voltabsorptometry) for spectroelectrochemical
characterization of thin electrochromic films. The time-derivative signals were monitored for PB at 680 and 420 nm in potassium,
sodium and lithium electrolytes. Information obtained from cyclic voltabsorptometry is equivalent or complementary to that
from conventional cyclic voltammetry. In the case of PB films investigated in lithium electrolyte, the voltabsorptometric
time-derivative peaks are better defined than the respective voltammetric peaks. The combination of voltabsorptometry with
voltammetry enables molar absorptivity and/or film loading to be determined. Also, concentration changes of differently colored
mixed-valence redox centers can be monitored as a function of applied potential.
Received: 16 January 1997 / Accepted: 11 March 1997 相似文献
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Stanisaw Porejko Wodzimierz Gabara Janina Kulesza 《Journal of polymer science. Part A, Polymer chemistry》1967,5(7):1563-1571
Grafting of maleic anhydride on polyethylene is found to take place also in a homogeneous medium. The course of reaction in nitrogen and in air and the influence of temperature of initiator and polymer concentrations suggest that grafting is due to the chain transfer reaction to polyethylene. 相似文献