全文获取类型
收费全文 | 41篇 |
免费 | 3篇 |
专业分类
化学 | 37篇 |
数学 | 1篇 |
物理学 | 6篇 |
出版年
2024年 | 1篇 |
2022年 | 1篇 |
2021年 | 1篇 |
2019年 | 2篇 |
2014年 | 6篇 |
2013年 | 1篇 |
2012年 | 1篇 |
2011年 | 2篇 |
2010年 | 1篇 |
2007年 | 2篇 |
2006年 | 1篇 |
2004年 | 1篇 |
2003年 | 1篇 |
2002年 | 3篇 |
1997年 | 1篇 |
1994年 | 1篇 |
1993年 | 1篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1971年 | 2篇 |
1970年 | 1篇 |
1965年 | 1篇 |
1958年 | 1篇 |
1936年 | 1篇 |
排序方式: 共有44条查询结果,搜索用时 15 毫秒
1.
Transition Metal Phosphido Complexes. VIII. X-Ray Diffraction Studies of Transition Metal Phosphorus Four- and Six-Membered Ring Complexes. Structures of [(CO)4MnPH2]2, [(CO)4MnPH2]3, and [cpNiPH2]3 [(CO)4MnPH2]2 1 crystallizes triclinic in the space group P1 with a = 680.4 pm, b = 706.4 pm, c = 919.1 pm, α 110.5°, β = 91.92°, γ 115.65°, and Z = 1 formula unit. The molecule exhibits a centrosymmetrical structure. The bond angles within the planar four-membered (Mn? P)2-ring are 76.1° at the Mn atoms and 103.9° at the P atoms, respectively. The average Mn? P bond distance is found to be 235.1 pm. [(CO)4MnPH2]3 2 crystallizes monoclinic in the space group P2/n with a = 905.2 pm, b = 974.8 pm, c = 1264.2 pm, β = 109.1°, and Z = 2 formula units. The framework of the six-membered (Mn? P)3-ring can be described as having a twist boat conformation. The average endocyclic bond angles are with 89.1° at the Mn atoms and 130.1° at the P atoms, respectively, largely widened compared to 1 . The average Mn? P bond distance, which is found to be 238.5 pm, is also slightly increased compared to 1 . [cpNiPH2]3 3 crystallizes rhombohedral in the space group R3. The cell constants (hexagonal setting) are a = b = 1686.1 pm, c = 561.1 pm and Z = 3 formula units. The six-membered (Ni? P)3-ring exhibits a chair conformation. The endocyclic bond angles are with 92.3° at the Ni atoms and 124.3° at the P atoms, respectively, comparable with those of the six-membered ring compound 2 . The Ni? P bond distance is found to be 215.2 pm. The eyclopentadienyl ligands are disordered and have been refined as rigid groups. 相似文献
2.
A sample pretreatment technique for silicon nitride involving digestion and matrix/traces separation was developed by means of radiotracers and applied to analysis of this material by inductively coupled plasma atomic emission spectrometry, inductively coupled plasma mass spectrometry and graphite furnace atomic absorption spectrometry. The results obtained for a high purity silicon nitride material by these methods are compared each with the other and with those obtained by neutron activation analysis. The limits of detection and the capabilities of the methods are compared and discussed. 相似文献
3.
Contributions to the Chemistry of Halosilane Adducts. XVI. Synthesis, Properties, Crystal and Molecular Structure of Hexa(N,N-dimethylformamide)silicon(IV)-tetraiodide When SiI4 is reacted with DMF ionization of all SiI bonds occurs to give ( 2 ) (reaction of pure components) or ( 1 ) (CHCl3 solution). IR and 1H-NMR spectra are in accordance with the formation of the octahedral cation [Si · 6 DMF]4+, DMF being coordinated through the CO group. 1 is only slowly attacted by methanol or water DMF being liberated. 1 crystallizes in the monoclinic space group C2/c with 4 formula units per unit cell. The cation [Si · 6 DMF]4+ has 1 symmetry. DMF is coordinated to Si in trans-configuration with respect to NMe2 with donation by oxygen. SiO bond distances (175.4–177.2 pm) correspond to those of [Si(O2C6H4)3]2? and [Si(acac)3]+; an increase of the CO distances (126.1–128.9 pm) and decrease of the CN distances (126.4–129.1 pm) as compared to free DMF is observed. These changes and structural data are discussed. 相似文献
4.
