全文获取类型
收费全文 | 122篇 |
免费 | 1篇 |
专业分类
化学 | 98篇 |
晶体学 | 1篇 |
力学 | 3篇 |
数学 | 6篇 |
物理学 | 15篇 |
出版年
2023年 | 1篇 |
2022年 | 3篇 |
2021年 | 4篇 |
2019年 | 5篇 |
2018年 | 4篇 |
2017年 | 1篇 |
2016年 | 4篇 |
2015年 | 4篇 |
2014年 | 3篇 |
2013年 | 7篇 |
2012年 | 7篇 |
2011年 | 5篇 |
2010年 | 3篇 |
2009年 | 7篇 |
2008年 | 12篇 |
2007年 | 11篇 |
2006年 | 6篇 |
2005年 | 6篇 |
2004年 | 6篇 |
2003年 | 4篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1992年 | 2篇 |
1990年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1982年 | 1篇 |
1981年 | 3篇 |
1980年 | 2篇 |
1978年 | 1篇 |
排序方式: 共有123条查询结果,搜索用时 15 毫秒
51.
This study examined the effect of an on-frequency precursor on growth-of-masking (GOM) functions measured using an off-frequency masker. The signal was a 6-ms, 4-kHz tone. A GOM function was measured using a 40-ms, 2.8-kHz tone (the off-frequency masker). GOM functions were then measured with an on-frequency, fixed level precursor presented before the off-frequency masker. The precursor was 50 or 60 dB SPL, and 160 ms in duration. For the 60-dB SPL precursor, a 40-ms duration was also used. Two-line functions were fit to the GOM data to estimate the basilar membrane input-output function. The precursors reduced the gain of the input-output function, and this decrease was graded with precursor level. Both precursor durations had the same effect on gain. Changes in masking following a precursor were larger than would be predicted by additivity of masking. The observed decrease in gain may be consistent with activation of the medial olivocochlear reflex by the precursor. 相似文献
52.
53.
Jeannie Kibitel Vidya Hejmadit† Lori Alas Adrienne O'Connor Betsy M. Sutherland Daniel Yarosh 《Photochemistry and photobiology》1998,67(5):541-546
Ultraviolet light induces the expression of tumor necrosis factor α (TNFα) in many mammalian cells. We have examined the signal for this induction in a human DNA repair-deficient cell line carrying a transgene composed of the murine TNF regulatory sequences fused to the chloramphenicol acetyltransferase (CAT) structural gene. When compared by fluence, UVC was a more efficient inducer of CAT than was UVB, but they were equivalent inducers when compared by the frequency of cyclobutyl pyrimidine dimers produced by each source. Further, treatment of UV-irradiated cells with the prokaryotic DNA repair enzyme T4 endonuclease V in-creased the level of repair of dimers and concomitantly reduced CAT gene expression. Membrane-bound TNFα expression was increased by UV and reduced by repair of dimers. Finally, in the TNFcat transgene system, DNA damage directly to the cell with the transgene was required as cocultivation of unirradiated TNFcat cells with UV-irradiated cells did not increase CAT activity. These results show that DNA damage is a signal for the induction of TNFa gene expression in mouse and human cells. 相似文献
54.
Sundararajan K Vidya V Sankaran K Viswanathan KS 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2000,(10):1855-1867
Trimethyl phosphate (TMP) and acetylene were codeposited in nitrogen and argon matrices and adducts of these species were identified using infrared spectroscopy. Formation of the adducts was evidenced by shifts in the vibrational frequencies of the modes involving the TMP and acetylene submolecules. The structures of these adducts, energies and the vibrational frequencies were computed at the HF/6-31G** level. Both the experimental and computational studies indicated that two types of TMP-acetylene complexes were formed; one in which the hydrogen in acetylene was bonded to the phosphoryl oxygen and another in which the bonding was at the alkoxy oxygen of the phosphate. In addition to the primary hydrogen bonded interaction at the phosphoryl oxygen, this complex, also appeared to be stablilized by a secondary and weaker interaction involving a methyl hydrogen in TMP and the pi cloud in acetylene--a case of a H...pi interaction. The computed vibrational frequencies in the adducts agreed well with the observed frequencies for the modes involving the TMP submolecule, while the agreement was relatively poor for the modes involving the acetylene submolecule. The stabilization energies of these adducts, corrected for both zero-point energies and basis set superposition errors, were approximately 3 kcal/mol for the phosphoryl complex and, approximately 1 kcal/mol for the alkoxy complex. 相似文献
55.
Kiziltepe T Yan A Dong M Jonnalagadda VS Dedon PC Engelward BP 《Chemistry & biology》2005,12(3):357-369
Inflammation is an important risk factor for cancer. During inflammation, macrophages secrete nitric oxide (NO*), which reacts with superoxide or oxygen to create ONOO- or N2O3, respectively. Although homologous recombination causes DNA sequence rearrangements that promote cancer, little was known about the ability of ONOO- and N2O3 to induce recombination in mammalian cells. Here, we show that ONOO- is a potent inducer of homologous recombination at an integrated direct repeat substrate, whereas N2O3 is relatively weakly recombinogenic. Furthermore, on a per lesion basis, ONOO(-)-induced oxidative base lesions and single-strand breaks are significantly more recombinogenic than N2O3-induced base deamination products, which did not induce detectable recombination between plasmids. Similar results were observed in mammalian cells from two different species. These results suggest that ONOO(-)-induced recombination may be an important mechanism underlying inflammation-induced cancer. 相似文献
56.
