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101.
Supramolecular Phthalocyanine Assemblies for Improved Photoacoustic Imaging and Photothermal Therapy
Xingshu Li Eun‐Yeong Park Youngnam Kang Nahyun Kwon Mengyao Yang Seunghyun Lee Won Jong Kim Chulhong Kim Juyoung Yoon 《Angewandte Chemie (International ed. in English)》2020,59(22):8630-8634
Phototheranostic nanoplatforms are of particular interest for cancer diagnosis and imaging‐guided therapy. Herein, we develop a supramolecular approach to fabricate a nanostructured phototheranostic agent through the direct self‐assembly of two water‐soluble phthalocyanine derivatives, PcS4 and PcN4. The nature of the molecular recognition between PcS4 and PcN4 facilitates the formation of nanostructure (PcS4‐PcN4) and consequently enables the fabrication of PcS4‐PcN4 with completely quenched fluorescence and reduced singlet oxygen generation, leading to the high photoacoustic and photothermal activity of PcS4‐PcN4. In vivo evaluations suggest that PcS4‐PcN4 could not only efficiently visualize a tumor with high contrast through whole‐body photoacoustic imaging but also enable excellent photothermal therapy for cancer. 相似文献
102.
Kyeongnan Kwon 《Journal of Dispersion Science and Technology》2016,37(10):1518-1525
Glucose-responsive monoolein (MO) cubic phase was prepared by immobilizing proteinoid composed of Asp and Leu (PAL) and hydrophobically modified glucose oxidase (HmGOD) onto the MO bilayers. The hydrodynamic mean diameter of PAL aggregate in aqueous solution decreased with increasing the pH value. The number of pamitic acid residue per one molecule of HmGOD was determined to be 6.3 by a calorimetric method. HmGOD could acidify glucose solution in a few hours, possibly because it converted glucose to gluconic acid. PAL- and HmGOD-immobilized MO cubic phase was prepared by hydrating MO melt with the mixture aqueous solution of PAL and HmGOD. The cubic phase exhibited its phase transition around 62.5°C, determined by polarizing microscopy. The release of carboxylic fluorescein (CF) from the cubic phase was suppressed when the pH value of release medium decreased, possibly because PAL can aggregate more at a lower pH value. The release was suppressed when glucose concentration increased, possibly because the release medium can be more acidified and PAL will be more aggregated at a higher glucose concentration. The cubic phase could be used as a drug carrier which releases its content in a sustained manner when the glucose concentration is abnormally high. 相似文献
103.
Jae Hyung Park Yong Woo Cho Yoen Ju Son Kwangmeyung Kim Hesson Chung Seo Young Jeong Kuiwon Choi Chong Rae Park Rang-Woon Park In-San Kim Ick Chan Kwon 《Colloid and polymer science》2006,284(7):763-770
An anthracycline drug, adriamycin, was chemically conjugated onto the backbone of glycol chitosan via an acid-labile cis-aconityl linkage. The physicochemical characteristics of the glycol chitosan–adriamycin (GC–ADR) conjugates were investigated by dynamic light scattering, atomic force microscopy, and fluorescence spectroscopy. The GC–ADR conjugates were capable of forming nano-sized self-aggregates in an aqueous medium, when the adriamycin content in the conjugate was in the range of 2.0–5.0 wt.%. The self-aggregates were spherical in shape, and had mean diameters of 238–304 nm, depending on the adriamycin content. The critical aggregation concentrations of the conjugates, estimated by the fluorescence quenching method, were as low as 1.0–2.5×10−2 mg/ml. The size of self-aggregates was not affected by the polymer concentration in the range from 50 to 2,000 μg/ml, and was maintained up to 8 days in phosphate-buffered saline (pH 7.4), indicating high colloidal stability. The release of adriamycin from self-aggregates was significantly dependent on the pH of the medium due to the cis-aconityl linkage; e.g., the amount of adriamycin released for 4 days was 7.3±0.3% at pH 7, whereas it was 29.3±1.9% at pH 4. The cell viability results demonstrated that free adriamycin shows more potent cytotoxicity than the conjugates, primarily attributed to the sustained release of adriamycin from self-aggregates. In conclusion, the self-aggregates, formed by GC–ADR conjugates, might be useful for the site-specific delivery of adriamycin in a sustained manner. 相似文献
104.
The effect of a market factor on information flow between stocks using the minimal spanning tree 总被引:1,自引:0,他引:1
We empirically investigated the effects of market factors on the information flow created from N(N−1)/2 linkage relationships among stocks. We also examined the possibility of employing the minimal spanning tree (MST) method, which is capable of reducing the number of links to N−1. We determined that market factors carry important information value regarding information flow among stocks. Moreover, the information flow among stocks showed time-varying properties according to the changes in market status. In particular, we noted that the information flow increased dramatically during periods of market crises. Finally, we confirmed, via the MST method, that the information flow among stocks could be assessed effectively with the reduced linkage relationships among all links among stocks from the perspective of the overall market. 相似文献
105.
