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301.
Identification of isomeric N-glycan structures by mass spectrometry with 157 nm laser-induced photofragmentation 总被引:1,自引:1,他引:0
Devakumar A Mechref Y Kang P Novotny MV Reilly JP 《Journal of the American Society for Mass Spectrometry》2008,19(7):1027-1040
Characterization of structural isomers has become increasingly important and extremely challenging in glycobiology. This communication demonstrates the capability of ion-trap mass spectrometry in conjunction with 157 nm photofragmentation to identify different structural isomers of permethylated N-glycans derived from ovalbumin without chromatographic separation. The results are compared with collision-induced dissociation (CID) experiments. Photodissociation generates extensive cross-ring fragment ions as well as diagnostic glycosidic product ions that are not usually observed in CID MS/MS experiments. The detection of these product ions aids in characterizing indigenous glycan isomers. The ion trap facilitates MS(n) experiments on the diagnostic glycosidic fragments and cross-ring product ions generated through photofragmentation, thus allowing unambiguous assignment of all of the isomeric structures associated with the model glycoprotein used in this study. Photofragmentation is demonstrated to be a powerful technique for the structural characterization of glycans. 相似文献
302.
303.
P. Schläpfer E. Hofmann M. Nicloux I. G. Mc Chesney F. E. Vandaveer R. C. Gregg H. Schulze-Manitius H. Friedrich G. Neumann A. Schneider V. N. Morris N. P. Péntcheff H. Diergarten W. Liesegang L. C. Mc Nair J. F. Hirst R. C. Wiley A. Magnus H. Kratz W. H. Fulweiler Raßfeld J. T. Donnelly C. H. Foott J. Reilly J. A. Fries W. V. Hanks und W. H. Mc Adams 《Fresenius' Journal of Analytical Chemistry》1930,82(1-3):76-86
Ohne Zusammenfassung 相似文献
304.
L. W. Winkler E. Ekman A. Samyschlayewa W. Zimmermann K. Bodendorf N. Prileshajew L. Kofler F. Krämer P. HOrkheimer J. Reilly N. Noonan P. J. Drumm W. Peyer H. Iffinger S. Kroll W. J. Blackie J. F. Clevenger M. L. Pabst A. R. Bliss jun R. W. Morrison und E. O. Prather jun 《Fresenius' Journal of Analytical Chemistry》1935,102(3-4):141-146
Ohne Zusammenfassung 相似文献
305.
The aim of this paper is to introduce two kinds of generalized continuity for multifunctions. Basic properties and characterizations
of such multifunctions are established. These two generalized continuities include many of the variations of multifunction
continuity already in the literature as special cases.
相似文献
306.
He Y Parthasarathi R Raghavachari K Reilly JP 《Journal of the American Society for Mass Spectrometry》2012,23(7):1182-1190
Tris(2,4,6-trimethoxyphenyl) phosphonium acetyl (TMPP-Ac) was previously introduced to improve the mass spectrometric sequence analysis of peptides by fixing a permanent charge at the N-termini. However, peptides containing arginine residues did not fragment efficiently after TMPP-Ac modification. In this work, we combine charge derivatization with photodissociation. The fragmentation of TMPP-derivatized peptides is greatly improved and a series of N-terminal fragments is generated with complete sequence information. Arginine has a special effect on the fragmentation of the TMPP tagged peptides when it is the N-terminal peptide residue. Theoretical and experimental results suggest that this is due to hydrogen transfer from the charged N-terminus to the hydrogen-deficient peptide sequence. 相似文献
307.
