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71.
Kihong Son Haijo Jung Sang Hun Shin Hyun-Ho Lee Mi-Sook Kim Young Hoon Ji Kum Bae Kim 《Radiation measurements》2011,46(10):1117-1122
We aimed to evaluate the suitability of a glass dosimeter (GD) for high-energy photon and electron beams in experimental and clinical use, especially for radiation therapy. We examined the expanded dosimetric characteristics of GDs including dose linearity up to 500 Gy, uniformity among GD lots and for individual GDs, the angular dependence, and energy dependence of 4 therapeutic x-ray qualities. In addition, we measured the dosimetric features (dose linearity, uniformity, angular dependence, and energy dependence) of the GD for electron beams of 10 different electron energy qualities. All measurements with the exception of dose linearity for photon beam were performed in a water phantom. For high-energy photon beams, dose linearity has a linear relationship for a dose ranging from 1 to 500 Gy with the coefficient of determination; R2 of 0.998. The uniformity of each GD of dose measurements was within ±0.5% for four GD lots and within ±1.2% for 80 GDs. In terms of the effects of photon beam angle, lower absorbed doses of within 1.0% were observed between 60° and 105° than at 90°. The GD energy dependence of 4 photon beam energy qualities was within ±2.0%. On the other hand, the result of the dose linearity for high-energy electron beams showed well fitted regression line with the coefficient of determination; R2 of 0.999 between 6 and 20 MeV. The uniformity of GDs exposed to the nominal electron energies 6, 9, 12, 16, and 20 MeV was ±1.2%. In terms of the angular dependence to electron beams, absorbed doses were within 2.0% between 60° and 105° than at 90°. In evaluation of the energy dependence of the GD at nominal electron energies between 5 and 20 MeV, we obtained responses between 1.1% and 3.5% lower than that for a cobalt-60 beam. Our results show that GDs can be used as a detector for determining doses when a high-energy photon beam is used, and that it also has considerable potential for dose measurement of high-energy electron beam. 相似文献
72.
Let X be a Banach space and L the generator of the evolution semigroup associated with the τ -periodic evolutionary process {U(t,s)}t≥s on the space Pτ(X) of all τ-periodic continuous X -valued functions. We give criteria for the existence of periodic solutions to nonlinear systems of the form Lp=−?F(p,?) under the condition that 1 is a normal eigenvalue of the monodromy operator U(τ,0). The proof is based on a new decomposition of the space Pτ(X) by constructing a right inverse of L. 相似文献
73.
Son‐Young Yi 《Numerical Methods for Partial Differential Equations》2014,30(4):1189-1210
In this article, we propose a mixed finite element method for the two‐dimensional Biot's consolidation model of poroelasticity. The new mixed formulation presented herein uses the total stress tensor and fluid flux as primary unknown variables as well as the displacement and pore pressure. This method is based on coupling two mixed finite element methods for each subproblem: the standard mixed finite element method for the flow subproblem and the Hellinger–Reissner formulation for the mechanical subproblem. Optimal a‐priori error estimates are proved for both semidiscrete and fully discrete problems when the Raviart–Thomas space for the flow problem and the Arnold–Winther space for the elasticity problem are used. In particular, optimality in the stress, displacement, and pressure has been proved in when the constrained‐specific storage coefficient is strictly positive and in the weaker norm when is nonnegative. We also present some of our numerical results.Copyright © 2014 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq 30: 1189–1210, 2014 相似文献
74.
