全文获取类型
收费全文 | 93篇 |
免费 | 2篇 |
专业分类
化学 | 30篇 |
晶体学 | 1篇 |
力学 | 2篇 |
数学 | 17篇 |
物理学 | 45篇 |
出版年
2018年 | 2篇 |
2017年 | 1篇 |
2016年 | 1篇 |
2015年 | 2篇 |
2014年 | 4篇 |
2013年 | 6篇 |
2012年 | 2篇 |
2011年 | 2篇 |
2010年 | 3篇 |
2009年 | 3篇 |
2008年 | 1篇 |
2007年 | 4篇 |
2005年 | 6篇 |
2004年 | 3篇 |
2003年 | 1篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 4篇 |
1999年 | 3篇 |
1997年 | 2篇 |
1996年 | 1篇 |
1995年 | 5篇 |
1994年 | 5篇 |
1993年 | 5篇 |
1992年 | 4篇 |
1991年 | 3篇 |
1990年 | 1篇 |
1988年 | 1篇 |
1986年 | 6篇 |
1985年 | 5篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 1篇 |
1936年 | 1篇 |
排序方式: 共有95条查询结果,搜索用时 15 毫秒
1.
A. Caubet A. Labarta R. Rodríguez A. Fernandez E. Molins V. Moreno J. Tejada 《Hyperfine Interactions》1986,28(1-4):773-776
By means of57Co Mössbauer emission spectroscopy and magnetic susceptibility measurements, the local symmetries and electronic structure of the Co(II) ions in the Co-5IMO and Co-5GMP complexes in the hydrated and dehydrated forms have been determined. 相似文献
2.
Elías Molins Amílcar Labarta Javier Tejada Amparo Caubet Santiago Alvarez 《Transition Metal Chemistry》1983,8(6):377-380
Summary Magnetic moments and57Fe Mössbauer spectra at room temperature and at liquid nitrogen temperature of polynuclear ligand-bridged iron phthalocyanines, FePcL (L = pyrazine and 4,4-bipyridyl), are reported. The experimental data are in agreement with a pseudo-octahedral environment around the iron(II) cation. Partially oxidized derivatives, FePc(pz)I0.26 and FePc(bipy)I1.06 have been synthesized and their57Fe Mössbauer spectra and magnetic moments within the same temperature range obtained. Oxidation is shown to be metal centred and the iodine is found to be in I– form for FePc(pz)0.26 and as both I– and I
3
–
species for FePc(bipy)I1.06. While the magnetic moment of FePc(pz) increases upon oxidation, the opposite occurs for FePc(bipy). 相似文献
3.
Philippe Gerbier Daniel Ruiz-Molina Neus Domingo David B. Amabilino José Vidal-Gancedo Javier Tejada David N. Hendrickson Jaume Veciana 《Monatshefte für Chemie / Chemical Monthly》2003,134(2):265-276
Summary. A new modified approach for the synthesis of Mn12 clusters, based on the use of complex [Mn12O12(O2C
t
Bu)16(H2O)4] (2) as starting material to promote the acidic ligand replacement, is presented here. This new synthetic approach allowed us
to obtain complex [Mn12O12(O2CC6H4N(O•)
t
Bu)16(H2O)4] (3), whose preparation remained elusive by direct replacement of the acetate groups of Mn12Ac (1). Complex 3 bearing open-shell radical units, was prepared to increase the total spin number of its ground state, and consequently, to
increase T
B
, with the expectation that the radical ligands may couple ferromagnetically with the Mn12 core. Unfortunately, magnetic measurements of complex 3 revealed that the sixteen radical carboxylate ligands interact antiferromagnetically with the Mn12 core to yield a S = 2 magnetic ground state.
Corresponding author. E-mail: vecianaj@icmab.es
Received March 27, 2002; accepted May 2, 2002 相似文献
4.
5.
6.
F. FRÉZARD A. GARNIER-SUILLEROT C. DEMICHELI 《Journal of inclusion phenomena and macrocyclic chemistry》1997,28(1):51-62
The recent discovery that mithramycin(MTR) in aqueous solution forms a high affinity[Ca(MTR)4]2- complex led us to the idea thatCa2+-loaded liposomes might be able to accumulateMTR in their aqueous internal compartment. Wetherefore investigated the uptake of MTR into largeunilamellar vesicles (LUV) containing NaCl orCaCl2. Our data show that MTR was efficientlyaccumulated within LUV made fromdipalmitoylphosphatidylcholine and cholesterol, onlywhen the liposomes contained Ca2+ and wereresuspended in a Ca2+-free medium. A drugencapsulation efficiency as high as 60% was achieved,at a drug to lipid molar ratio of 1/18. The circulardichroism and fluorescence excitation spectra ofliposome-encapsulated MTR (LMTR) displayed strongsimilarities with those of the [Ca(MTR)4]2-complex. LMTR was found to be stable, when submittedto conditions that destabilized the[Ca(MTR)4]2- complex. Upon dilution andincubation for 24 h at 37 °C, MTR-containingliposomes did not release a significant amount of MTR.These properties were attributed to the formation ofa high affinity complex between MTR and Ca2+inthe aqueous compartment of liposomes. 相似文献
7.
8.
9.
10.
In this paper, we define a new rule for the resolution of the slack allocation problem in a PERT network. This problem exists of allocating existing extra time in some paths among the activities belonging to those paths. The allocation rule that we propose assigns extra time to the activities proportionally to their durations in such a way that no path duration exceeds the completion time of the whole project. This time allocation enables us to make a schedule for the PERT project under study. We give two characterizations of the rule and we compare it with others that have been previously defined in the literature. 相似文献