Stefan Sutorius Dr. David van Gerven Dr. Selina Olthof Dr. Bertold Rasche Dr. Jörn Bruns 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(22):e202200004
(SO4)-rich silicate analogue borosulfates are able to stabilise cationic cluster-like and chain-like aggregates. Single crystals of [Au3Cl4][B(S2O7)2] and [Au2Cl4][B(S2O7)2](SO3) were obtained by solvothermal reaction with SO3, and the electronic properties were investigated by means of density functional theory–based calculations. [Au3Cl4][B(S2O7)2] exhibits a cluster-like cation, and the cationic gold-chloride strands in [Au2Cl4][B(S2O7)2](SO3) are found to resemble one-dimensional metallic wires. This is confirmed by polarisation microscopy. 相似文献
5.
Martin Heise Bertold Rasche Dr. Anna Isaeva Dr. Alexey I. Baranov Prof. Dr. Michael Ruck Konrad Schäfer Prof. Dr. Rainer Pöttgen Jens‐Peter Eufinger Prof. Dr. Jürgen Janek 《Angewandte Chemie (International ed. in English)》2014,53(28):7344-7348
Nanoparticles of Bi3Ir, obtained from a microwave‐assisted polyol process, activate molecular oxygen from air at room temperature and reversibly intercalate it as oxide ions. The closely related structures of Bi3Ir and Bi3IrOx (x≤2) were investigated by X‐ray diffraction, electron microscopy, and quantum‐chemical modeling. In the topochemically formed metallic suboxide, the intermetallic building units are fully preserved. Time‐ and temperature‐dependent monitoring of the oxygen uptake in an oxygen‐filled chamber shows that the activation energy for oxide diffusion (84 meV) is one order of magnitude smaller than that in any known material. Bi3IrOx is the first metallic oxide ion conductor and also the first that operates at room temperature. 相似文献
6.
Bertold Laschinger 《Archiv der Mathematik》1986,47(3):281-288
Ohne Zusammenfassung 相似文献
7.
The SuperNEMO experiment is being designed to search for neutrinoless double beta decay. Its experimental technique of tracking and calorimetry provides the means to discriminate different underlying mechanisms for neutrinoless double beta decay by measuring the angular and energy distributions of electrons. The results of a study by the SuperNEMO Collaboration and F. Deppisch (in preparation) [7] for identifying light Majorana neutrino exchange and right-handed currents are presented. 相似文献
8.
Bertold Rasche Minjun Yang Lothar Nikonow Joshaniel F. K. Cooper Claire A. Murray Sarah J. Day Karin Kleiner Simon J. Clarke Richard G. Compton 《Angewandte Chemie (International ed. in English)》2019,58(43):15401-15406
We report the precise postsynthetic control of the composition of β‐Fe1+xSe by electrochemistry with simultaneous tracking of the associated structural changes via in situ synchrotron X‐ray diffraction. We access the full phase width of 0.01<x<0.04 and identify the superconducting state below 8 K, which in contrast to earlier reports is independent of the composition. However, in a second set of in situ X‐ray diffraction experiments, we demonstrate that β‐Fe1+xSe forms a new phase in the presence of oxygen above a 100 °C which has the same anti‐PbO type structure but is not superconducting down to 1.8 K. The latter process can be reversed electrochemically to reinstate the superconducting state. These observations exploit the exquisite control afforded by electrochemistry in contrast with classical approaches of chemical synthesis. 相似文献
9.
Superconductivity is a riddling phenomenon. Even after more than a century of research, the mechanism that drives the so-called ‘unconventional’ superconductors has not been fully understood. Although the phenomenon is closely linked to low-temperature research which is usually not the preferred condition for an electrochemist, the structures itself determining the superconducting behaviour are synthesised, studied and modified at much higher temperatures. Electrochemistry provides an unmatched lever to change the thermodynamic ground state and to modify or synthesise compounds. Concomitantly, it affords a precision for the investigation of compositions superior to other chemical methods. In this review, the example of the iron-based superconductor β-Fe1+xSe is chosen to evaluate achievements and prospects of this research at the cross section of (electro)chemistry and (solid state) physics. 相似文献
10.