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991.
A new photochromic diarylethene (1a) has been prepared. Both its photochromic behavior and nonlinear optical properties are
investigated. 1a shows excellent ring-opening (λmax = 386 nm) and ring-closing (λmax = 652 nm) photoisomerization with UV-Vis light irradiation. With 800 nm femtosecond pulsed laser irradiation, 1a shows two-photon-induced
photoisomerization, and a two-photon absorption cross-section (σ = 423×1050 cm4·s per photon) is obtained by using two-photon induced fluorescence method. The applications of two-photon absorption of 1a
to holographic recording has been also investigated. A two-photon induced micro-pattern is recorded on the diarylethene 1a-PMMA
film with an femtosecond laser of 800 nm, 100 fs, 1 kHz, 50 mW. 相似文献
992.
A new unsymmetrical photochromic diarylethene, namely1-[2-methyl-5-(p-N,N-dimethylaminophenyl)-3-thienyl]-2-[2-methyl-5-(3-methoxylphenyl)-3-thienyl]
perfluorocyclopentene (1a), was synthesized. The compound showed good photochromism, high sensitivity and remarkable fatigue-resistance
both in solution and in poly(methyl methacrylate) (PMMA) matrix with UV/Vis light irradiation. The absorption maximum of its
closed-ring isomer was observed at 624 nm in PMMA amorphous film. It is a nice match for the wavelength of the recording laser
(633 nm). Using this target compound as recording medium, four types of polarization holographic optical recordings were performed
successfully using a He-Ne laser. The results showed that only the orthogonal circular polarization recording could obtain
a hologram with high diffraction efficiency and high signal-to noise-ratio. With multiplexing recording technology, three
types of polarization multiplexing holographic optical recordings, including angular multiplexing, polarization multiplexing,
and angular plus polarization multiplexing holographic recording, were also carried out perfectly based on its photoinduced
anisotropic phenomenon accompanying the photochromic reaction by photoirradiation. The results demonstrate that the multiplexing
recording technology is an effective method to improve recording capacity when using diarylethene 1 as recording medium. 相似文献
993.
A high molecular weight aromatic homopoly(ester‐imide) (homoPEI) was synthesized from homopoly(ester‐amic acids) (homoPEAA), which was obtained from the reaction of bis(trimellitic acid anhydride) phenyl ester (BTAH) with 4‐4'‐oxydianiline ether (ODA). This homoPEI was melt‐processable semi‐crystalline polymer and displayed dual endothermic transitions which were attributed to the different levels of crystal perfection and size in the crystal structures. Four high molecular weight aromatic copoly(ester‐imide)s (coPEIs) were synthesized via copoly(ester‐amic acids)s (coPEAA) from the reaction of 4, 4'‐oxydiphthalic anhydride (ODPA) and BTAH with ODA. The molar percentage of BTAH varied from 10 to 40%. When the molar percentages of BTAH were 30 and 40%, the resulting two coPEIs were crystallinable and their melting temperatures were 361°C and 356/371°C, respectively. Differential scanning calorimetry (DSC) and wide angle X‐ray diffraction (WAXD) results indicated that the crystal structures included short segments of BTAH/ODA and ODPA/ODA. The initial crystallization of the two coPEIs took place during imidization process. Thermogravimetric (TA) and mechanical analysis confirmed that both homoPEI and coPEIs showed almost no weight loss until 400°C in N2 and good mechanical properties. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
994.
A colorimetric strategy based on conjugated polyelectrolyte aggregates has been applied to determine and distinguish anionic, cationic and non-ionic surfactants. 相似文献
995.
This paper reports the synthesis of a perylene-bridged bis(crown ether) through the condensation reaction between primary amine-armed dibenzo-24-crown-8 and 3,4,9,10-perylenetetracarboxylic dianhydride. Pseudorotaxane with a perylene moiety at the wheel and a fullerene unit in the middle of the axle was prepared, which was evidenced by 1H NMR and fluorescence experiments. Subsequent investigations show that the formation and disassociation of the pseudorotaxane can be controlled by the alternating addition of KPF6 and 18-crown-6, following the change of the florescence intensity of perylene.
相似文献996.
The syntheses and reactivity of the two N‐heterocyclic carbene (NHC)→ silylene complexes 2 and 4 have been investigated. The latter are easily accessible by reaction of the zwitterionic, N‐heterocyclic silylene LSi: 1 [L=Ar‐N‐C(=CH2)CH?C(Me)‐N‐Ar, Ar=2,6‐iPr2C6H3] with 1,3,4,5‐tetramethylimidazol‐2‐ylidene and 1,3‐diisopropyl‐4,5‐dimethylimidazol‐2‐ylidene, respectively. While compound 2 undergoes facile rearrangement above ?20 °C to give the unsymmetrical N‐heterocyclic silylcarbene 3 , the derivative 4 remains unchanged even after boiling in benzene. The remarkable reactivity of 3 and 4 towards cyclohexylisocyanide has been examined which leads in a unique series of C? H, Si? H, and C? N bond activations to the new triaminosilanes 5 and 6 , respectively. The novel compounds 3 , 4 , 5 , and 6 were fully characterized by 1H, 13C, and 29Si NMR spectroscopy, EI‐MS, elemental analysis, and single‐crystal X‐ray diffraction. 相似文献
997.
Polyurea-entrapped palladium nanoclusters have been prepared by interfacial polymerization in W/O emulsion and showed high thermal stability and chemical stability with the content of 0.12 mmol g?1 Pd. This catalyst exhibited dual catalytic activity for reduction of nitro compounds and hydrodehalogenation of aromatic chlorides in atmospheric hydrogen with 100% yield for reduction of nitro compounds and >99% yield for hydrodehalogenation of aromatic chlorides. This immobilizing method was particularly effective and eliminated the need of special chelating groups. 相似文献
998.
999.
采用微波辅助-液液微提取高效液相色谱法测定环境水样中的三嗪类除草剂.优化了提取溶剂的种类和体积、样品溶液的pH值、盐的浓度、提取时间、微波功率、振荡时间和离心速度等实验条件.在20 mL水样中,加入200 μL 1-己基-3-甲基咪唑六氟磷酸盐(提取剂),控制NaCl的含量为3%(m/V),在300 W时常压微波提取加热1 min,振荡15 min. 提取完成后,在冰水浴中冷却20 min后, 以8000 r/min离心5 min.在最佳实验条件下,5种除草剂在2.5~60 μg/L范围内线性良好,相关系数在0.9972~0.9991之间; 检出限为0.56~1.44 μg/L. 相似文献
1000.