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71.
72.
On the basis of pulse-energy measurement of Nd–YAG laser emission, the reflection coefficient of complex mirror is determined as a function of pumping energy and resonator parameters. It is shown that the reflection coefficient of complex mirror has the tendency to stabilize with increasing pumping energy above the threshold energy. The practical interest of this work is to determine the reflection coefficient of resonant mirror without using calibrated mirrors. 相似文献
73.
Baklouti L Cherif J Abidi R Arnaud-Neu F Harrowfield J Vicens J 《Organic & biomolecular chemistry》2004,2(19):2786-2792
A series of mixed [2 + 2'] p-tert-butylcalix[4]arene have been synthesised by selective 1,3-dialkylation of phenolic groups using various alkylating agents such as benzyl bromide, methyl iodide, ethyl bromoacetate, and 2-methoxyethyl tosylate. The extraction and complexation properties of the synthesized calixarenes towards alkali and alkaline earth metal cations have been investigated in acetonitrile by means of UV spectrophotometry and 1H NMR spectroscopy. The results show the formation of ML and/or ML2 species depending on the ligand and the cation. The enthalpies and entropies of complexation of alkali metal cations by a tetraglycol, diglycol-dibenzyl and diglycol-diester derivatives have been obtained from calorimetric measurements. The results revealed that the formation of ML species is controlled by enthalpy while the formation of ML2 from ML is entropy driven. 相似文献
74.
Abidi Jamel 《Rendiconti del Circolo Matematico di Palermo》2002,51(3):411-424
Résumé On établira dans ce papier le lien biunivoque entre fonctios plurisousharmoniques et fonctions holomorphes.
We prove in this paper the connection between plurisubharmonic and holomorphic functions.相似文献
75.
An efficient, direct allylic amination of both cyclic and acyclic Morita–Baylis–Hillman alcohols with aromatic amines, in tetrahydrofuran (THF) at room temperature, catalyzed by Pd(0)/Et3B, is reported herein. The corresponding amines are obtained with a high α -regioselectivity in 65–87% yields. 相似文献
76.
L. U. Joshi M. D. Zingde S. A. H. Abidi 《Journal of Radioanalytical and Nuclear Chemistry》1983,79(2):317-323
The surface leaching of the labile component of uranium has been carried out in estuarine sediments of Zuari river in Goa. The measurements of alpha activities of238U,235U and234U in the leachates indicated a remarkable anomaly between the activities of238U and234U. The activity ratios of234U/238U in these leachates have been found to be in the range of 1.10 to 1.14. However, the activity ratios of235U/238U have been found to be 0.045 which is close to that in natural uranium. It has also been observed that the anomaly between238U and234U exists only on the surface organic layers of the backwater sediments of the Zuari river. 相似文献
77.
Molecular species of neutral phospholipids, phosphatidylcholine (PC) and phosphatidylethanolamine (PE), were resolved by reversed-phase high-performance liquid chromatography (HPLC) using mobile phases of acetonitrile-methanol-water containing tetraalkylammonium phosphates (TAAPs). Competitive interactions of TAAPs and analyte solutes with a reversed-phase HPLC column resulted in reduced retention of PC or PE with concomitant increase in detection sensitivity. The chromatographic data for PC and PE were distinctly different from those for negatively charged phospholipids where ion-pair retention mechanisms prevailed. While PC (or PE) components eluted at longer retention times with a larger size of TAAP, an increase in the TAAP concentration invariably caused a decrease in phospholipid retention times. Optimization of HPLC conditions by using high concentrations (25-100 mM) of tetramethylammonium phosphate in acetonitrile-methanol-water (70:22:8) facilitated elution of components with improved peak symmetry. HPLC separations of neutral phospholipids derived from animal sources were more complex than those from soybeans. 相似文献
78.
Abidi R Baklouti L Harrowfield JM Sobolev AN Vicens J White AH 《Organic & biomolecular chemistry》2003,1(18):3144-3146
Determination of the crystal structure of the acetonitrile inclusate of the complex formed between sodium trifluoromethanesulfonate (triflate, CF3SO3-) and the narrow-rim functionalised calix[4]arene, 5,11,17,23-tetra-tert-butyl-25,27-di(phenylmethoxy)-26,28-di(2'-methoxyethoxy)calix[4]arene, has shown, somewhat unexpectedly, that the diether pendent arms do not chelate the sodium cation, although coordination of all four phenolic oxygen atoms does draw the calixarene into a nearly symmetrical cone form, consistent with conclusions drawn earlier from solution 1H NMR data. Crystals of C64H80O6.NaO3S.CF3.CH3CN obtained from acetonitrile solvent are monoclinic, C2/c, a structure determination at 'low' temperature (153 K) resolving several difficulties encountered in earlier attempts to analyse data acquired at approximately 295 K, and indicative of an interesting temperature dependence of substituent and anion orientations. 相似文献
79.
Abdelwaheb Hamdi Rym Abidi Zouhair Asfari Jacques Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》2003,45(1-2):97-105
The synthesis of four new tetraamido-type p-tert-butylcalix[4]arenes presenting two proximal binding subunits is reported. Complexation of alkalimetals and zinc picrates with these ligands have been carried out and monitored by 1H-NMR inCDCl3. It is shown that hard cations are included in the tetraamido cavity while thezinc cation is chelated to the pyridine rings of one of the ligands. The formation of a 1:1:1heterobinuclear complex is also described 相似文献
80.
Najah Cheriaa Rym Abidi Jacques Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》2008,60(3-4):303-312
Four imidazolyl acetamido p-tert-butylcalix[4]arenes 5–8 have been prepared by reacting the corresponding methyl esters derivatives 1–4 with histamine in 1:1 mixture of methanol:toluene. The yields ranged from 56 to 68%. 5–8 have been shown to be in cone conformation. The complexation behaviour of 5–8 towards monovalent metal picrates M+Pic− with M+ = Li+, Na+, K+, Rb+ and Cs+ and divalent metal picrates M2+(Pic−)2 with M2+ = Mg2+, Ca2+, Sr2+, Ba2+, Pb2+, Cd2+, Zn2+ and Co2+ are given. Tentative localisation of the metal cations in the receptors is given. The binding properties towards these cations
have been determined along with stoichiometries of the complexes. 相似文献