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991.
Baba M Kowaka Y Nagashima U Ishimoto T Goto H Nakayama N 《The Journal of chemical physics》2011,135(5):054305
Geometrical structures of the isolated benzene and naphthalene molecules have been accurately determined by using ultrahigh-resolution laser spectroscopy and ab initio calculation in a complementary manner. The benzene molecule has been identified to be planar and hexagonal (D(6h)) and the structure has been determined with accuracies of 2 × 10(-14) m (0.2 mA?; 1 A? = 1 × 10(-10) m) for the C-C bond length and 1.0 × 10(-13) m (1.0 mA?) for the C-H bond length. The naphthalene molecule has been identified to be symmetric with respect to three coordinate axes (D(2h)) and the structure has been determined with comparable accuracies. We discuss the effect of vibrational averaging that is a consequence of zero-point motions on the uncertainty in determining the bond lengths. 相似文献
992.
Yamazaki S Hosomura Y Matsuda I Hobara R Eguchi T Hasegawa Y Hasegawa S 《Physical review letters》2011,106(11):116802
We have succeeded in detecting metallic transport in a monatomic layer of In on an Si(111) surface, Si(111)-sqrt[7]×sqrt[3]-In surface reconstruction, using the micro-four-point probe method. The In layer exhibited conductivity higher than the minimum metallic conductivity (the Ioffe-Regel criterion) and kept the metallic temperature dependence of resistivity down to 10?K. This is the first example of a monatomic layer, with the exception of graphene, showing metallic transport without carrier localization at cryogenic temperatures. By introducing defects on this surface, a metal-insulator transition occurred due to Anderson localization, showing hopping conduction. 相似文献
993.
Cross-linked fluoroalkyl end-capped cooligomers possessing double decker-type aromatic silsesquioxane segments as core units
[RF-(Ar-SiSQ)
x
-(Co-M)
y
-RF] were prepared under mild conditions by the cooligomerizations of fluoroalkanoyl peroxide with the corresponding aromatic
silsesquioxane possessing bifunctional vinyl groups (Ar-SiSQ) and comonomers (Co-M) such as acryloylmorpholine (ACMO), N,N-dimethylacrylamide (DMAA) and N-(1,1-dimethyl-3-oxobutyl)acrylamide (DOBAA). Interestingly, these cross-linked fluorinated cooligomers thus obtained were
found to form the nanometer size-controlled nanoparticles with a good dispersibility in a variety of solvents including fluorinated
aliphatic solvents. These fluorinated cooligomeric nanoparticles were demonstrated to have red-shifted fluorescent emissions
related to the presence of aromatic silsesquioxane segments, compared with that of parent aromatic silsesquioxane, indicating
that each aromatic moiety in these nanoparticles can interact effectively with each other through the π–π stacking between
the aromatic moieties to afford the red-shifted fluorescent emissions. These fluorinated nanoparticles were also applied to
the surface modification of poly(methyl methacrylate) (PMMA) to exhibit not only a good oleophobicity imparted by fluorine
but also a fluorescent emission behavior related to aromatic silsesquioxane segments in nanoparticles on the modified PMMA
surface. More interestingly, cross-linked RF-(Ar-SiSQ)
x
-(DOBAA)
y
-RF cooligomeric nanoparticles interacted with fluorescein to give the corresponding fluorinated cooligomeric particles/fluorescein
nanocomposites in methanol. These fluorinated fluorescein nanocomposites were found to afford an extraordinarily enhanced
light absorption (λ
max = 441 nm), compared with that of fluoroalkyl end-capped DOBAA oligomer [RF-(DOBAA)
n
-RF] possessing no aromatic silsesquioxane segments. 相似文献
994.
Goto M Ishida S Ito Y Tamai N Matsuki H Kaneshina S 《Langmuir : the ACS journal of surfaces and colloids》2011,27(10):5824-5831
The bilayer phase transitions of dialkyldimethylammonium bromides (2C(n)Br; n = 12, 14, 16) were observed by differential scanning calorimetry and high-pressure light-transmittance measurements. Under atmospheric pressure, the 2C(12)Br bilayer membrane underwent the stable transition from the lamellar crystal (L(c)) phase to the liquid crystalline (L(α)) phase. The 2C(14)Br bilayer underwent the main transition from the metastable lamellar gel (L(β)) phase to the metastable L(α) phase in addition to the stable L(c)/L(α) transition. For the 2C(16)Br bilayer, moreover, three kinds of phase transitions were observed: the metastable main transition, the metastable transition from the metastable lamellar crystal (L(c(2))) phase to the metastable L(α) phase, and the stable lamellar crystal (L(c(1)))/L(α) transition. The temperatures of all the phase transitions elevated almost linearly with increasing pressure. The temperature (T)-pressure (p) phase diagrams of the 2C(12)Br and 2C(14)Br bilayers were simple, but that of the 2C(16)Br bilayer was complex; that is, the T-p curves for the metastable main transition and the L(c(2))/L(α) transition intersect at ca. 25 MPa, which means the inversion of the relative phase stability between the metastable phases of L(β) and L(c(2)) above and below the pressure. Moreover, the T-p curve of the L(c(2))/L(α) transition was separated into two curves under high pressure, and as a result, the pressure-induced L(c(2P)) phase appeared in between. Thermodynamic quantities for phase transitions of the 2C(n)Br bilayers increased with an increase in alkyl-chain length. The chain-length dependence of the phase-transition temperature for all kinds of transitions observed suggests that the stable L(c(1))/L(α) transition incorporates the metastable L(c(2))/L(α) transition in the bilayers of 2C(n)Br with shorter alkyl chains, and the main-transition of the 2C(12)Br bilayer would occur at a temperature below 0 °C. 相似文献
995.
