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The polymerisation reactions leading to the formation of polyphosphates of the composition (M′xM″1?x/2PO3)n where M′ = K, or Cs and M″ = Zn, Mg or Ni have been studied by thermogravimetric methods. Differential thermal analysis has been employed for the above reaction mixtures in case of potassium derivatives. TG and DTA curves confirm the formation of complex alkali polymetaphosphates of the composition as mentioned. The absence of lower phosphates and of other cyclic phosphates has been further confirmed by paper chromatographic studies of the above-mentioned complex derivatives as well as of many other alkali polymetaphosphates prepared in an analogous manner. 相似文献
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A series of mixed ligand cadmium(II) complexes having 3,5-dimethylpyrazole and aromatic carboxylate are structurally characterized. The effect of substituent on aromatic ring and also the effect of composition on co-ordination behavior of these complexes are ascertained. Hydrogen bonded self-assembled mononuclear complexes are obtained from composition [Cd(L)2(La)2] where La = 3,5-dimethylpyrazole L = R–C6H4COO– [R = H (1), 2-Cl (2), 4-OH (3), 2-OH (4)]. The cadmium complex (5) having composition [Cd(L)2(La)(H2O)] (L = 2-NO2–C6H4COO–) is tetra-nuclear. The complex has eight and six co-ordination around cadmium and self-assembles through hydrogen bonding leading to form extended chain structure. The four complexes (1–4) have six co-ordinated trigonal prismatic geometry around cadmium ions. Cadmium complexes having composition [Cd(L)2(La)] such as R = 4-NO2 (6), 4-Cl (7), and 1-naphthoate complex (8) are co-ordination polymers with seven co-ordination geometry around cadmium. In these co-ordination polymers different Cd–Cd distances are observed for alternate pair of cadmium ions. For example in the case of the co-ordination polymer of 4-nitro-benzoate complex the Cd–Cd distance between alternate pairs are 4.138 Å, and 3.748 Å. The 1-naphthoate complex having pyridine has composition [Cd(L)2(Lb)2](H2O)] (9) where Lb = pyridine and L = 1-naphthoate has seven co-ordination with a distorted pentagonal bipyramid geometry. 相似文献
25.
Y Wang L Davidow AC Arvanites J Blanchard K Lam K Xu V Oza JW Yoo JM Ng T Curran LL Rubin AP McMahon 《Chemistry & biology》2012,19(8):972-982
Highlights? Screened compound libraries for modulation of Smo movement to the primary cilium ? Identified glucocorticoids inducing Smo ciliary accumulation without activation ? They sensitize cells to Hh input and potentially modify the efficacy of Smo antagonists ? Identified a glucocorticoid inhibitor effective in inhibiting drug-resistant Smo mutants 相似文献
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Kusum Bania Nilotpal Barooah Rupam Sarma Jubaraj Bikash Baruah 《Journal of chemical crystallography》2008,38(1):57-60
Abstract The crystal structure of a metallohybrid carboxylic acid obtained from the reaction of 1,3,5-benzenetricarboxylic acid (TCAH3)
with copper(II)acetate monohydrate in the presence of pyridine (py) having composition Cu(py)2(TCAH2)2(H2O)2 [1] is reported. It crystallizes in triclinic space group P-1 and with a = 7.0110(3)?, b = 8.9523(5)?, c = 11.5370(5) ?,
α = 79.776(3) °, β = 82.881(3)°, γ = 83.628(3)°, and V = 704.18(6)?3. The hydrogen bond in 1 is compared with the hydrogen bond pattern in the structure of 1,3-dicarbomethoxy 4,6-benzenedicarboxylic
acid, which crystallizes in mononclinic space group P21/c and has unit cell parameters of a = 6.9549(16)?, b = 8.7676(15)?,
c = 20.111(4)?; β = 92.585(17) ° and V = 1225.1(4) ?3.
Index Abstract Crystal structure of a metallohybrid carboxylic acid obtained from the reaction of 1,3,5-benzenetricarboxylic acid with copper(II)acetate
monohydrate in the presence of pyridine is determined and compared with hydrogen bond pattern present in the structure of
1,3-dicarbomethoxy 4,6-benzenedicarboxylic acid.
Crystal structure of a metallohybrid acid of 1,3,5-benzenetricarboxylic acid of copper(II).
Kusum Bania, Nilotpal Barooah, Rupam Sarma, Jubaraj B. Baruah 相似文献
28.
Suresh K. Chamarthi Brian Raterman Ria Mazumder Anthony Michaels Veeral M. Oza James Hanje Bradley Bolster Ning Jin Richard D. White Arunark Kolipaka 《Magnetic resonance imaging》2014
Magnetic resonance elastography (MRE) of the liver is a novel noninvasive clinical diagnostic tool to stage fibrosis based on measured stiffness. The purpose of this study is to design, evaluate and validate a rapid MRE acquisition technique for noninvasively quantitating liver stiffness which reduces by half the scan time, thereby decreasing image registration errors between four MRE phase offsets. In vivo liver MRE was performed on 16 healthy volunteers and 14 patients with biopsy-proven liver fibrosis using the standard clinical gradient recalled echo (GRE) MRE sequence (MREs) and a developed rapid GRE MRE sequence (MREr) to obtain the mean stiffness in an axial slice. The mean stiffness values obtained from the entire group using MREs and MREr were 2.72 ± 0.85 kPa and 2.7 ± 0.85 kPa, respectively, representing an insignificant difference. A linear correlation of R2 = 0.99 was determined between stiffness values obtained using MREs and MREr. Therefore, we can conclude that MREr can replace MREs, which reduces the scan time to half of that of the current standard acquisition (MREs), which will facilitate MRE imaging in patients with inability to hold their breath for long periods. 相似文献
29.
Weak transitions of decuplet isobars are expanded in terms of eigen-amplitudes of the direct channel in the framework of SU(3).
Starting with the most general weak Hamiltonian and assuming intermediate states to be non-exotic, we obtain ΔI=1/2 rule for Ω− decays. Invoking of the CP invariance forbids all thepv weak processesD(10)→D(10) +P(8). Decays of the charmed multiplets are also discussed in these dynamical considerations. We obtain triplet dominance of
charm changing weak Hamiltonian for Ω*++
3 decays. 相似文献
30.
Total synthesis of (+)-boronolide, (+)-deacetylboronolide, and (+)-dideacetylboronolide has been achieved from a single intermediate 26, which was synthesized in 11 steps from a d-mannitol-derived intermediate 8 in an overall yield of 10%. The key steps in the synthesis are inversion of a chiral center by taking an advantage of the inherent mechanism involved in the ring closing to an epoxide via intramolecular S(N)2 reaction and lactonization of a diol using Fetizons reagent. The strategy is amenable to preparation of analogues of (+)-boronolide in sufficient amount for further screening of biological activity. 相似文献