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21.
本文研究了俘获于掺杂VO++离子的(NH4)2Zn(SO4)2·6H2O单晶中NH3+自由基离子的ESR.从实验上分别测出π电子自由基NH3+的14N和15N核超精细分裂.结果表明,氮核超精细偶合张量具有近似于圆柱形对称。对于15N来说,A11=44.8,A22=19.3,A33=17.8高斯.对于14N来说,A11=31.1,A22=12.5,A33=11.8高斯.在室温下,NH3+自由基绕A11方向作圆锥体运动.文中最后讨论了NH3+自由基离子的可能生成机理。 相似文献
22.
Auslender, Cominetti and Haddou have studied, in the convex case, a new family of penalty/barrier functions. In this paper, we analyze the asymptotic behavior of augmented penalty algorithms using those penalty functions under the usual second order sufficient optimality conditions, and present order of convergence results (superlinear convergence with order of convergence 4/3). Those results are related to the analysis of pure penalty algorithms, as well as augmented penalty using a quadratic penalty function. Limited numerical examples are presented to appreciate the practical impact of this local asymptotic analysis.This research was partially supported by NSERC grant OGP0005491 相似文献
23.
We introduce the set of bicomplex numbers
which is a commutative ring with zero divisors defined by
where
We present the conjugates and the moduli associated with the bicomplex numbers. Then we study the bicomplex Schr?dinger equation
and found the continuity equations. The discrete symmetries of the system of equations describing the bicomplex Schr?dinger
equation are obtained. Finally, we study the bicomplex Born formulas under the discrete symmetries. We obtain the standard
Born’s formula for the class of bicomplex wave functions having a null hyperbolic angle. 相似文献
24.
25.
使用含时密度泛函理论(TDDFT)B3LYP方法计算了IB, IIB, VIIIB过渡金属与8-羟基喹啉络合(MQ)后, 配合物的电子光谱以及二阶非线性光学性质. 结果表明, 掺杂过渡金属后, 形成络合物的能隙值减小100~150 kJ/mol, 最大吸收波长红移150~200 nm左右. 电子从基态到激发态的跃迁主要为p→p*, n→p*跃迁, 属于LLCT, MLCT过程. IB的络合物MQ以及VIIIB的络合物MQ3表现出良好的非线性光学性质. 相似文献
26.
历代反动派总是宣扬孔老二“上智与下愚不移”的唯心论说教,把它作为“剥削有理”、“压迫有理”的根据。林彪这个地主资产阶级的代理人,为了篡党夺权,复辟资本主义,建立林家法西斯王朝,也鼓吹“上智下愚”的谬论。他把自己吹成“生而知之”的“天才”,以“至贵”、超人自居,污蔑劳动人民“愚昧”、“落后”,只会说“恭喜发财”,只能想“油盐酱醋柴”。 相似文献
27.
Thin-layer chromatographic screening procedure for undeclared synthetic drugs in Chinese herbal preparations 总被引:2,自引:0,他引:2
A simple and rapid thin-layer chromatographic procedure was developed for the detection and presumptive identification of seventeen synthetic drugs previously reported as adulterants of Chinese herbal preparations. Depending on its complexity, the sample may be directly extracted into aqueous ethanol, or stepwise fractionated into acidic, basic, and neutral components. Extracts are analyzed on silica gel layers containing a fluorescent indicator with the aid of two solvent systems. Spots are visualized under short and long wavelength ultraviolet lights. The procedure was successfully tested on synthetic and commercial samples. 相似文献
28.
Hoogesteger FJ van Walree CA Jenneskens LW Roest MR Verhoeven JW Schuddeboom W Piet JJ Warman JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(16):2948-2959
The photophysical properties of a bicyclohexylidene (1DA) and a bicyclohexyl (2DA) substituted with an anilino electron donor and a dicyanoethylene electron acceptor have been studied. Quenching of local donor emission is observed for these compounds as well as quenching of the "pseudo-local" acceptor emission. Transient absorption spectra show dialkylanilino-type radical-cation and dicyanoethylene-type radical-anion absorptions. These results show that intramolecular charge separation takes place in 1DA and 2DA. This was corroborated by time-resolved microwave conductivity measurements from which large excited-state dipole moments were found for both 1DA and 2DA. Time-resolved fluorescence spectroscopy revealed that in the charge-separated state in cyclohexane for 2DA, molecular folding takes place on a nanosecond timescale. For 1DA in cyclohexane, either charge separation takes place in a (fully) folded conformation or very rapid (subnanosecond timescale) folding takes place subsequent to charge separation. In addition to this difference in conformational behavior, the presence of the exocyclic double bond between the cyclohexyl-type rings results in efficient quenching of the anilino donor triplet state and acceleration of the charge recombination rate by a factor of 20. 相似文献
29.
30.
General reversed-phase high-performance liquid chromatographic method for the separation of drugs using triethylamine as a competing base 总被引:2,自引:0,他引:2
Triethylamine (TEA) was evaluated as a competing base for the retention control and peak shape improvement in the reversed-phase high-performance liquid chromatographic (RP-HPLC) analysis of selected acidic, basic, and neutral drugs. The effects of this amine on the capacity factor and theoretical plate number values of ephedrine, phenol, and sulfamerazine were examined on three unmodified commercial octadecylsilane chromatographic columns. Based on these results, a general RP-HPLC elution scheme using a mu Bondapak C18 10-micron column, methanol-acetic acid-TEA-water mobile phases, and an ultraviolet detector was developed for more than 150 drugs of pharmaceutical interest. The proposed method was applied to the separation of groups of chemically or pharmacologically related drugs that included sympathomimetic amines, antihistamines, phenothiazines, local anesthetics, Cinchona and tropane alkaloids, xanthines, sulfonamides, and steroids. In addition, paired-ion drugs such as physostigmine salicylate and combinations of ascorbic acid, benzoic acid, salicylic acid, pamoic acid, and 8-chlorotheophylline with various basic moieties were readily and effectively resolved into their ionic components using almost identical RP-HPLC conditions. 相似文献