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91.
Self‐Assembly of a Giant Tetrahedral 3 d–4 f Single‐Molecule Magnet within a Polyoxometalate System
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Dr. Masooma Ibrahim Dr. Valeriu Mereacre Dr. Nicolas Leblanc Prof. Wolfgang Wernsdorfer Dr. Christopher E. Anson Prof. Annie K. Powell 《Angewandte Chemie (International ed. in English)》2015,54(51):15574-15578
A giant tetrahedral heterometallic polyoxometalate (POM) [Dy30Co8Ge12W108O408(OH)42(OH2)30]56?, which shows single‐molecule magnet (SMM) behavior, is described. This hybrid contains the largest number of 4f ions of any polyoxometalate (POM) reported to date and is the first to incorporate two different 3d–4f and 4f coordination cluster assemblies within same POM framework. 相似文献
92.
Methane as a Selectivity Booster in the Arc‐Discharge Synthesis of Endohedral Fullerenes: Selective Synthesis of the Single‐Molecule Magnet Dy2TiC@C80 and Its Congener Dy2TiC2@C80
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Katrin Junghans Christin Schlesier Aram Kostanyan Nataliya A. Samoylova Qingming Deng Marco Rosenkranz Sandra Schiemenz Dr. Rasmus Westerström Prof. Dr. Thomas Greber Prof. Dr. Bernd Büchner Dr. Alexey A. Popov 《Angewandte Chemie (International ed. in English)》2015,54(45):13411-13415
The use of methane as a reactive gas dramatically increases the selectivity of the arc‐discharge synthesis of M‐Ti‐carbide clusterfullerenes (M=Y, Nd, Gd, Dy, Er, Lu). Optimization of the process parameters allows the synthesis of Dy2TiC@C80‐I and its facile isolation in a single chromatographic step. A new type of cluster with an endohedral acetylide unit, M2TiC2@C80, is discovered along with the second isomer of M2TiC@C80. Dy2TiC@C80‐(I,II) and Dy2TiC2@C80‐I are shown to be single‐molecule magnets (SMM), but the presence of the second carbon atom in the cluster Dy2TiC2@C80 leads to substantially poorer SMM properties. 相似文献
93.
Three unprecedented nitronyl nitroxide radical‐bridged 3d–4f clusters, [Ln2Cu2(hfac)10(NIT‐3py)2(H2O)2](LnIII=Y, Gd, Dy), have been obtained from the self‐assembly of Ln(hfac)3, Cu(hfac)2, and the radical ligand. The Dy complex shows a slow relaxation of magnetization, representing the first nitronyl nitroxide radical‐based 3d–4f cluster with single‐molecule magnet behavior. 相似文献
94.
M. Sc. Mukesh Kumar Singh Prof. Gopalan Rajaraman 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(3):980-983
This theoretical study suggests that CH???π stacking interactions between monomeric units can be used to design novel single‐chain magnets (SCMs), as the sign of coupling is predictable and such chains inherently yield negative axial anisotropy, a condition often difficult to achieve in conventional SCMs. 相似文献
95.
Lanthanide Complexes with Multidentate Oxime Ligands as Single‐Molecule Magnets and Atmospheric Carbon Dioxide Fixation Systems
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Dr. Małgorzata Hołyńska Dr. Rodolphe Clérac Mathieu Rouzières 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(38):13321-13329
The synthesis, structure, and magnetic properties of five lanthanide complexes with multidentate oxime ligands are described. Complexes 1 and 2 ( 1 : [La2(pop)2(acac)4(CH3OH)], 2 : [Dy2(pop)(acac)5]) are synthesized from the 2‐hydroxyimino‐N‐[1‐(2‐pyridyl)ethylidene]propanohydrazone (Hpop) ligand, while 3 , 4 , and 5 ( 3 : [Dy2(naphthsaoH)2(acac)4H(OH)]?0.85 CH3CN?1.58 H2O; 4 : [Tb2(naphthsaoH)2(acac)4H(OH)]?0.52 CH3CN?1.71 H2O; 5 : [La6(CO3)2(naphthsao)5 (naphthsaoH)0.5(acac)8(CO3)0.5(CH3OH)2.76H5.5(H2O)1.24]?2.39 CH3CN?0.12 H2O) contain 1‐(1‐hydroxynaphthalen‐2‐yl)‐ethanone oxime (naphthsaoH2). In 1 – 4 , dinuclear [Ln2] complexes crystallize, whereas hexanuclear LaIII complex 5 is formed after fixation of atmospheric carbon dioxide. DyIII‐based complexes 2 and 3 display single‐molecule‐magnet properties with energy barriers of 27 and 98 K, respectively. The presence of a broad and unsymmetrical relaxation mode observed in the ac susceptibility data for 3 suggest two different dynamics of the magnetization which might be a consequence of independent relaxation processes of the two different Dy3+ ions. 相似文献
96.