Summary Trivalent chromium, manganese, iron and cobalt salts react withm-phenylenediamine and acetylacetone to give complexes of the type [M(C16H18N2O2)X]: X = Cl, Br, NO3 or NCS for M = chromium(III) and iron(III); X = Cl, Br, OAc or NCS for manganese(III); and X = OH for cobalt(III). Conductance measurements show the complexes to be nonelectrolytes. Molecular weights determined cryoscopically, show the iron complexes to be dinuclear. Magnetic measurements above 85 K reveal the presence of slight antiferromagnetic interactions. The complexes are dimeric five-coordinate square-pyramidal withm-phenylenediamine residues acting as bridges. The electronic spectra are interpreted in terms of the Normalised Spherical Harmonic Hamiltonian Theory and the DT/DQ values which indicate that chromium complexes are slightly distorted, whereas those of manganese are severely distorted. 相似文献
57.
Spin, charge, and orbital orderings are influenced by electron/hole doping, cation radii, oxygen stoichiometry, temperature, magnetic field, and so on. In order to understand the role of electron/hole doping, we have studied variations in spin, charge, and orbital ordering in terms of d-band filling for YBaT 2O 5 (T = Mn, Fe, Co). The calculations were performed using density functional theory as implemented in the full-potential linearized augmented-plane-wave method. We have carried out calculations for nonmagnetic, ferromagnetic, and antiferromagnetic configurations. A ferrimagnetic ground state was established for YBaMn 2O 5, whereas YBaFe 2O 5 and YBaCo 2O 5 have antiferromagnetic ground states; all of these results are in agreement with experimental findings. The effects of spin-orbit coupling, the Hubbard U parameter, and orbital polarization on the magnetic properties were also analyzed. The electronic band characteristics were analyzed using total as well as site- and orbital-projected densities of states. Inclusion of spin-orbit coupling and Coulomb correlation effects in the calculations was found to be important in order to reproduce the experimentally established semiconducting behaviors of YBaFe 2O 5 and YBaCo 2O 5. In order to quantify the charges at each atomic site, we made use of the Bader "atom-in-molecule" concept and Born effective-charge (BEC) analyses. The structural optimizations and BEC tensor calculations were performed using the VASP-PAW method. The different types of charge and orbital orderings in these compounds were visualized using the energy-projected density matrices of the d electrons. Substantial differences in ordering patterns with respect to d-band filling emerged. Ordering of the d z (2) orbital of Mn in YBaMn 2O 5 gave rise to G-type ferrimagnetic spin ordering along the c direction and checkerboard-type charge ordering, whereas ordering of the d x (2) - y (2) orbital of Fe in YBaFe 2O 5 caused Wollan-Koehler G-type antiferromagnetic spin ordering along the b direction and stripe-type charge ordering. Similarly, a complex pattern of orbital ordering in YBaCo 2O 5 activated spin and charge orderings similar to those in YBaFe 2O 5. 相似文献
58.
In an attempt towards the total synthesis of Pseudoxylallemycin B, a homo dimeric, N-methylated macrocyclic tetrapeptidic natural product, synthesis of its epimer at position 3 (d-Tyr instead of l-Tyr) is described here. During the course of synthesis we came across a striking yet unusual observation of complete epimerization which led to the formation of 3-epi-Pseudoxylallemycin B. 相似文献
59.
Radical reactions have been a fascinating arena in organic chemistry for decades and the rapid progress in this field is the topic of this review. Generation of radicals through sustainable catalysis using photoredox catalysts and iron based catalysts have significantly expanded the scope of radical reactions for carbon–carbon and carbon-heteroatom bond formations in recent years. Selective transformations using silver salts and other single electron transfer oxidants have also played significant roles. Cascade reactions based on radical intermediates have even widened the potential of radical reactions for carbocyclic and heterocyclic constructions. The recent advances (2014–2017) in radical based methods for CC bond formations are discussed in this digest review. 相似文献
60.
Avuthu Vidya Sagar Reddy Mudumala Veeranarayana Reddy Yeon Tae Jeong 《Research on Chemical Intermediates》2016,42(6):5209-5218
An environmentally benign, ultrasound-promoted synthesis of biologically active benzoxanthene derivatives has been developed by silica-supported tungstic acid as an efficient catalyst under solvent-free conditions. The major advantages of the present protocol are operational simplicity, use of an inexpensive catalyst, bypassing the chromatographic purification, good yields, and short reaction times. The catalyst could be reused at least five consecutive cycles, without loss of its catalytic activity. 相似文献