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51.
Methacrylate monolithic stationary phases were produced in fused-silica chips by UV initiation. Poly(butyl methacrylate-co-ethylene dimethacrylate) (BMA) and poly(lauryl methacrylate-co-ethylene dimethacrylate) (LMA) monoliths containing 30, 35 and 40% monomers were evaluated for the separation of peptides under gradient conditions. The peak capacity was used as an objective tool for the evaluation of the separation performance. LMA monoliths of the highest density gave the highest peak capacities (≈40) in gradients of 15 min and all LMA monoliths gave higher peak capacities than the BMA monoliths with the same percentage of monomers. Increasing the gradient duration to 30 min did not increase the peak capacity significantly. However, running fast (5 min) gradients provides moderate peak capacities (≈20) in a short time. Due to the system dead volume of 1 μL and the low bed volume of the chip, early eluting peptides migrated over a significant part of the column during the dwell time under isocratic conditions. It was shown that this could explain an increased band broadening on the monolithic stationary phase materials used. The effect is stronger with BMA monoliths, which partly explains the inferior performance of this material with respect to peak capacity. The configuration of the connections on the chip appeared to be critical when fast analyses were performed at pressures above 20 bar. 相似文献
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Qiang Wang Kok Hwa Lim Shuo-Wang Yang Yanhui Yang Yuan Chen 《Theoretical chemistry accounts》2011,128(1):17-24
Atomic carbon is a key intermediate interacting with transition metal clusters during the growth of carbon nanotube (CNT). Present density functional calculations studied the initial carbon adsorption on four Ni nanoclusters (N13, N15, N38, and N55). Our results show that carbon atoms preferentially adsorb on high-coordination sites, and carbon adsorption energies are larger on smaller Ni clusters. Ni cluster reconstruction plays an important role in creating more stable subsurface adsorption sites. The migration of adsorbed carbon atom on the surface threefold hollow site into the underlying interstitial subsurface positions is thermodynamically and kinetically feasible. The results indicate that the investigation of CNT growth mechanism should include both surface and subsurface carbon atoms, coupled with surface reconstruction of Ni nanoclusters. 相似文献
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Wai‐Yeung Wong Suk‐Yue Poon Jian‐Xin Shi Kok‐Wai Cheah 《Journal of polymer science. Part A, Polymer chemistry》2006,44(16):4804-4824
A series of blue‐light‐emitting oligo(fluorenyleneethynylenesilylene)s (OFESs) of the general formula HC?CRC?C(EC?CRC?C)mEC?CRC?CH (E = SiPh2, SiMe2, or SiMe2? SiMe2; m = 0–2; R = 9,9‐dihexylfluorene‐2,7‐diyl) and their phosphorescent platinum‐containing oligoynes and polyynes were synthesized and characterized. The solution properties and regiochemical structures of this new structural class of organosilicon‐based polyplatinayne polymers {trans‐[? Pt(PBu3)2C ?CRC?C(EC?CRC?C)mEC?CRC?C? ]n} were studied with IR and NMR (1H, 13C, 29Si, and 31P) spectroscopy. The optical absorption and photoluminescence spectra of these metallopolymers were examined and compared with their discrete oligomeric model complexes. Our studies led to a novel approach of using the sp3‐silyl moiety as a conjugation interrupter to limit the effective conjugation length in metal polyynes, which could boost the phosphorescence decay rates essential for light‐energy harvesting from the triplet excited state. The influence of the heavy platinum atom and the group 14 silyl unit possessing different side‐group substituents on the thermal and phosphorescence properties was investigated in detail. We also established the goal of studying the evolution of the lowest singlet and triplet excited states with chain length m of OFESs and the nature of E in these metallopolymers. This work indicated that the phosphorescence emission efficiency harnessed through the heavy‐atom effect of platinum in the main chain did not change very much with oligomer chain length m but generally decreased with the E group in the order SiMe2 > SiMe2? SiMe2 > SiPh2. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4804–4824, 2006 相似文献
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Summary Mixed-ligand complex formation of copper(I) with 2,2,2-terpyridine (terpy) and various biologically significant sulfurcontaining amino acids, L [L = cysteine, penicillamine,N-acetylcysteine andN-acetylpenicillamine] was investigated. WithN-acetylcysteine andN-acetylpenicillamine, copper(I) complexes [Cu(terpy)L]HCl have been isolated and characterised. The amino acid in each case bonds to the copper(I) through the sulfur atom only. These complexes are readily oxidised to the corresponding copper(II) complexes which contain a CuII-S(mercaptide) bond as demonstrated by the (S)CuII LMCT at 420 nm. The e.p.r. and electronic spectroscopic results are consistent with a distorted octahedral structure. Reactions of copper(I) with terpy and cysteine/ penicillamine in weakly acidic medium produce complexes containing two different copper(II) centres. From a strongly acidic medium, a binary copper(I) terpyridine complex is obtained instead and is shown from i.r. spectral absorptions to contain a protonated pyridyl ring. 相似文献
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