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21.
22.
H. R. Lukens D. M. Fleishman R. L. Bramblett 《Journal of Radioanalytical and Nuclear Chemistry》1973,16(1):97-104
Measurement of uranium in highly enriched reactor fuel sticks has been achieved by elaboration of the method of Amiel. Calibration
of the method was achieved by three methods: comparison of dissolved sample with aqueous standard, comparison of sample, with
handcrafted standard stick, and the extrapolated-aliquot procedure. Precision and accuracy of<0.5% relative are achieved in<2
min measurement time on a production basis, Precisions of<0.1% relative are achieved in replicate measurements. 相似文献
23.
We present evidence for transitions between fluxoid wells of a SQUID due to cascaded, two-photon processes. Such transitions are evidenced by an anomalous dependence on the transition rate from the one-photon resonant level within the initial well, which cannot be explained by previously observed macroscopic resonant tunneling. These two-photon processes may be a significant source of decoherence in SQUID qubits subject to microwave radiation. 相似文献
24.
S. Lukens 《Fresenius' Journal of Analytical Chemistry》1915,54(1):72
Ohne Zusammenfassung 相似文献
25.
Leon A. Congdon A. B. Guss F. A. Winter A. Thiel Robert E. Sullivan Hiram S. Lukens und John H. Hastings 《Fresenius' Journal of Analytical Chemistry》1926,69(10):400-401
Ohne Zusammenfassung 相似文献
26.
27.
Dr. Ivana Radivojevic Jovanovic Dr. Colleen M. B. Gallagher Ramsey Salcedo Hossam Elshendidi Dr. Jacopo Samson Dr. Charles M. Drain Dr. Donna McGregor Dr. Wayne W. Lukens Jr. Dr. Benjamin P. Burton-Pye Dr. Lynn C. Francesconi 《欧洲无机化学杂志》2023,26(1):e202200507
Technetium-99 is a prevalent fission product from nuclear waste. The long half-life (211,000 yr) and environmental mobility of pertechnetate (TcO4−) render Tc particularly challenging to isolate and stabilize. Here we present two approaches for development of potential wasteforms using titanium dioxide, TiO2. Approach 1 is a low temperature chemical synthesis of TiO2 doped with Tc(IV) from TcO4− intended to mimic the Tc waste stream from the UREX family of separations and removes 98.5 % of the Tc, mainly present as edge-shared Tc(IV) pairs. Approach 2 utilizes TiO2 to photocatalytically reduce TcO4− to Tc(IV) stabilized on the surface of or within the TiO2 lattice. The %Tc removed from solution and adsorbed to TiO2 is pH dependent, with the maximum Tc(IV) adsorbed at pH 3–4 as either TcO2 or edge-sharing Tc(IV) octahedra. The Tc(IV)-TiO2 composites materials formed by both approaches are suitable for consolidation into a dense wasteform by Hot Isostatic Pressing (HIPing). 相似文献
28.
A procedure is described for the rapid estimation of concentration upper limits of elements not observed in a sample by routine instrumental reactor neutron activationanalysis. Experimental andtheoreticaljustifications of time-saving steps are given, and necessary precautions in the use of the procedure are discussed. Tables for use with the procedure are included. 相似文献
29.
Le Roux E Chabanas M Baudouin A de Mallmann A Copéret C Quadrelli EA Thivolle-Cazat J Basset JM Lukens W Lesage A Emsley L Sunley GJ 《Journal of the American Chemical Society》2004,126(41):13391-13399
The reaction of [Ta(=CHtBu)(CH2tBu)3] or [Cp*Ta(CH3)4] with a silica partially dehydroxylated at 700 degrees C gives the corresponding monosiloxy surface complexes [([triple bond]SiO)Ta(=CHtBu)(CH2tBu)2] and [([triple bond]SiO)Ta(CH3)3Cp*] by eliminating a sigma-bonded ligand as the corresponding alkane (H-CH2tBu or H-CH3). EXAFS data show that an adjacent siloxane bridge of the surface plays the role of an extra surface ligand, which most likely stabilizes these complexes as in [([triple bond]SiO)Ta(=CHtBu)(CH2tBu)2([triple bond]SiOSi[triple bond])] (1a') and [([triple bond]SiO)Ta(CH3)3Cp*([triple bond]SiOSi[triple bond])] (2a'). In the case of [(SiO)Ta(=CHtBu)(CH2tBu)2([triple bond]SiOSi[triple bond])], the structure is further stabilized by an additional interaction: a C-H agostic bond as evidenced by the small J coupling constant for the carbenic C-H (JC-H = 80 Hz), which was measured by J-resolved 2D solid-state NMR spectroscopy. The product selectivity in propane metathesis in the presence of [([triple bond]SiO)Ta(=CHtBu)(CH2tBu)2([triple bond]SiOSi[triple bond])] (1a') as a catalyst precursor and the inactivity of the surface complex [([triple bond]SiO)Ta(CH3)3Cp*([triple bond]SiOSi[triple bond])] (2a') show that the active site is required to be highly electrophilic and probably involves a metallacyclobutane intermediate. 相似文献
30.
Seaman LA Wu G Edelstein N Lukens WW Magnani N Hayton TW 《Journal of the American Chemical Society》2012,134(10):4931-4940
Reaction of UCl(4) with 5 equiv of Li(N═C(t)BuPh) generates the homoleptic U(IV) ketimide complex [Li(THF)(2)][U(N═C(t)BuPh)(5)] (1) in 71% yield. Similarly, reaction of UCl(4) with 5 equiv of Li(N═C(t)Bu(2)) affords [Li(THF)][U(N═C(t)Bu(2))(5)] (2) in 67% yield. Oxidation of 2 with 0.5 equiv of I(2) results in the formation of the neutral U(V) complex U(N═C(t)Bu(2))(5) (3). In contrast, oxidation of 1 with 0.5 equiv of I(2), followed by addition of 1 equiv of Li(N═C(t)BuPh), generates the octahedral U(V) ketimide complex [Li][U(N═C(t)BuPh)(6)] (4) in 68% yield. Complex 4 can be further oxidized to the U(VI) ketimide complex U(N═C(t)BuPh)(6) (5). Complexes 1-5 were characterized by X-ray crystallography, while SQUID magnetometry, EPR spectroscopy, and UV-vis-NIR spectroscopy measurements were also preformed on complex 4. Using this data, the crystal field splitting parameters of the f orbitals were determined, allowing us to estimate the amount of f orbital participation in the bonding of 4. 相似文献