Seon‐Kyoung Son Yoon‐Suk Choi Woo‐Hyung Lee Yongtaek Hong Jae‐Ryoung Kim Won‐Suk Shin Sang‐Jin Moon Do‐Hoon Hwang In‐Nam Kang 《Journal of polymer science. Part A, Polymer chemistry》2010,48(3):635-646
A series of new phenothiazylene vinylene‐based semiconducting polymers, poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene] ( P1 ), poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene‐alt‐1,4‐phenylene vinylene] ( P2 ), and poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene‐alt‐2,5‐thienylene vinylene] ( P3 ), have been synthesized via a Horner‐Emmons reaction. FTIR and 1H NMR spectroscopies confirmed that the configurations of the vinylene groups in the polymers were all‐trans (E). The weight‐averaged molecular weights (Mw) of P1 , P2 , and P3 were found to be 27,000, 22,000, and 29,000, with polydispersity indices of 1.91, 2.05, and 2.25, respectively. The thermograms for P1 , P2 , and P3 each contained only a broad glass transition, at 129, 167, and 155 °C, respectively, without the observation of melting features. UV–visible absorption spectra of the polymers showed two strong absorption bands in the ranges 315–370 nm and 450–500 nm, which arose from absorptions of the phenothiazine segments and the conjugated main chains. Solution‐processed field‐effect transistors fabricated from these polymers showed p‐type organic thin‐film transistor characteristics. The field‐effect mobilities of P1 , P2 , and P3 were measured to be 1.0 × 10?4, 3.6 × 10?5, and 1.0 × 10?3 cm2 V?1 s?1, respectively, and the on/off ratios were in the order of 102 for P1 and P2 , and 103 for P3 . Atomic force microscopy and X‐ray diffraction analysis of thin films of the polymers show that they have amorphous structures. A photovoltaic device in which a P3 /PC71BM (1/5) blend film was used as the active layer exhibited an open‐circuit voltage (VOC) of 0.42 V, a short circuit current (JSC) of 5.17 mA cm?2, a fill factor of 0.35, and a power conversion efficiency of 0.76% under AM 1.5 G (100 mW cm?2) illumination. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 635–646, 2010 相似文献
75.
76.
Kyung‐Sun Son Robert M. Waymouth 《Journal of polymer science. Part A, Polymer chemistry》2010,48(7):1579-1585
A series of monocyclopentadienyl titanium complexes containing a pendant amine donor on a Cp group ( A = CpTiCl3, B = CpNTiCl3, C = CpNTiCl2TEMPO, for Cp = C5H5, CpN = C5H4CH2CH2N(CH3)2, and TEMPO = 2,2,6,6‐tetramethylpiperidine‐N‐oxyl) are investigated for styrene homopolymerization and ethylene–styrene (ES) copolymerization. When activated by methylaluminoxane at 70 °C, complexes with the amine group ( B and C ) are active for styrene homopolymerization and afford syndiotactic polystyrene (sPS). The copolymerizations of ethylene and styrene with B and C yield high‐molecular weight ES copolymer, whereas complex A yields mixtures of sPS and polyethylene, revealing the critical role that the pendant amine has on the polymerization behavior of the complexes. Fractionation, NMR, and DSC analyses of the ES copolymers generated from B and C suggest that they contain sPS. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1579–1585, 2010 相似文献
77.
78.
In the asymptotically flat two-dimensional dilaton gravity, we present an N-body particle action which has a dilaton coupled mass term for the exact solubility. This gives nonperturbative exact solutions for the N-body self-gravitating system, so the infalling particles form a black hole and their trajectories are exactly described. In our two-dimensional case, the critical mass for the formation of black holes does not exist, so even a single particle forms a black hole. The infalling particles give additional time-like singularities in addition to the space-like black hole singularity. However, the latter singularities can be properly cloaked by the future horizons within some conditions. 相似文献
79.
We have synthesizedN-methyl-9-anthrylhydroxamic acid, which is a fluorescent analogue ofN-methylbenzohydroxamic acid. Complexation with various di- and trivalent metal ions occurs (logK from 4 to 5) in water with resulting fluorescence quenching. Because the Fe(III) and Al(III) complexes substituted rather slowly, the addition of EDTA provides a temporal method for obtaining some selectivity in the chemosensor. 相似文献
80.
Seung H. Son 《Journal of Number Theory》2006,121(1):114-117
Ramanujan recorded additive formulae of theta functions that are related to modular equations of degree five. We present elementary and simple proofs. 相似文献