Camarota B Goto Y Inagaki S Onida B 《Langmuir : the ACS journal of surfaces and colloids》2011,27(3):1181-1185
Oxygen sites in ethane-bridged and phenylene-bridged PMOs prepared using neutral templates in acidic conditions are characterized by means of XPS and FTIR spectroscopy of adsorbed pyrrole. Their electron donor ability is observed to be stronger than that of oxygens in pure amorphous silica of MCM-41 type and comparable to that reported for oxygen atoms in some alkali metal exchange zeolites. For pyrrole adsorbed on PMOs double interactions most probably occur, involving both silanols and electron donor sites at the surface. In the case of phenylene-bridged PMO preferential electron donor sites for interaction with pyrrole N-H group are aromatic rings rather than oxygens, as previously observed for adsorbed iodine. 相似文献
996.
Goto M Matsui T Tamai N Matsuki H Kaneshina S 《Colloids and surfaces. B, Biointerfaces》2011,84(1):55-62
The bilayer phase behavior of asymmetric phospholipids, palmitoylstearoylphosphatidylcholine (PSPC) and stearoylpalmitoylphosphatidylcholine (SPPC), with different vesicle sizes (large multilamellar vesicle (LMV) and giant multilamellar vesicle (GMV)) was investigated by fluorescence spectroscopy using a polarity-sensitive fluorescent probe Prodan under high pressure. The results were compared with those of a symmetric phospholipid, diheptadecanoyl PC (C17PC). The difference in phase transitions of the PSPC and SPPC bilayers and in thermodynamic quantities of the transitions was hardly observed between LMV and GMV as the case of the C17PC bilayer. On the other hand, the Prodan fluorescence showed clear differences between LMV and GMV of the asymmetric PC bilayers. From the second derivative of Prodan fluorescence spectra, the three dimensional image plots in which we can clearly see the location of Prodan in the bilayer membrane as blue valleys were constructed for LMV and GMV under high pressure. We revealed from the plots that the bilayer packing is significantly dependent on not only the vesicle size but also the acyl-chain asymmetry of PC molecule in addition to the phase states. It was found that the packing of the gel phases of the asymmetric PC bilayers is weaker than that of the symmetric PC bilayer, and the size of vesicle affects the packing of the interdigitated gel phase the most markedly among three gel phases. This study suggests that the Prodan molecules can detect the effect of vesicle size on the phase states for the asymmetric PC bilayers, and they become a useful indicator for various membrane properties, especially bilayer interdigitation. 相似文献
997.
Let (S,𝔫) be a 2-dimensional regular local ring and let I = (f, g) be an ideal in S generated by a regular sequence f, g of length two. Let I* be the leading ideal of I in the associated graded ring gr𝔫(S), and set R = S/I and 𝔪 = 𝔫/I. In Goto et al. (2007), we prove that if μ G (I*) = n, then I* contains a homogeneous system {ξ i }1≤i≤n of generators such that deg ξ i + 2 ≤ deg ξ i+1 for 2 ≤ i ≤ n ? 1, and ht G (ξ1, ξ2,…, ξ n?1) = 1, and we describe precisely the Hilbert series H(gr𝔪(R), λ) in terms of the degrees c i of the ξ i and the integers d i , where d i is the degree of D i = GCD(ξ1,…, ξ i ). To the complete intersection ideal I = (f, g)S we associate a positive integer n with 2 ≤ n ≤ c 1 + 1, an ascending sequence of positive integers (c 1, c 2,…, c n ), and a descending sequence of integers (d 1 = c 1, d 2,…, d n = 0) such that c i+1 ? c i > d i?1 ? d i > 0 for each i with 2 ≤ i ≤ n ? 1. We establish here that this necessary condition is also sufficient for there to exist a complete intersection ideal I = (f, g) whose leading ideal has these invariants. We give several examples to illustrate our theorems. 相似文献
998.
Akio Zama Yukiko Dokiya Motohiro Fukami Shiro Aizawa Miwako Hamachi Shozo Toda 《光谱学快报》2013,46(10):653-661
Flame Emission measurement of Na using an ordinary atomic absorption apparatus is performed in order to determine the concentration of Na in the surface water of the river Izumi, which is used for the irrigation of rice field in summer time. The effect of acids and K on Na emission are studied and found to be eliminated when the proper conditions and positions of the flame is chosen. The recovery ratio of 8 ppm and 200 ppm Na added to the well water and river water, respectively, are found to be within 92–105%. This method can be applied to the routine analysis of Na in river water samples. 相似文献
999.
1000.
Abstract Decay kinetics of Mn4+ luminescence in SrTiO3 and thermal stimulation of this luminescence (TSL) after low-temperature irradiation with light from the 355—520 nm region, have been investigated in the temperature range of 4.2—150K and 12—110K, respectively, for the first time. It is concluded that TSL glow peaks are associated with thermal release of carriers from shallow traps followed by Mn5+→Mn4+(2E) and/or Mn3+→Mn4+ (2E) charge transfer decay kinetics has been explained by considering trap energy levels taking part in the TSL process. 相似文献