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1.
A.A Bessonov A.M FedosseevJ.-C Krupa I.B ShirokovaN.A Budantseva 《Journal of solid state chemistry》2002,169(2):182-188
A new method of synthesis of oxide tungsten bronzes containing lanthanide (Ln) Nd and Eu, based on thermal degradation of polyoxotungstate compounds, is proposed. The simplicity of the method allows to consider this class of compounds with chemical formula, LnxWO3, as potential inert target for incineration or transmutation of minor actinides, Am and Cm, in neutron reactors. Nd and Eu were used as analogues of transplutonium elements. Powder X-ray diffraction patterns of compounds synthesized reveal a cubic perovskite structure. The lanthanide content in bronzes was determined by optical spectroscopy analysis. The experimental density of the pressed bronze samples was estimated at 6.58 g cm−3, i.e., 89% of the crystallographic value. The thermal stability of the bronzes synthesized was checked up to 900°C in an inert atmosphere. Leaching tests were performed for europium bronzes in nitric acid solutions using luminescence technique. 相似文献
2.
Two new divalent samarocenes, Cp*′2Sm(THF) (1) and (CpPh3)2Sm(THF) (2) (Cp*′=C5Me4nPr, CpPh3=H2C5Ph3-1,2,4), were synthesized and characterized by 1H NMR and elemental analysis. The activity of 1 and 2 as butadiene polymerisation catalysts was studied, in the presence of MAO and MMAO, and compared to this of Cp*2Sm(THF)2 (3) and (Cp4i)2Sm (4) (Cp*=C5Me5, Cp4i=C5HiPr4), in the same conditions. The 1/MAO system presents the highest activity. The less active 2/MAO system leads to a high cis-1,4 regular structure up to 97%. The MMAO cocatalyst is found very sensitive to the steric hindrance of the samarocenes: the activity decreases from 1/MAO to 1/MMAO, and no activity is observed in the case of complexes 2 and 4, associated to MMAO. Complexes 1 and 2 can be both oxidized with AlMe3 to give the corresponding Sm/Al bimetallics and , respectively. 相似文献
3.
Enrique J. Baran 《Monatshefte für Chemie / Chemical Monthly》1979,110(2):297-300
Mean amplitudes of vibration for various octahedral complex compounds of the typeLnCl6
3– andLnBr6
3– (withLn=Nd, Eu, Gd, Dy, Er, and Yb) have been calculated, at different temperatures, using known spectroscopic data. The results are briefly discussed and it is found that theLn–Cl andLn–Br amplitude values are highly characteristic. 相似文献
4.
CoSm(SeO3)2Cl, CuGd(SeO3)2Cl, MnSm(SeO3)2Cl, CuGd2(SeO3)4 and CuSm2(SeO3)4: Transition Metal containing Selenites of Samarium and Gadolinum The reaction of CoCl2, Sm2O3, and SeO2 in evacuated silica ampoules lead to blue single crystals of CoSm(SeO3)2Cl (triclinic, , Z = 4, a = 712.3(1), b = 889.5(2), c = 1216.2(2) pm, α = 72.25(1)°, β = 71.27(1)°, γ = 72.08(1)°, Rall = 0.0586). If MnCl2 is used in the reaction light pink single crystals of MnSm(SeO3)2Cl (triclinic, , Z = 2, a = 700.8(2), b = 724.1(2), c = 803.4(2) pm, α = 86.90(3)°, β = 71.57(3)°, γ = 64.33(3)°, Rall = 0.0875) are obtained. Green single crystals of CuGd2(SeO3)2Cl (triclinic, , Z = 4, a = 704.3(4), b = 909.6(4), c = 1201.0(7) pm, α = 70.84(4)°, β = 73.01(4)°, γ = 70.69(4)°, Rall = 0.0450) form analogously in the reaction of CuCl2 and Gd2O3 with SeO2. CoSm(SeO3)2Cl contains [CoO4Cl2] octahedra, which are connected via one edge and one vertex to infinite chains. The Mn2+ ions in MnSm(SeO3)2Cl are also octahedrally coordinated by four oxygen and two chlorine ligands. The linkage of the polyhedra to chains occurs exclusively via edges. Both, the cobalt and the manganese compound show the Sm3+ ions in eight and ninefold coordination of oxygen atoms and chloride ions. In CuGd(SeO3)2Cl the Cu2+ ions are coordinated by three oxygen atoms and one Cl— ion in a distorted square planar manner. One further Cl— and one further oxygen ligand complete the [CuO3Cl] units yielding significantly elongated octahedra. The latter are again connected to chains via two common edges. For the Gd3+ ions coordination numbers of ?8 + 1”? and nine were found. Single crystals of the deep blue selenites CuM2(SeO3)4 (M = Sm/Gd, monoclinic, P21/c, a = 1050.4(3)/1051.0(2), b = 696.6(2)/693.5(1), c = 822.5(2)/818.5(2) pm, β = 110.48(2)°/110.53(2)°, Rall = 0.0341/0.0531) can be obtained from reactions of the oxides Sm2O3 and Gd2O3, respectively, with CuO and SeO2. The crystal structure contains square planar [CuO4] groups and irregular [MO9] polyhedra. 相似文献
