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241.
Pentacene have recently become the subject of intense studies due to their physical properties which follow from the states
of their outer-shell electrons that are able to take part in molecule bonding. The symmetry of these molecules provides the
classification of quantum states according to the group theory method. In this paper, we apply a molecular state-space factorization
scheme for the classification of pentacene molecules based on the structure of their electron states. 相似文献
242.
In Hwan Jung Young Kwan Jung Jonghee Lee Jong‐Hwa Park Han Young Woo Jeong‐Ik Lee Hye Yong Chu Hong‐Ku Shim 《Journal of polymer science. Part A, Polymer chemistry》2008,46(21):7148-7161
We synthesized two fluorene‐based copolymers poly[(2,5‐bis(4‐hexylthiophen‐2‐yl)thiazolo[5,4‐day]thiazole‐5,5′‐diyl)‐alt‐(9,9′‐dioctylfluorene‐2,7‐diyl)] ( PF‐TTZT), and poly[(5,5′‐bis(4‐hexylthiophen‐2‐yl)‐2,2′‐bithiazole‐5,5′‐diyl)‐alt‐(9,9′‐dioctylfluorene‐2,7‐diyl)] (PF‐TBTT), which contain the electron‐withdrawing moieties, thiazolothiazole, and bithiazole, respectively. Through electrochemical studies, we found that these two polymers exhibit stable reversible oxidation and reduction behaviors. Moreover, the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels of PF‐TBTT are lower than those of PF‐TTZT, and the bandgap of PF‐TBTT is smaller than that of PF‐TTZT. Thus the bithiazole moiety in PF‐TBTT is more electron‐withdrawing than the thiazolothiazole moiety in PF‐TTZT. Light‐emitting devices with indium tin oxide (ITO)/poly(3,4‐ethylene dioxythiophene):poly(styrenesulfonate)(PEDOT)/polymer/bis(2‐methyl‐8‐quinolinato)‐4‐phenylphenolate aluminum (BAlq)/LiF/Al configurations were fabricated. The performance of the PF‐TBTT device was found to be almost three times better than that of the PF‐TTZT device, which is because electron injection from the cathode to PF‐TBTT is much easier than for PF‐TTZT. We also investigated the planarity and frontier orbitals of the electron donor‐acceptor (D‐A) moieties with computational calculations using ab initio Hartree–Fock with the split‐valence 6‐31G* basis set. These calculations show that TBTT has a more nonplanar structure than TTZT and that the bithiazole moiety is more electron‐withdrawing than thiazolothiazole. These calculations are in good agreement with the experimental results. © Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7148–7161, 2008 相似文献
243.
Young Kwan Jung Hyoseok Kim Jong‐Hwa Park Jaemin Lee Sang Kyu Lee Yoon Sup Lee Hong‐Ku Shim 《Journal of polymer science. Part A, Polymer chemistry》2008,46(11):3573-3590
Several fluorene copolymers containing isothianaphthene units ( P1 , P2 , and P3 ) or similar derivatives ( P4 and P5 ) have been synthesized by Pd‐catalyzed Suzuki polymerization. The monomers containing isothianaphthene were prepared by a ring‐closure reaction with Lawesson's reagent. Strong photoluminescence (PL) quenching in the film state was observed for P1 and P2 , which was mainly due to the enhanced quinoid character formed by introducing the isothianaphthene unit. Their energy levels of the compounds were determined using cyclic voltammetry. Among the polymers tested, the polymer containing both an isothianaphthene and a selenophene unit, P2 , showed the smallest band gap of 1.85 eV. The influence of structural variation on the band gap of the polymer chains was further investigated by optimizing the geometries of several model monomers. Our results based on the optical and electrochemical properties combined with theoretical calculations showed that polymers containing isothianaphthene have small band gaps, rigid conformations, and strong tendencies to aggregation. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3573–3590, 2008 相似文献
244.
245.
