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Matthias Ernst Aswin Verhoeven Beat H. Meier 《Journal of magnetic resonance (San Diego, Calif. : 1997)》1998,130(2):176-185
We have investigated the carbon line shape of solid adamantane under high-speed magic-angle sample spinning (MAS) acquired without proton decoupling. The CH-group shows a spinning-speed-dependent line broadening while the CH2-group consists of a spinning-speed-independent sharp component and a spinning-speed-dependent broader part. These phenomena can be explained by self-decoupling of theJ-interaction due to proton spin diffusion. Such a self-decoupling process can be described by a magnetization exchange process between the multiplet lines. Changing the spin-diffusion rate constant by off-resonance irradiation of the protons allows us to observe the full range from slow exchange to coalescence to fast exchange of the carbon spectra. One of the multiplet components in the CH2-group corresponds to a group spin of the protons of zero and therefore does not couple to the other protons. This gives rise to the sharp central line. The magnetization exchange rate constant between the different multiplet lines can be determined from the spectra and is a measure for the spinning-speed-dependent proton spin-diffusion rate constant. Even at an MAS speed of 30 kHz, proton spin diffusion is still observable despite the relatively weak intermolecular proton dipolar-coupling network in adamantane which results in a static proton line width of only 14 kHz (full width at half height). 相似文献
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A diastereospecific,non-racemic synthesis of a novel β-hydroxy-δ-lactone HMG-CoA reductase inhibitor
M. Sletzinger T.R. Verhoeven R.P. Volante J.M. McNamara E.G. Corley T.M.H. Liu 《Tetrahedron letters》1985,26(25):2951-2954
The coupling of acyl anion equivalent with chiral synthon , derived from isoascorbic acid, and a highly stereospecific reduction of the resulting β-hydroxy ketone highlight an efficient synthesis of β-hydroxy-δ-lactone . 相似文献
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The photoelectron spectra of 1-aza-adamantane, 1-aza-adamant-4-one and 1-aza-adamant-4-methylene are described and compared with those of the corresponding adamantane analogues. In the 1-aza-adamantane derivatives a through-bond interaction between the nitrogen lone-pair and the 4-substituent is observed. This through-bond interaction is discussed in relation with the sigma-coupled transition observed in the electronic absorption spectrum of 1-aza-adamantane derivatives, and in relation with their relative basicity both in solution and in the gasphase. 相似文献
89.
Verhoeven A Williamson PT Zimmermann H Ernst M Meier BH 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2004,168(2):4514-326
It is demonstrated that internuclear distances can be evaluated from rotational-resonance (RR) experiments in uniformly (13)C-labelled compounds. The errors in the obtained distances are less than 10% without the need to know any parameters of the spin system except the isotropic chemical shifts of all spins. We describe the multi-spin system with a simple fictitious spin-1/2 model. The influence of the couplings to the passive spins (J and dipolar coupling) is described by an empirical constant offset from the rotational-resonance condition. Using simulated data for a three-spin system, we show that the two-spin model describes the rotational-resonance transfer curves well as long as none of the passive spins is close to a rotational-resonance condition with one of the active spins. The usability of the two-spin model is demonstrated experimentally using a sample of acetylcholine perchlorate with labelling schemes of various levels of complexity. Doubly-, triply-, and fully labelled compounds lead to strongly varying RR polarization-transfer curves but the evaluated distances using the two-spin model are identical within the expected error limits and coincide with the distance from the X-ray structure. Rotational-resonance distance measurements in fully labelled compounds allow, in particular, the measurement of weak couplings in the presence of strong couplings. 相似文献
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M. A. F. A. Boons M. L. P. M. Verhoeven L. A. Ae. Sluyterman H. M. Buck 《Applied biochemistry and biotechnology》1989,22(1):95-107
Polymyxin B was immobilized on the ion exchanger, Amberlite IRC-50. The modified support was used as an adsorbent for lipopolysaccharide ofE. coli from a phosphate buffer at pH = 7.0 and T = 20°C. The insertion of a spacer, 6-amino hexanoic acid, improved the adsorption capacity of the modified carrier significantly. Upon partial acetylation (25%) of primary amino groups of immobilized Polymyxin B, the adsorption capacity of the support was halved. From our results, it is concluded that the complex formation between lipopolysaccharide and immobilized Polymyxin B is based on both lipophilic, as well as electrostatic, interactions. Convenient procedures for the immobilization of the ligands and the characterization of the ion exchanger are described. 相似文献