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81.
82.
Hitoshi Osawa Toshiaki IwazumiHiroko Tokoro Shin-ichi OhkoshiKazuhito Hashimoto Hironobu ShojiEiju Hirai Tetsuya NakamuraSusumu Nanao Yasuhito Isozumi 《Solid State Communications》2003,125(5):237-241
The thermal phase transition of RbMnFe(CN)6 has been observed by Mn and Fe 3p-1s X-ray emission spectroscopy (XES) and 1s X-ray absorption spectroscopy (XAS). The thermal variations of the spin states and the valences of Mn and Fe were determined to be Mn2+(S=5/2)-NC-Fe3+(S=1/2) for the high-temperature (HT) phase and Mn3+(S=2)-NC-Fe2+(S=0) for the low-temperature (LT) phase. These transitions are thus caused by charge transfer between Mn and Fe. The temperature dependences of Mn and Fe 3p-1s XES and 1s XAS were observed as the composition of the spectra of the HT and LT phases. The ratios of the HT component in each spectrum show good agreement with the thermal transition curves observed with magnetic susceptibility measurements. 相似文献
83.
84.
The energy spectrum and α-spectroscopic factors of40Ca are calculated by using an α+36Ar orthogonality condition model. Overall agreement is obtained with the experimental data. The model successfully produces the parity-doubletK π=O + and O? α+36Ar cluster bands. It is shown that the coexistence and interference of α-cluster states and shell-model states are indispensable to understand the structure of40Ca. 相似文献
85.
RuS2 nanoparticles, smaller than 3 nm in diameter, were prepared by H2S gas injection into the AOT/isooctane reverse micellar solution containing RuCl3 aqueous solution. The nanoparticle size was found to be independent of the Wo (water content) value of the reverse micellar system, as shown by TEM observation. The recovery and immobilization of the RuS2 nanoparticles from reverse micelles onto thiol-modified polystyrene particles (PSt-SH) were successfully carried out, by the addition of PSt-SH into the reverse micellar solution under conditions of mild stirring. The resulting composites, PSt-RuS2, showed photocatalytic activity for H2 generation form aqueous solution containing 2-propanol and Na2SO3 as sacrificial electron donors. 相似文献
86.
Seiji Yamaguchi Eriko Hamade Hajime Yokoyama Yoshiro Hirai Shunsaku Shiotani 《Journal of heterocyclic chemistry》2002,39(2):335-339
Birch reduction of four furopyridines 1a‐d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a‐d , vinylpyridinols 3b,d , and ethylpyridinols 4a‐d , and the reduction of the furan ring, giving dihydrofuropyridine 5c,d. 相似文献
87.
Ram Sharma Tiwaree Kyeoung-scik Cho Mitsgyo Hirai Makoto Shoda 《Applied biochemistry and biotechnology》1992,32(1-3):135-148
Biological deodorization of dimethyl sulfide (DMS) was studied using nine unwoven fabrics as the carriers of microorganisms in a laboratory-scale deodorizing system. The activated carbon fabric FN-200CF-15 was the best packing material compared with other packing materials used, on the basis of removal rate. The maximum removal rate (Vm), evaluated by using Michaelis-Menten equation, was 2.28 g-Skg-dry fab.-1 day-1 in this fabric biofilter. The critical load of DMS in this fabric biofilter was dependent on space velocity (SV), determined as 0.78 and 0.66 g-Skg-dry fab.-1 at SV 100 and 150 h-1, respectively. Strain IM1 isolated from the carbon fabric FN-200CF-15 biofilter in modified Waksman (MW) medium successfully degraded DMS as well as hydrogen sulfide (H2S), methanethiol (MT), and dimethyl disulfide (DMDS) in batch test. The DMS removal rates (g-S cell-1h-1) by this strain measured in batch culture and calculated in FN-200CF-15 biofilter by the cell numbers appeared in MW medium were found almost equal, indicating that strain IM1 may be the dominant microorganism in this biofilter. 相似文献
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89.
Yasuhiro Shiraishi Yugo Furubayashi Go Nishimura Takayuki Hirai 《Journal of luminescence》2007,127(2):623-632
Dinuclear lanthanide (Ln=Tb3+ or Eu3+) complexes (Ln2L2) of two octadentate macrocyclic polyaminopolycarboxylic ligands connected through a benzophenone (BP) moiety (L2) have been synthesized. Sensitized luminescence properties of Ln2L2 in water have been studied in comparison to those of BP-conjugated mononuclear Ln complexes (LnL1). The luminescence intensity of Tb2L2 is lower than that of TbL1 because of lower triplet quantum yield of the BP moiety. In contrast, Eu2L2 shows higher intensity than EuL1. For both Eu complexes, energy level of triplet excited-state BP (3BP*) is only 3 kJ mol−1 higher than that of 5D2 excited-state of Eu3+. The 5D2 state formed by a triplet-energy transfer (TET) from 3BP* is therefore deactivated by a back energy transfer (BET) to the ground-state BP, resulting in low luminescence intensity of EuL1. In contrast, within Eu2L2, TET from 3BP* to 5D0 state of two Eu3+ ions is accelerated, thus leading to higher luminescence intensity. Another notable feature of Eu2L2 is the luminescence quantum yield independent of its concentration. In contrast, for EuL1 system, an intermolecular BET occurs from 5D2 state of Eu3+ to the ground-state BP conjugated to another EuL1 complex, resulting in a yield decrease with the concentration increase. 相似文献
90.