M will be a compact connected n-dimensional Riemannian manifold. If M contains a closed connected k-dimensional, 2 k < n, minimal immersed submanifold of M, we define the kth isoperimetric number of M, Ñ
k
(M), as the infimum of the volumes of all such submanifolds. We obtain a number of interesting estimates for Ñ
k
(M), for both general and special manifolds, which appear to be new.Next we turn to isometric actions and a 1931 theorem of M. H. A. Newman involving the size of orbits of group actions on manifolds. We introduce the higher Newman numbers N
k
(M), 1 k n. Roughly speaking, if M admits isometric actions of compact connected Lie groups with k-dimensional principal orbits, N
k
(M) is defined as the infimum over all such actions of the maximum volume of all maximal dimensional orbits. We observe that N
k
(M) Ñ
k
(M), 2 k < n, provided N
k
(M) is defined; hence our prior estimates for the isoperimetric numbers of M apply directly to the higher Newman numbers.As a best possible candidate we conjecture that N
k
(M) vol S
k
(i(M)/), 1 k n, where i(M) denotes the radius of injectivity of M and S
k
(i(M)/) denotes the standard k-sphere of radius i(M)/. We verify the conjecture for various special cases. We conclude the paper by studying Newman's theorem for compact connected Lie groups with invariant metrics and obtaining a lower bound for the size of small subgroups. 相似文献
246.
247.
V. Foltýnová L. Voska C. Povýšil J. Kučera N. Pilecká M. Rakovič 《Journal of Radioanalytical and Nuclear Chemistry》1995,201(6):477-480
Sodium was determined by the use of instrumental neutron activation analysis in sections of compact bone, red marrow and yellow marrow to check possible effects of shoft tissues in the bone when determining the Na/Ca ratio in sections of the undecalcified bone tissue. The results indicated that this ratio actually reflects the sodium content in the bone mineral, the contribution from the soft tissues being two orders of magnitude lower. 相似文献
248.
A new class of fluorescence sensors for ammonium and organoammonium ions has been disclosed. One of the sensors, an alaninol-derived tripodal oxazoline (1a) shows significant fluorescence enhancement upon binding NH(4)(+) but little response toward K(+), Na(+), and Mg(2+) ions. Owing to its chiral environment, a phenylglycinol-derived tripodal oxazoline (1b) shows chiral discrimination in fluorescence upon binding enantiomeric guests. [reaction: see text] 相似文献
249.
The boundary effect on electrophoresis is investigated by considering a finite cylindrical particle moving along the axis of a long cylindrical pore under conditions of low surface potential and weak applied electric field. The influence of the thickness of the double layer, the aspect ratio of a particle, the ratio particle radius/pore radius, and the charged conditions of the surfaces of the particle and pore on the electrophoretic behavior of a particle are investigated. We show that the effect of the aspect ratio of a particle on its electrophoretic behavior for the case where the particle is charged and the pore is uncharged is larger than that for the case where the particle is uncharged and the pore is charged. Also, depending on the parameters chosen, increasing the aspect ratio of a particle can either promote or hinder its movement, which is not reported in previous studies, and can play a role in electrophoresis measurements. Because both the electric and the flow fields in the gap between the particle and the pore are mediated by those near the top and the end of the particle, the end effect is large when the double layer is thick. 相似文献
250.
Ilona Šperlingová Ludmila Dabrowská Vladimír Stránský Jan Kučera Miloň Tichý 《Accreditation and quality assurance》2006,11(5):231-235
The candidate reference material (RM) was prepared by freeze-drying pooled urine samples obtained from healthy persons occupationally exposed to toluene. Homogeneity testing yielded no significant differences of urinary concentrations of o-cresol and phenol in 15 randomly selected units of RM. Stability testing showed no significant changes of concentrations of the above analytes over a period of 6 months. Property (pre-certified) values of phenol and o-cresol concentrations and their uncertainties (9.06±0.47 mg l−1 and 1.03±0.06 mg l−1, respectively) were estimated from results of a small-scale interlaboratory comparison in which two laboratories participated using four different analytical methods. 相似文献