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991.
Hong‐Cheu Lin Meng‐Dan Jiang Shen‐Chang Wu Leng‐Long Jou Kai‐Pin Chou Ching‐Mao Huang Kung‐Hwa Wei 《Journal of polymer science. Part A, Polymer chemistry》2009,47(18):4685-4702
A series of diblock‐copolymers were synthesized through anionic polymerization of styrene and tert‐butyl methacrylate (tBuA) with different monomer ratios, and analogous block‐copolymeric derivatives (PS‐b‐PAA)s with monofunctional carboxylic acid groups were obtained by further hydrolyzation as hydrogen‐bonded (H‐bonded) proton donors. Via H‐bonded interaction, these diblock‐coplymeric donors (PS‐b‐PAA)s were incorporated with luminescent mono‐pyridyl/bis‐pyridyl acceptors to form single/double H‐bonded supramolecules, that is, H‐bonded side‐chain/cross‐linking copolymers, respectively. The supramolecular architectures formed by donor polymers and light‐emitting acceptors were influenced by the ratio of acid blocks in the diblock copolymeric donors and the type of single/double H‐bonded light‐emitting acceptors. Their thermal and luminescent properties can be adjusted by H‐bonds, and more than 100 nm of red‐shifted photoluminescence (PL) emissions were observed, which depend on the degrees of the H‐bonding interactions. Self‐assembled phenomena of amphiphilic dibolck copolymers and their H‐bonded complexes were confirmed by TEM micrographs, and supramolecular microphase separation of spherical micelle‐like morphology was demonstrated to affect the photophysical properties. Polymer light‐emitting diode (PLED) devices containing H‐bonded complexes showed electroluminescence (EL) emissions of 503–560 nm under turn‐on voltages of 7.5–9.0 V, maximum power efficiencies of 0.23–0.37 cd/A (at 100 mA/cm2), and maximum luminances of 318–519 cd/m2 (around 25 V). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4685–4702, 2009 相似文献
992.
This article presents a simplicial branch and duality bound algorithm for globally solving the sum of convex–convex ratios problem with nonconvex feasible region. To our knowledge, little progress has been made for globally solving this problem so far. The algorithm uses a branch and bound scheme where the Lagrange duality theory is used to obtain the lower bounds. As a result, the lower-bounding subproblems during the algorithm search are all ordinary linear programs that can be solved very efficiently. It has been proved that the algorithm possesses global convergence. Finally, the numerical experiments are given to show the feasibility of the proposed algorithm. 相似文献
993.
A convenient route for the synthesis of 3,4-dihydrocoumarin derivates from salicylaldehyde derivates and 1,3-dicarbonyl compounds under solvent-free microwave irradiation conditions was described. In this way, a range of compounds was obtained in moderate to good yields in a short reaction time. 相似文献
994.
Feng Chen Weipu Zhu Ning Xu Zhiquan Shen 《Journal of polymer science. Part A, Polymer chemistry》2008,46(12):4050-4055
The ring‐opening copolymerization of ethylene carbonate (EC) with ε‐caprolactone (CL) was carried out using neodymium tris(2,6‐di‐tert‐butyl‐4‐methylphenolate) as a single‐component catalyst. Copolymers containing up to 22.0% EC contents with high molecular weights (up to 23.97 × 104) and moderate molecular weight distributions (between 1.66 and 2.03) were synthesized at room temperature. Compared with homopoly(ε‐caprolactone), the copolymers with EC units exhibited increased glass transition temperatures (?35.6 °C), reduced melting temperatures (44.5 °C), and greatly enhanced elongation percentage at break (2383%) based on dynamic mechanic analysis. The crystallinities of the copolymers decreased with the increasing EC molar percentage in the products. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4050–4055, 2008 相似文献
995.
Improvement of Steroid Biotransformation with Hydroxypropyl-β-Cyclodextrin Induced Complexation 总被引:1,自引:0,他引:1
Liting Zhang Min Wang Yanbing Shen Yinhu Ma Jianmei Luo 《Applied biochemistry and biotechnology》2009,159(3):642-654
The inclusion complexes induced by cyclodextrins and its derivates have been shown previously to enhance the biotransformation
of hydrophobic compounds. Using hydroxypropyl-β-cyclodextrin (HP-β-CD; 20% w/v), the water solubility of cortisone acetate increased from 0.039 to 7.382 g L−1 at 32 °C. The solubilization effect of HP-β-CD was far superior to dimethylformamide (DMF) and ethanol. The dissolution rate
also significantly increased in the presence of HP-β-CD. The enzymatic stability of Δ1-dehydrogenase from Arthrobacter simplex TCCC 11037 was not influenced by the increasing concentrations of HP-β-CD contrary to the organic cosolvents which negatively
influenced in the order DMF > ethanol. The activity inhibition effect caused by HP-β-CD was not so conspicuous as ethanol
and DMF. Inactivation constants of ethanol, DMF, and HP-β-CD were 5.832, 4.541, and 1.216, respectively. The inactivation
energy (E
a) was in the order of HP-β-CD (55.1 kJ mol−1) > ethanol (39.9 kJ mol−1) > DMF (37.1 kJ mol−1). 相似文献
996.
997.
998.
Peng‐Fei Gou Wei‐Pu Zhu Ning Xu Zhi‐Quan Shen 《Journal of polymer science. Part A, Polymer chemistry》2009,47(24):6962-6976
Well‐defined drug‐conjugated amphiphilic A2B2 miktoarm star copolymers [(PCL)2‐(PEG)2‐D] were prepared by the combination of controlled ring‐opening polymerization (CROP) and “click” reaction strategy. First, bromide functionalized poly(ε‐caprolactone) (PCL‐Br) with double hydroxyl end groups was synthesized by the CROP of ε‐caprolactone using 2,2‐bis(bromomethyl)propane‐1,3‐diol as a difunctional initiator in the presence of Sn(Oct)2 at 110 °C. Next, the bromide groups of PCL‐Br were quantitatively converted to azide form by NaN3 to give PCL‐N3. Subsequently, the end hydroxyl groups of PCL‐N3 were capped with ibuprofen as a model drug at room temperature. Finally, copper(I)‐catalyzed cycloaddition reaction between ibuprofen‐conjugated PCL‐N3 and slightly excess alkyne‐terminated poly(ethylene glycol) (A‐PEG) led to ibuprofen‐conjugated A2B2 miktoarm star copolymer [(PCL)2‐(PEG)2‐D]. The excess A‐PEG was removed by dialysis. 1H NMR, FTIR and SEC analyzes confirmed the expected miktoarm star architecture. These amphiphilic miktoarm star copolymers could self‐assemble into multimorphological aggregates in aqueous solution, which were characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). In addition, the drug‐loading capacity of these drug‐conjugated miktoarm star copolymers as well as their nondrug‐conjugated analogs were also investigated in detail. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009 相似文献
999.
1000.