全文获取类型
收费全文 | 86篇 |
免费 | 0篇 |
专业分类
化学 | 29篇 |
力学 | 1篇 |
物理学 | 56篇 |
出版年
2021年 | 1篇 |
2019年 | 1篇 |
2018年 | 1篇 |
2017年 | 1篇 |
2016年 | 3篇 |
2013年 | 1篇 |
2012年 | 1篇 |
2011年 | 3篇 |
2009年 | 1篇 |
2008年 | 4篇 |
2007年 | 1篇 |
2006年 | 1篇 |
2005年 | 3篇 |
2002年 | 4篇 |
2001年 | 1篇 |
2000年 | 9篇 |
1999年 | 1篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 3篇 |
1995年 | 1篇 |
1994年 | 6篇 |
1992年 | 5篇 |
1990年 | 4篇 |
1989年 | 5篇 |
1988年 | 3篇 |
1987年 | 1篇 |
1986年 | 6篇 |
1985年 | 1篇 |
1983年 | 1篇 |
1982年 | 2篇 |
1977年 | 4篇 |
1976年 | 2篇 |
1975年 | 1篇 |
1974年 | 1篇 |
排序方式: 共有86条查询结果,搜索用时 15 毫秒
1.
2.
William J.?KraemerEmail author Jeff S.?Volek Barry A.?Spiering Jakob L.?Vingren 《Monatshefte für Chemie / Chemical Monthly》2005,136(8):1383-1390
Summary. Early research investigating the effects of L-carnitine supplementation has examined its role in substrate metabolism and in acute exercise performance. These studies have yielded equivocal findings, partially due to difficulties in increasing muscle carnitine concentrations. However, recent studies have proposed that L-carnitine may play a different role in exercise physiology, and preliminary results have been encouraging. Current investigations have theorized that L-carnitine supplementation facilitates exercise recovery. Proposed mechanism is as follows: 1) increased serum carnitine concentration enhances capillary endothelial function; 2) increased blood flow and reduced hypoxia mitigate the cascade of ensuing, destructive chemical events following exercise; 3) thus allowing reduced structural damage of skeletal muscle mediated by more intact receptors in muscle needed for improved protein signaling. This paradigm explains decreased markers of purine catabolism, free radical formation, and muscle tissue disruption after resistance exercise and the increased repair of muscle proteins following long-term L-carnitine supplementation. 相似文献
3.
Gaspar Ana B. Ksenofontov Vadim Spiering Hartmut Reiman Sergey Real José A. Gütlich Philipp 《Hyperfine Interactions》2002,144(1-4):297-306
This article reports on the study of the interplay between magnetic coupling and spin transition in 2,2′-bipyrimidine (bpym)-bridged
iron(II) dinuclear compounds. Coexistence of both phenomena has been observed in [Fe(bpym)(NCS)2]2bpym, [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym (bpym = 2,2′-bipyrimidine, bt = 2,2′-bithiazoline) by the action of external physical factors namely pressure or electromagnetic
radiation. Competition between magnetic exchange and spin crossover has been studied in [Fe(bpym)(NCS)2]2bpym at 6.3 kbar. LIESST experiments carried out in [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym at 4.2 K have shown that is possible to achieve dinuclear molecules with different spin states in this class of compounds.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
4.
H. Spiering V. Ksenofontov O. Leupold J. Kusz L. Deák Z. Németh C. Bogdán L. Bottyán D. L. Nagy 《Hyperfine Interactions》2016,237(1):58
The effect of selfabsorption in Mössbauer sources is studied in detail. Spectra were measured using an old 57 C o/R h source of 74M B q activity with an original activity of ca. 3.7G B q and a 0.15G B q 57 C o/α ? F e source magnetized by an in-plane magnetic field of 0.2 T. The 57 C o/α ? F e source of a thickness of 25 μ was used both from the active and the inactive side giving cause to very different selfabsorption effects. The absorber was a single crystal of ferrous ammonium sulphate hexahydrate (FAS). Its absorption properties were taken over from a detailed study (Bull et al., Hyperfine Interact. 94(1–3), 1; Spiering et al. 2). FAS (space group P21/c) crystallizes as flat plates containing the (\(\overline {2}\)01) plane. The γ-direction was orthogonal to the crystal plate. The 57 C o atoms of the 57 C o/R h source were assumed to be homogeneously distributed over a 6μ thick Rh foil and to follow a one dimensional diffusion profile in the 25 μ Fe-foil. The diffusion length was fitted to 10 μ. The theory follows the Blume-Kistner equations for forward scattering (Blume and Kistner, Phys. Rev. 171, 417, 3) by integrating over the source sampled up to 128 layers. 相似文献
5.
6.
Deák L. Bottyán L. Major M. Nagy D. L. Spiering H. Szilágyi E. Tanczikó F. 《Hyperfine Interactions》2002,144(1-4):45-52
Hyperfine Interactions - Synchrotron Mössbauer Reflectometry (SMR), the grazing incidence nuclear resonant scattering of synchrotron radiation, can be applied to perform depth-selective phase... 相似文献
7.
Using our new spectrometer for time-differential Mössbauer emission spectroscopy we reinvestigated the high-spin→low-spin relaxation following the57Co(EC)57Fe process in [57Co/Co(phen)3](ClO4)2 (phen=1,10-phenanthroline). In contrast to former investigations we found a temperature dependent initial population less than 1 for the metastable high-spin states. The results and the data evaluation method are presented. 相似文献
8.
9.
H. Spiering 《Hyperfine Interactions》1985,26(1-4):737-768
The angular dependence of the intensities of pure or mixed multipole transitions is formulated in a new fashion, which takes
into account arbitrary texture of the M?ssbauer absorber ranging from complete orientation (single crystals) over preferred
orientation to random powders and an anisotropic absorption fraction of the nuclei. The application of the theory is demonstrated
by means of typical examples from the literature. 相似文献
10.
Maartje M. C. Bastings Thomas M. Hermans A. J. H. Spiering Erwin W. L. Kemps Lorenzo Albertazzi Eva E. Kurisinkal Patricia Y. W. Dankers 《Macromolecular bioscience》2019,19(1)
The most basic function of synthetic microenvironments for tissue engineering is to act as a physical substrate for cell attachment, migration, and proliferation, similar to the natural cell environment. Functionalization of supramolecular materials with guest compounds that display the same recognition moieties is a common strategy to introduce biofunctionality. However, besides a robust interaction with the material, a certain level of dynamics needs to be conserved for an adaptive interface toward the living environment. A balance between robust material functionalization and dynamic cell interaction needs to be met. The detailed analysis hereof using a ureido‐pyrimidinone (UPy) poly(ethylene glycol) system in dilute and transient network regime is demonstrated. Monovalent and bivalent UPy‐functionalized guest molecules are designed and their interaction with UPy‐host fibers is evaluated. Analysis of guest interaction in the dilute state by microfluidics, and in the gel state, by fluorescence recovery after photobleaching and fluorescence resonance energy transfer is proven to be suitable to quantify the local and ensemble guest mobility. The results demonstrate that the interaction of bioactive moieties through supramolecular host–guest chemistry yields a dynamic system, which is stronger for divalent guests but risks unintended leakage in the case of functional monomeric units. 相似文献