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991.
调节硫酸氧钒与盐酸羟胺溶液至pH~4制得的题目晶体属空间群P2_1/n,晶胞参数a=8.201,b=8.597,c=9.947A,β=93.00°,Z=4.结构解出精修后R因子为0.069.结果表明,不对称单位中二个羟胺根以侧接态与VO~(3+)配位,另一羟胺取端接态以O占据V的第五赤道配位位置,配位水处于氧钒基强键反位,Cl~-则在配阳离子界外以平衡电荷,晶体对的化学式确证为[(VO~(3+))(NH_2O~_)_2(NH_3O)(H_2O)][Cl~-] 相似文献
992.
In this paper, we study the regularity of generalized solutions u(x,t) for the n -dimensional quasi-linear parabolic diffraction problem. By using various estimates and Steklov average methods, we prove that (1): for almost all t the first derivatives ux(x,t) are Hölder continuous with respect to x up to the inner boundary, on which the coefficients of the equation are allowed to be discontinuous; and (2): the first derivative ut(x,t) is Hölder continuous with respect to (x,t) across the inner boundary. 相似文献
993.
Mixed halide perovskites (MHPs) are a class of semiconductor materials with great promise for many optoelectronic applications due to their outstanding photophysical properties. Understanding and tailoring the photogenerated carrier dynamics is essential for further improvement of perovskite performance. Herein, we report a study about the carrier transport and interfacial charge transfer dynamics in Br-gradient MAPbI3-xBrx perovskite thin films prepared by surface ion-exchange method. Driven by the bandgap gradient in MAPbI3-xBrx films, the accelerated internal hole transport and enhanced interfacial extraction efficiency were both observed. Meanwhile, the interfacial electron transfer was also found to be evidently facilitated due to the surface modification during post-treatment. Our findings suggest the possibility of simultaneous acceleration of interfacial electron and hole transfer processes in halide perovskite films via surface post-treatment technique, which is of great importance in further improving the power conversion efficiency of perovskite solar cells. 相似文献
994.
Weihao Zeng Fanjie Xia Weixi Tian Fei Cao Junxin Chen Jinsong Wu Rongguo Song Shichun Mu 《Current Opinion in Electrochemistry》2022
The ever-increasing demand of advanced lithium-ion batteries is calling for high-performance cathode materials. Among promising next-generation cathode materials, high-nickel layered oxides with spherical polycrystalline secondary particles exhibit the outstanding advantage of high energy density. However, polycrystals, suffered from the pulverization of particles and the expansion of cracks, show the shortcoming of poor cycling performance. As an efficient solution, the single-crystal route has been underestimated hitherto. Herein, the unique structural degradation mechanism of single crystals is emphasized, and their advantages against polycrystals are comprehensively summarized in terms of electrochemical, thermal, and mechanical properties. Furthermore, we point out the practical challenges of single-crystal materials toward practical applications and raise hopeful strategies for overcoming such issues. Based on the aforementioned characteristics and approaches, future directions are outlooked as well. 相似文献
995.
Yong Leng Kelvin Tan 《Journal of organometallic chemistry》2007,692(11):2253-2269
The heteronuclear cluster RuOs3(μ-H)2(CO)13 (1) reacted readily with a number of ditertiary phosphines under chemical activation with trimethylamine-N-oxide. The solid-state and solution structures of these derivatives have been examined. Six structural types have been characterized crystallographically, including one in which a phenyl group migrates from the ditertiary phosphine ligand to the metal framework. There are many more isomers present in solution, most of which are rapidly inter-converting via hydride migrations. 相似文献
996.
The palladium-catalyzed tandem arylation of O-homoallylhydroxylamines with 2 equiv of aryl bromides was examined. With Pd2(dba)3 (1 mol %) as the catalyst, Xantphos (2 mol %) as the ligand, and NaOt-Bu as the base, the reactions of O-homoallylhydroxylamines with aryl bromides via sequential N-arylation/cyclization/C-arylation in toluene afforded the corresponding N-aryl-3-arylmethylisoxazolidines in good yields with excellent diastereoselectivity. 相似文献
997.
Beta-cyclodextrin and its permethylated derivatives form 2:1 inclusion complexes with tetrakis- and octakis(4-carboxyphenoxy)phthalocyanines 1-4, reducing their aggregation tendency and promoting their sensitization of singlet oxygen formation in aqueous media. 相似文献
998.
Single-walled carbon nanotubes binding to human telomeric i-motif DNA: significant acceleration of S1 nuclease cleavage rate 总被引:2,自引:0,他引:2
Single-walled carbon nanotubes (SWNTs) binding to human telomeric i-motif DNA can significantly accelerate S1 nuclease cleavage rate by increasing the enzyme turnover number. 相似文献
999.
The in vitro chemical stability and etching of ZnO nanostructures in simulated physiological solution (SPS) were studied using electron microscopy. Calcium hydrogen phosphate thin layers were observed to be uniformly deposited on the surfaces of ZnO nanomaterials in SPS. Electron diffraction and high-resolution transmission electron microscopy revealed that the calcium hydrogen phosphate layers were amorphous and had excellent interfacial contact with the nanocrystals. ZnO nanostructures fabricated by thermal evaporation were found to survive much longer in SPS than those fabricated using a hydrothermal solution method. The shapes of the voids formed in the ZnO nanostructures by the etching in SPS can be used to deduce the polar directions of ZnO nanostructures. 相似文献
1000.
Yanjie Zhang Lu Zhang Wenjie Wang Qingqing Deng Mengmeng Liu Zitong Zhu Hao Liu Prof. Jinsong Ren Prof. Xiaogang Qu 《Angewandte Chemie (International ed. in English)》2023,62(32):e202306395
Transition metal catalysts (TMCs) mediated bioorthogonal uncaging catalysis has sparked increasing interest in prodrug activation. However, due to their “always-on” catalytic activity as well as the complex and catalytic-detrimental intracellular environment, the biosafety and therapeutic efficiency of TMCs are unsatisfactory. Herein, a DNA-gated and self-protected bioorthogonal catalyst has been designed by modifying nanozyme-Pd0 with highly programmable nucleic acid (DNA) molecules to achieve efficient intracellular drug synthesis for cancer therapy. Monolayer DNA molecules could endow the catalyst with targeting and perform as a gatekeeper to achieve selective prodrug activation within cancer cells. Meanwhile, the prepared graphitic nitrogen-doped carbon nanozyme with glutathione peroxidase (GPx) and catalase (CAT)-like activities could improve the catalytic-detrimental intracellular environment to prevent the catalyst from being inactivated and sensitize the subsequent chemotherapy. Overall, we believe that our work will promote the development of secure and efficient bioorthogonal catalytic systems and provide new insights into novel antineoplastic platforms. 相似文献