5.
The determination of lanthanides by Inductively Coupled Plasma Mass Spectrometry (ICP‐MS) is complicated by several spectral overlaps from M+, MO+ or MOH+ ions formed in the ICP. Especially, it is essential to avoid the spectral interferences from lighter lanthanide and Ba polyatomic ions on middle or heavier lanthanides. To tackle this problem, we have developed a mathematical correction method, which reduces all the spectral overlaps from oxide species of Pr, Nd, Ce and Sm over Gd, Tb, Dy and Ho, and Gd, Tb over Yb and Lu. It can also successfully correct the oxide and hydroxide interference of Ba over Eu. The effectiveness of the proposed the mathematical correction scheme is demonstrated for the USGS Standard Rock samples AGV‐1 and G‐2. The results show that the experimental data obtained by applying the mathematical correction scheme for lanthanides is in good agreement with the reported values, using pneumatic and ultrasonic nebulisation methods, for their ICP‐MS analysis. 相似文献
6.
Romain Heck 《Tetrahedron letters》2004,45(2):281-284
A new tripodal α-cyclodextrin having three ureido-bipyridyl tethers symmetrically distributed on its upper rim was prepared in one step by the polymer supported ‘phosphine imide’ reaction in a medium yield. As expected, the highly selective complexation properties towards ‘hard’ and ‘soft’ cations were maintained with regards to the URFT-Cd (upper rim fully tethered) family previously investigated. Its EuIII and TbIII lanthanide complex fluorescence behaviour clearly indicates that a limited number of tethers allow a better bis-heterocyclic antenna self-organisation around the cation leading to enhanced fluorescence properties. 相似文献
7.
The retention behavior of uranium, thorium and lanthanides has been investigated with amide modified reversed phase C18 supports using α-hydroxy isobutyric acid (α-HIBA) as the mobile phase. Four structurally different amide moieties namely, 4-hydroxy-N,N-dihexyl butyramide (4HHBA), 4-hydroxy-N,N-di-2-ethylhexylhexanamide (4HEHHA), bis(N,N,N′,N′-2-ethylhexyl)malonamide (B2EHM) and N-methyl-tris(dihexylcarbamoyl-3-methoxy)pivolamide (MTDCMPA) have been synthesized and studied. Among the various amide coated columns, the supports modified with 4HHBA, B2EHM and MTDCMPA exhibit an interesting retention for uranium and thorium, which is different from 4HEHHA modified support. The retention time for uranium and thorium increases with increasing amide concentration for 4HHBA, B2EHM and MTDCMPA supports, while the same decreases with increasing 4HEHHA content. However, the separation factor for uranium and thorium is greater on a 4HEHHA support, compared to an unmodified C18 column, reflecting the amide's preferential complexation of uranium over thorium.Columns modified with 4HHBA, B2EHM and MTDCMPA exhibit relatively higher retentions for lanthanides. However, MTDCMPA modified support shows a different elution profile for lanthanides compared to 4HHBA, and B2EHM modified columns. Individual separations of heavier lanthanides, i.e., from gadolinium to lutetium also have been achieved using 4HHBA and B2EHM modified supports.The influence of modifier content, mobile phase concentration and its pH on the retention of metal ions has also been studied. Based on these investigations, an efficient high performance liquid chromatographic method (HPLC) has been developed for the rapid separation of uranium from thorium as well as for the individual separation of heavier lanthanides. 相似文献
8.