Boland KS Conradson SD Costello AL Gaunt AJ Kozimor SA May I Reilly SD Schnaars DD 《Dalton transactions (Cambridge, England : 2003)》2012,41(7):2003-2010
We report the interaction between B-type tri-lacunary heteropolyoxotungstate anions and actinyl(V) cations in aqueous solution, yielding a greater understanding of the stability of the O≡An≡O(1+) linear dioxo actinide moiety. Previously we reported that B-α-[BiW(9)O(33)](9-) and B-α-[SbW(9)O(33)](9-) will react with NpO(2)(1+) to yield [(Np(3)W(4)O(15))(H(2)O)(3)(MW(9)O(33))(3)](18-) (M = Bi, or Sb). Single crystal structural characterisation of salts of these complexes revealed a core in which three Np(V) atoms interact with a central W(VI) atom through bridging oxo groups. These bridging oxygen atoms come from one of the two axial oxygens in O≡Np≡O(1+) and represent a highly unusual interaction for a discrete molecular species. In this study visible/near infra-red spectroscopy indicates that [(Np(3)W(4)O(15))(H(2)O)(3)(BiW(9)O(33))(3)](18-) could be readily stabilized in solution at near neutral pH for several months, with (NH(4))(14)Na(4)[(Np(3)W(4)O(15))(H(2)O)(39)BiW(9)O(33))(3)]·62H(2)O crystallising from solution in high yield. At lower pH and [BiW(9)O(33)](9-) : NpO(2)(1+) ratios additional Np(V) species could be observed in solution. Stabilization of [(Np(3)W(4)O(15))(H(2)O)(3)(SbW(9)O(33))(3)](18-) in solution proved more challenging, with several distinctive Np(V) near infra-red transitions observed in solution. Slow complexation kinetics and reduction to Np(IV) was also observed. High [SbW(9)O(33)](9-) : NpO(2)(1+) molar ratios and careful control of solution pH was required to prepare solutions in which [(Np(3)W(4)O(15))(H(2)O)(3)(SbW(9)O(33))(3)](18-) was the only neptunium containing species. In stark contrast to the NpO(2)(1+) chemistry, [BiW(9)O(33)](9-) readily oxidizes PuO(2)(1+) to PuO(2)(2+) yielding further evidence of the decreased stability of Pu(V)vs. Np(V). Np L(II)-edge XAFS measurement revealed very good agreement with single crystal diffraction data for the Np structural environment for [(Np(3)W(4)O(15))(H(2)O)(3)(MW(9)O(33))(3)](18-) (M = Bi, or Sb) in the solid state. There was also good agreement between coordination shells for [(Np(3)W(4)O(15))(H(2)O)(3)(BiW(9)O(33))(3)](18-) in the solid state and in solution, yielding further confirmation of the high stability of this particular cluster. 相似文献
308.
DiCarlo L Zhang Y McClure DT Reilly DJ Marcus CM Pfeiffer LN West KW 《Physical review letters》2006,97(3):036810
We report simultaneous measurement of shot noise and dc transport in a quantum point contact as a function of source-drain bias, gate voltage, and in-plane magnetic field. Shot noise at zero field exhibits an asymmetry related to the 0.7 structure in conductance. The asymmetry in noise evolves smoothly into the symmetric signature of spin-resolved electron transmission at high field. Comparison to a phenomenological model with density-dependent level splitting yields good quantitative agreement. 相似文献
309.
Kokkin DL Reilly NJ Morris CW Nakajima M Nauta K Kable SH Schmidt TW 《The Journal of chemical physics》2006,125(23):231101
A new band system of C(2), d (3)Pi(g)<--c (3)Sigma(u) (+) is observed by laser induced fluorescence spectroscopy, constituting the first direct detection of the c (3)Sigma(u) (+) state of C(2). Observations were made by laser excitation of c (3)Sigma(u) (+)(v(")=0) C(2), produced in an acetylene discharge, to the d (3)Pi(g)(v(')=3) level, followed by detection of Swan band fluorescence. Rotational analysis of this band yielded rotational constants for the c (3)Sigma(u) (+)(v(")=0) state: B(0)=1.9218(2) cm(-1), lambda(0)=-0.335(4) cm(-1) and gamma(0)=0.011(2) cm(-1). The vibrational band origin was determined to be nu(3-0)=15861.28 cm(-1). 相似文献
310.
Minasian SG Boland KS Feller RK Gaunt AJ Kozimor SA May I Reilly SD Scott BL Shuh DK 《Inorganic chemistry》2012,51(10):5728-5736
High-purity syntheses are reported for a series of first, second, and third row transition metal and actinide hexahalide compounds with equivalent, noncoordinating countercations: (Ph(4)P)(2)TiF(6) (1) and (Ph(4)P)(2)MCl(6) (M = Ti, Zr, Hf, Th, U, Np, Pu; 2-8). While a reaction between MCl(4) (M = Zr, Hf, U) and 2 equiv of Ph(4)PCl provided 3, 4, and 6, syntheses for 1, 2, 5, 7, and 8 required multistep procedures. For example, a cation exchange reaction with Ph(4)PCl and (NH(4))(2)TiF(6) produced 1, which was used in a subsequent anion exchange reaction with Me(3)SiCl to synthesize 2. For 5, 7, and 8, synthetic routes starting with aqueous actinide precursors were developed that circumvented any need for anhydrous Th, Np, or Pu starting materials. The solid-state geometries, bond distances and angles for isolated ThCl(6)(2-), NpCl(6)(2-), and PuCl(6)(2-) anions with noncoordinating counter cations were determined for the first time in the X-ray crystal structures of 5, 7, and 8. Solution phase and solid-state diffuse reflectance spectra were also used to characterize 7 and 8. Transition metal MCl(6)(2-) anions showed the anticipated increase in M-Cl bond distances when changing from M = Ti to Zr, and then a decrease from Zr to Hf. The M-Cl bond distances also decreased from M = Th to U, Np, and Pu. Ionic radii can be used to predict average M-Cl bond distances with reasonable accuracy, which supports a principally ionic model of bonding for each of the (Ph(4)P)(2)MCl(6) complexes. 相似文献