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排序方式: 共有358条查询结果,搜索用时 15 毫秒
1.
A single isomer of a monofunctionalised C70 fullerene is isolated and characterised using variable temperature NMR spectroscopy. Pendant methylene bromide groups allow for further cycloaddition reactions and a C60-C70 asymmetric fullerene dimer is thus prepared. 相似文献
2.
We describe the topology, structure, and stability of giant fullerenes exhibiting various symmetries (I, I
h
, D
2h
, T). Our results demonstrate that it is possible to create two new families of nested chiral icosahedral (I) fullerenes namely C260@C560@C980@C1520@, ...,and C140@C380@C740@C1220@ ..., which exhibit interlayer separations of ca. 3.4 Å. These chiral fullerenes are thought to possess metalliclike conduction properties. We discuss in detail the transformation of polyhedral graphitic particles into quasispherical nested giant fullerenes by reorganization of carbon atoms, which result in the formation of additional pentagonal and heptagonal carbon rings. These spherical structures are metastable and we believe they could be formed under extreme conditions, such as those produced by high-energy electron irradiation. There is circumstantial experimental evidence for the presence of heptagonal rings within these spherical fullerenes. 相似文献
3.
4.
5.
Lemi Türker 《Journal of Molecular Structure》2004,680(1-3):47-51
Semiempirical quantum chemical calculations at the level of AM1 (restricted Hartree–Fock) have been performed on a fullerene derivative, C54N4, theoretically obtained from C60 and its mono and diprotonated forms. All these structures are stable, but endothermic in nature. Some calculated geometrical and physicochemical properties of these have also been reported. 相似文献
6.
富勒烯掺杂有机光电导材料的光电导性 总被引:3,自引:0,他引:3
富勒烯掺杂有机光电导材料的光电导性徐铸德,陈万喜,冷拥军,许小平,李文铸(浙江大学化学系,物理系,杭州,310027)汪茫(浙江大学高分子科学与工程学系)关键词富勒烯,光化学,光物理,光电导体光电导材料在现代静电成像领域中有极广泛的应用,近年来,有机... 相似文献
7.
Orbital interaction analysis is employed to understand the complex charge transfer mechanism operative in endohedral metallofullerenes of composition NSc3@Cn (n = 68, 78). This phenomenon combines substantial electron transfer from the core to the cage with electron backdonation, involving the interaction between the occupied orbitals of the negatively charged cage and the unoccupied d orbitals of the positively charged core. This electron backdonation differs fundamentally from conventional orbital hybridization, which takes place primarily between the HOMO of the metal core and the LUMO of the fullerene cage. These findings imply the pronounced stability of NSc3@Cn (n = 68, 78), especially for NSc3 encapsulated in the non-IPR C68 enclosure, as experimentally established. 相似文献
8.
A novel method was proposed for the preparation of pyrenebutyric acid-modified magnesia-zirconia stationary phases. Pyrenebutyric acid was grafted to magnesia-zirconia composites with different pore sizes via the sodium salt of cis-(3-methyloxiranyl)phosphonic acid (fosfomycin) as spacers. Aminated fosfomycin was first absorbed onto the surface of magnesia-zirconia composites during the preliminary step to provide amino and hydroxy reactive sites. And then the pyrenebutyric acid was covalently attached to the amine or hydroxyl groups via amide or ester bonds. The resulting stationary phases were characterized by elemental analysis, diffused reflectance FT-IR, nitrogen adsorption analysis and 13C solid state NMR spectra. The HPLC separation of fullerenes on the new stationary phases with different pore sizes was also investigated. The chromatographic performance showed a dependence on the pore size of the magnesia-zirconia matrix. Little retention of fullerenes was observed on the stationary phase with pore sizes about 4.5 nm. However, on the modified magnesia-zirconia with pore sizes about 10 nm, selectivity factors (α) for C70/C60 separation were determined to be 1.76, 2.29, 2.41, 3.10, with carbon disulfide, chlorobenzene, xylene and toluene as mobile phases, respectively. And the high solubility of fullerenes in these solvents dramatically increased the overall potential with regard to preparative fullerene purification. Among the reported stationary phases with pyrene ligands, the pyrenebutyric acid-modified magnesia-zirconia (PYB-F-(ZrO2-MgO)) with larger pore sizes exhibited the best selectivity for fullerenes. The thermodynamic and kinetic behavior of fullerenes was also examined. 相似文献
9.
Timothy J. Hingston Kyriakos Porfyrakis G. Andrew D. Briggs 《Tetrahedron letters》2006,47(42):7413-7415
The synthesis of a short-chain fullerene dimer via bifunctional cycloaddition is demonstrated. A mono-functionalised C60 species is isolated, and has the potential for further organic functionalisation. 相似文献
10.
XUE Zhixin YANG Guipeng CHEN Dianbao MA Xiaomei ZHANG Xiqin QUAN Zhenlan 《反应性高分子(英文版)》2006,15(1):35-39
Fullerenes (C60/C70) linked up to Ni-doped ZnS through the medium of an amphalic polymer polyvinyl pyrrolidone (PVP) to form a new kind of photocatalyst for hydrogen evolution from aqueous Na2S/Na2SO3 solution under visible light irradiation, the photocatalytic activities of this novel photocatalyst C60/C70-PVP-Zn0.999Ni0.001S are 3-5 fold higher compared with that of precurse catalyst Zn0.999Ni0.001S. This result could be attributed to Schottky barrier layer built between C60/C70 and Zn0.999Ni0.001S due to the electro-negativity of C60 and characteristic of being used as a multiple electron acceptor. C60 or C60/C70, its moiety, with its low energy first excited singlet state, is a good energy acceptor and in addition readily accepts multiple electrons, making it a potential electron accumulate as we know, which could protect the separation between electrons and holes against combination. This is an important reason for the marked increase of amount of H2 evolution during the photocatalytic process for the composite system C60/C70-PVP-Zn0.999Ni0.001S. 相似文献