Joachim Angelkort Sander van Smaalen Prof. Dr. Sven Oliver Hauber Mark Niemeyer 《无机化学与普通化学杂志》2007,633(7):1031-1035
Single crystal X‐ray diffraction of Eu(SC36H49)2 has revealed a first order phase transition at a temperature of 119 K, that involves a reduction of the specific volume by 1 %. The transition corresponds to a doubling of the unit cell, as it is the result from reorientations of isopropyl groups that appear at peripheral sites of the organic ligands. It is argued that a denser packing is achieved at the expense of a less favourable conformation of one of the two crystallographically‐independent complexes in the low‐temperature phase. The Bond‐Valence method is used to show that interactions of equal strengths are present between europium and both sulphur atoms and both coordinating phenyl rings. 相似文献
9.
Ingo Hartenbach Falk Lissner Tanja Nikelski Steffen F. Meier Helge Müller‐Bunz Thomas Schleid 《无机化学与普通化学杂志》2005,631(12):2377-2382
About Lanthanide Oxotantalates with the Formula MTaO4 (M = La – Nd, Sm – Lu) Besides being a by‐product of solid state syntheses in tantalum ampoules the lanthanide(III) oxotantalates of the formula MTaO4 can be easily prepared by sintering lanthanide sesquioxide M2O3 and tantalum(V) oxide Ta2O5 with sodium chloride as flux. Under these conditions two structure types emerge depending upon the M3+ cationic radius. For M = La – Pr the MTaO4‐type tantalates crystallize in the space group P21/c with lattice constants of a = 762(±1), b = 553(±4), c = 777(±4) pm, β = 101(±1)° and four formula units per unit cell. With M = Nd, Sm – Lu, the monoclinic cell dimensions (space group P2/c) shrink to the lattice constants like a = 516(±9), b = 551(±9), c = 534(±9) pm, β = 96.5(±0.3)° and there are only two formula units present. Both structures show a coordination sphere of eight oxygen atoms for the lanthanide trications shaped as distorted square antiprism for the structure with the larger lanthanides (in the following referred to as A‐type) and as trigonal dodecahedron for the structure with the smaller ones (called as B‐type in the following). The coordination environment about the Ta5+ cations can be described as a slightly distorted octahedron (CN = 6) for the A‐type structure of MTaO4 and a heavily distorted one (CN = 6) for the B‐type. The difference between the two types results from the interconnection of these [TaO6]7? octahedra. Whereas they are connected via four vertices to form corrugated layers according to parallel the bc‐plane in the A‐type, the octahedra of the B‐type MTaO4 structure share edges to built up zig‐zag chains along the c axis. 相似文献
10.
镧系元素钨硼杂多酸盐的合成及性质研究 总被引:3,自引:0,他引:3
钨硼杂多配合是一类性能良好的催化剂,它还具有抗病毒作用,也可用于乳糖酶分离、纤维素光解剂及用于制造耐热油漆等,本文报道了K_(15)[Ln(BW_(11)O_(39))_2]·xH_2O(简称 相似文献