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131.
132.
Abrams GS Adolphsen CE Aleksan R Alexander JP Averill D Ballam J Barish BC Barklow T Barnett BA Bartelt J Bethke S Blockus D de Boer W Bonvicini G Boyarski A Brabson B Breakstone A Brom JM Bulos F Burchat PR Burke DL Cence RJ Chapman J Chmeissani M Cords D Coupal DP Dauncey P DeStaebler HC Dorfan DE Dorfan JM Drell PS Drewer DC Elia R Fay J Feldman GJ Fernandes D Field RC Ford WT Fordham C Frey R Fujino D Gan KK Gero E Gidal G Glanzman T Goldhaber G Gomez Cadenas JJ Gratta G Grindhammer G 《Physical review letters》1989,63(15):1558-1561
133.
Abrams GS Adolphsen CE Averill D Ballam J Barish BC Barklow T Barnett BA Bartelt J Bethke S Blockus D Bonvicini G Boyarski A Brabson B Breakstone A Brom JM Bulos F Burchat PR Burke DL Cence RJ Chapman J Chmeissani M Cords D Coupal DP Dauncey P DeStaebler HC Dorfan DE Dorfan JM Drewer DC Elia R Feldman GJ Fernandes D Field RC Ford WT Fordham C Frey R Fujino D Gan KK Gero E Gidal G Glanzman T Goldhaber G Gomez Cadenas JJ Gratta G Grindhammer G Grosse-Wiesmann P Hanson G Harr R Harral B Harris FA 《Physical review letters》1989,63(20):2173-2176
134.
Abrams GS Adolphsen CE Aleksan R Alexander JP Allen MA Atwood WB Averill D Ballam J Bambade P Barish BC Barklow T Barnett BA Bartelt J Bethke S Blockus D de Boer W Bonvicini G Boyarski A Brabson B Breakstone A Breidenbach M Brom JM Brown JL Brown KL Bulos F Burchat PR Burke DL Cence RJ Chapman J Chmeissani M Clendenin J Cords D Coupal DP Dauncey P Dean NR DeStaebler HC Dorfan DE Dorfan JM Drell PS Drewer DC Dydak F Ecklund S Elia R Erickson RA Fay J Feldman GJ Fernandes D Field RC Fieguth TH 《Physical review letters》1989,63(7):724-727
135.
136.
Al-Smadi Mousa El-khateeb Mohammad Moriyama Hayato Yoshida Yukihiro Kitagawa Hiroshi 《Transition Metal Chemistry》2021,46(6):465-470
Transition Metal Chemistry - Reactions of (dppe)NiCl2 (dppe?=?1,2-bis(diphenylphosphino)ethane) with chlorido-substituted phenyl thiolates (RClS?) produced the corresponding... 相似文献
137.
This work reports synthesis and characterization of heterocyclic functionalized polymers, poly(triazole-etherimidazole)s(PTAEI), from a dialkyne-terminated compound, 3-(4,5-bis(4-(propargyloxy)phenyl)-1H-imidazol-2-yl)-9-ethyl-9H-carbazole, by using click reaction. PTAEIs were characterized and their properties such as solubility, thermal, mechanical, photophysical and metal ions adsorption were investigated. These polymers had weight average molar masses(Mw) in the range of 19100-26700 g/mol, exhibited excellent solubility in polar aprotic solvents and formed low-colored flexible thin films by solution casting method. They exhibited good thermal stability with glass transition temperatures(Tg) between 160 °C and 211 °C and 10% weight loss temperatures(T10%) in the range of 308-426 °C. Nanocomposites of PTAEIs with epoxide-terminated Fe3O4 showed that strong interfacial interaction between inorganic particles and the polymer matrix contributed to the enhanced thermal and mechanical properties. The photoluminescence intensity of the PTAEIs increased and the spectra red shifted with increasing Fe3O4 content. The PTAEIs and nanocomposites were tested for their extraction capability of metal ions from aqueous solutions either individually or in the mixture. 相似文献
138.
Kaolin-filled polypropylene (PP) composites with various kaolin content, processing temperature and shear histories were compounded
using a heated two roll-mill. Prior to thermal analysis, the samples were subjected to extrusion process via capillary rheometer.
The influences of kaolin content, processing temperature and shear stress on crystallization of all samples, including isothermal
and nonisothermal crystallization behaviour were investigated by differential scanning calorimetry (DSC). The results showed
that the increasing kaolin content, processing temperature and shear stress have shifted the crystallization exothermic peak
to higher temperature and reduced the overall crystallization time. 相似文献
139.
Michael E. Deary Salem M. Mousa D. Martin Davies 《Journal of inclusion phenomena and macrocyclic chemistry》2012,74(1-4):77-86
This paper presents a thermodynamic study of the rate and equilibria processes involved in the α-cyclodextrin mediated reaction of a range of 4-substituted phenyl methyl sulfides with two peroxyacids of different binding affinities. The results for the inclusion processes show that the formation of 1:1 and 2:1 (host:guest) complexes between α-cyclodextrin and phenyl methyl sulfides are generally enthalpically controlled, particularly so for the 2:1 complexes, as might be expected for a ternary complex. The data from this series of sulfides is presented as enthalpy-entropy compensation plots, yielding slopes of unity for each inclusion process. The formation of a 1:1 complex between cyclodextrin and the strongly associating 3-chloroperbenzoic acid (MCPBA) is also enthapically controlled. The other peroxyacid used, peroxomonosulfate, does not bind to α-cyclodextrin to any measurable degree. As described in our original study of this reaction system (Davies and Deary in J Chem Soc Perkin Trans 2:2423–2430, 1996), catalysis by α-cyclodextrin is effected by activation of the peroxide as a result its inclusion within the cyclodextrin cavity; hence for reactions of phenyl methyl sulfides with MCPBA, catalysis is observed, but is absent for PMS. In this study the reaction rates are analysed using the transition state pseudo-equilibrium approach of Tee (Carbohydr Res 192:181–195, 1989), whereby the transition state pseudoequilibrium constant K TS reflects the stabilisation imparted to the transition state by the association with one molecule of cyclodextrin. Enthalpy- entropy compensation plots for K TS give slopes close to unity; this is the first reported example of such plots being applied to transition state pseudoequilibrium constants. 相似文献
140.
Abdollah Omrani Mousa Ghaemy Abbas A. Rostami 《Journal of Thermal Analysis and Calorimetry》2009,98(2):477-483
The kinetics and mechanism of cure reaction of DGEBA using a chelate of Ni(II) with diethylenetriamine (dien), Ni(dien)2I2, as a curing agent was studied by DSC. TG curve of the complex curing agent showed mass loss in two region of temperature: 200–320 and 450–550 °C. Dynamic DSC measurements showed only one exothermic peak with a maximum about 250 °C depending on the heating rate. According to the methods of KAS and Ozawa–Flynn–Wall the values of E a were 92.5 and 96.2 kJ/mol, respectively. The isoconversional kinetic analysis in whole range of conversion, α = 0.02–0.95, showed small changes in the E a values in the region of α = 0.04–0.6 and most likely represent some average values (E a = 110 kJ/mol) between the values of E a of non-autocatalyzed and autocatalyzed reactions. Using the sole dependence of E a on α, the time required to reach fully cured materials under isothermal conditions were also predicted and compared with the experimental results. 相似文献