《化学:亚洲杂志》2017,12(21):2772-2779
Single‐molecule magnets (SMMs) exhibiting slow relaxation of magnetization of purely molecular origin are highly attractive owing to their potential applications in spintronic devices, high‐density information storage, and quantum computing. In particular, lanthanide SMMs have been playing a major role in the advancement of this field because of the large intrinsic magnetic anisotropy of lanthanide metal ions. Herein, some recent breakthroughs that are changing the perspective of the field are highlighted, with special emphasis on synthetic strategies towards the design of high‐performance SMMs. 相似文献
97.
The paper presents a theoretical and experimental study of vibrating structures where paramagnetic or diamagnetic systems interact with rare-earth passive magnets.The theoretical model of the system is focused on the damping properties of permanent magnets and on their interactions with the dynamic behaviour of an Euler–Bernoulli beam. In particular, the magnetic model is based on the analogy of the equivalent currents method in a quasi-static open-circuit-type configuration and it is used to determine the influence of eddy currents on the dynamic behaviour of conducting material structures. The magnetic effects are characterised by a viscous-type damping and by a stiffening dynamic effect of the structure, called “phantom effect”.The authors present the experimental outcomes for uniform cantilever clamped-free beams of different kinds of paramagnetic or diamagnetic conducting materials. It appears that the system frequency response can be modified by the presence of a pair of concordant or discordant permanent magnets of high residual induction settled at the free end.Through the comparison between theoretical and experimental results, the paper demonstrates the validity of the model, that is able to describe both the above mentioned effect of dynamic stiffening of the structure and the considerable localised damping properties in paramagnetic or diamagnetic materials having low electric resistivity. 相似文献
98.
Nicola Magnani 《International journal of quantum chemistry》2014,114(12):755-759
Magnetic exchange is an essential feature of transition‐metal nanomagnets because it combines the relatively low spin‐only moments of several ions into a “giant spin” ground state, which can make slow magnetic relaxation very favorable in an axially anisotropic environment. In contrast, most of the early research on lanthanide‐based complexes focused on single‐ion magnets, where the required large moment is generated by the unquenched orbital contribution (which is parallel to the spin in heavy rare earths). With their unfilled 5f electronic shell being on the verge between localization and itinerancy, actinides are expected to combine the best of both 3d and 4f metals in terms of exchange and anisotropy, and are therefore under consideration as potential building blocks for the next generation of single‐molecule magnets. In this Perspective, a review of the recent development in this field is given, and some discrepancies between the spectroscopic and magnetic data are discussed. © 2014 European Commission. International Journal of Quantum Chemistry published by Wiley Periodicals, Inc. 相似文献
99.
100.
Mitsumoto K Oshiro E Nishikawa H Shiga T Yamamura Y Saito K Oshio H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(35):9612-9618
Cyanide‐bridged metal complexes of [Fe8M6(μ‐CN)14(CN)10 (tp)8(HL)10(CH3CN)2][PF6]4?n CH3CN?m H2O (HL=3‐(2‐pyridyl)‐5‐[4‐(diphenylamino)phenyl]‐1H‐pyrazole), tp?=hydrotris(pyrazolylborate), 1 : M=Ni with n=11 and m=7, and 2 : M=Co with n=14 and m=5) were prepared. Complexes 1 and 2 are isomorphous, and crystallized in the monoclinic space group P21/n. They have tetradecanuclear cores composed of eight low‐spin (LS) FeIII and six high‐spin (HS) MII ions (M=Ni and Co), all of which are bridged by cyanide ions, to form a crown‐like core structure. Magnetic susceptibility measurements revealed that intramolecular ferro‐ and antiferromagnetic interactions are operative in 1 and in a fresh sample of 2 , respectively. Ac magnetic susceptibility measurements of 1 showed frequency‐dependent in‐ and out‐of‐phase signals, characteristic of single‐molecule magnetism (SMM), while desolvated samples of 2 showed thermal‐ and photoinduced intramolecular electron‐transfer‐coupled spin transition (ETCST) between the [(LS‐FeII)3(LS‐FeIII)5(HS‐CoII)3(LS‐CoIII)3] and the [(LS‐FeIII)8(HS‐CoII)6] states. 相似文献