Alexander Efremov Youngkeun Kim Hyun-Woo Lee Kwang-Ho Kwon 《Plasma Chemistry and Plasma Processing》2011,31(2):259-271
The effects of HBr/Ar and HBr/Cl2 mixing ratios in the ranges of 0–100% Ar or Cl2 on plasma parameters, densities of active species influencing the dry etch mechanisms were analyzed at fixed total gas flow
rate of 40 sccm, total gas pressure of 6 mTorr, input power of 700 W and bias power of 300 W. The investigation combined plasma
diagnostics by Langmuir probes and the 0-dimensional plasma modeling. It was found that the dilution of HBr by Ar results
in maximum effect on the ion energy flux with expected impact on the etch rate in the ion-flux-limited etch regime, while
the addition of Cl2 influences mainly the relative fluxes of Br and Cl atoms on the etched surface with expected impact on the etch rate in the
reaction-rate-limited etch regime. 相似文献
106.
Min‐kyoung Ham Ji HoYouk Yong‐Ku Kwon Young‐Je Kwark 《Journal of polymer science. Part A, Polymer chemistry》2012,50(12):2389-2397
A photoinitiation process was investigated to develop a rapid and well‐controlled RAFT polymerization method applied to vinyl acetate (VAc) using methyl (ethoxycarbonothioyl)sulfanyl acetate (MESA) and bis(2,4,6‐trimethylbenzoyl)phenylphosphine oxide as the RAFT agent and photoinitiator, respectively. MESA was selected as the photochemically inert RAFT agent to minimize photolysis of the thiocarbonylthio groups during polymerization. Poly(vinyl acetate) with a prespecified well‐controlled molecular weight (MW) and a narrow MW distribution was successfully synthesized. The polymerization reaction proceeded as a living polymerization and was remarkably rapid compared with approaches that use thermally initiated processes with a very short induction period. A detailed kinetic study of the mechanism underlying the polymerization reaction, however, revealed that the chain ends containing xanthate moieties were not perfectly stable upon UV‐irradiation, and they generated radicals via homolytic cleavage. This reaction appeared to proceed by a combination of a degenerative transfer RAFT mechanism and a dissociation‐combination mechanism. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
107.
Sang Sub Kim Sun-Woo Choi Han Gil Na Dong Sub Kwak Yong Jung Kwon Hyoun Woo Kim 《Current Applied Physics》2013,13(3):526-532
ZnO–SnO2 branch–stem nanostructures were realized on a basis of a two-step process. In step 1, SnO2-stem nanowires were synthesized. In step 2, ZnO-branch nanowires were successfully grown on the SnO2-stem nanowires through a simple evaporation technique. We have pre-deposited thin Au layers on the surface of SnO2 nanowire stems and subsequently evaporated Zn powders on the nanowires. The ZnO branches, which sprouted from the SnO2 stems, had diameters in a range of 30–35 nm. As-synthesized branches were of single crystalline hexagonal ZnO structures. Since the branch tips were comprised of Au-containing nanoparticles, the Au-catalyzed vapor–liquid–solid growth mechanism was more likely to control the growth process of the ZnO branches. To test a potential use of ZnO–SnO2 branch–stem nanostructures in chemical gas sensors, their sensing performances with respect to NO2 gas were investigated, showing the promising potential in chemical gas sensors. 相似文献
108.
109.
Kwon BJ 《The Journal of the Acoustical Society of America》2002,112(2):634-641
Comodulation masking release (CMR) refers to an improvement in the detection threshold of a signal masked by noise with coherent amplitude fluctuation across frequency, as compared to noise without the envelope coherence. The present study tested whether such an advantage for signal detection would facilitate the identification of speech phonemes. Consonant identification of bandpass speech was measured under the following three masker conditions: (1) a single band of noise in the speech band ("on-frequency" masker); (2) two bands of noise, one in the on-frequency band and the other in the "flanking band," with coherence of temporal envelope fluctuation between the two bands (comodulation); and (3) two bands of noise (on-frequency band and flanking band), without the coherence of the envelopes (noncomodulation). A pilot experiment with a small number of consonant tokens was followed by the main experiment with 12 consonants and the following masking conditions: three frequency locations of the flanking band and two masker levels. Results showed that in all conditions, the comodulation condition provided higher identification scores than the noncomodulation condition, and the difference in score was 3.5% on average. No significant difference was observed between the on-frequency only condition and the comodulation condition, i.e., an "unmasking" effect by the addition of a comodulated flaking band was not observed. The positive effect of CMR on consonant recognition found in the present study endorses a "cued-listening" theory, rather than an envelope correlation theory, as a basis of CMR in a suprathreshold task. 相似文献
110.
We present a microscopic quantum theoretical analysis of the nanoscale superfluid properties of solvating clusters of para-H2 around the linear OCS molecule. Path-integral calculations with N=17 para-H2 molecules, constituting a full solvation shell, show the appearance of a significant superfluid response to rotation around the molecular axis at T=0.15 K. This low-temperature superfluid response is highly anisotropic and drops sharply as the temperature increases to T approximately 0.3 K. These calculations provide definitive theoretical evidence that an anisotropic superfluid state exists for molecular hydrogen in this microscopic solvation layer. 相似文献