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991.
N. Momoshima N. Inoue Y. Takashima 《Journal of Radioanalytical and Nuclear Chemistry》1991,155(5):335-342
Loss of99Tc in seaweed during dry ashing has been investigated. Two kinds of brown seaweeds labeled with99Tc were ashed for 24 or 48 h at 400, 450 and 500 °C, showing no correlation between the loss of99Tc and species, temperature and time of ashing. The averaged recovery of99Tc was 91.0±4.0%, indicating that most of the99Tc in the seaweed was retained within the matrix of the ash which was obtained under general conditions of ashing. 相似文献
992.
Highly porous nanocomposites of zirconium dioxide and silicate are synthesised in an aqueous system from an inorganic salt of zirconium; the nanacomposites, with tailorable pore structures, exhibit superior performance as catalyst supports. 相似文献
993.
Kobayashi S Nakamura Y Maehara T Hamashima H Sasatsu M Asano K Ohishi Y Tanaka A 《Chemical & pharmaceutical bulletin》2001,49(9):1053-1060
We show that the topological significance of the gel mobility of cis-diamminedichloroplatinum(II) (DDP)-closed circular DNA (ccDNA) adducts decreases with reaction time, until a point at which it joins relaxed DNA, and that the mobility of the adducts increases again. There is no relationship between the relative length of the adducts and the gel mobility. Although the significance of the decrease of gel mobility is due to the unwinding of cis-DDP-DNA (or trans-DDP-DNA) adducts, the conformational significance of the subsequent increase in mobility is unclear. To elucidate the conformational significance for unwinding of the adducts, we measured the writhing number (Wk) of the adducts using electron microscopy and analyzed the topological states of cis-DDP (or trans-DDP) adducts based on the White rule, Lk=Wk+Tk. Where, Lk and Tk represent the linking and twisting number in the ring, respectively. From the data, we found that the Wk of cis-DDP-ccDNA adducts in comparison with trans-DDP-ccDNA adducts increases from a negative to a positive number with time. This suggests that cis-DDP plays a role in the change of the topological state of ccDNA. In the abstraction of platinum from the adducts with CN- ion, the differences in both topological states may explain why Pt in trans-DDP is abstracted more easily than in cis-DDP. To explain the abstraction of Pt ion, we also discuss the findings based on the thermodynamic cycle in a intermolecular crosslink model Pt(NH3)2(guanine)2(2+)-->Pt(CN)4(2-) using the Pt parametrized PM3 method. 相似文献
994.
M. Mohammad A. Y. Khan M. S. Subhani N. Bibi Safeer Ahmad Saba Saleemi 《Research on Chemical Intermediates》2001,27(3):259-267
Rate constants for the reaction of superoxide O-
2 with various substrates were obtained through stationary electrode polarography theory and technique. In solvent acetonitrile, the substrate and the rate constants of the reaction O-
2 + AH-
k2Product, are, AH = isopropanol (k2 < 0.01 M-1 s-1); ethanol (k2 = 1.42 × 102 M-1 s-1); methanol (k2 = 1.1 × 107 M-1 s-1), H2O (k2 = 1.0 × 105 M-1 s-1). In MeCN, O-2 was found to be rather unreactive towards glucose and acetone but it reacts with fructose and sucrose catalytically. However, in DMF2, O-
2reacts with glucose and fructose with k2 order of 105 M-1 s-1. The mechanism of the reaction of O-
2 with the substrates (AH) is proposed as O-
3 + AH k2O, AHk2
k-1 k [O2H + AH]-, k-2O2H + A- with k1 = 109 M-1 s-1 and k-1 = 108 -109 s-1. With these values of k-1 and k1, k k2(obs). The reversible E1/2 for O2 + e O-
2 in various solvents: MeCN, acetone, isopropanol, methanol, H2O were obtained either directly from the reversible voltammogram or from experimental voltammograms and the rate constants obtained (as above) using stationary electrode polargraphy theory; E1/2 being -0.82 (MeCN),-0.85 (acetone),-0.72 (isopropanol);-0.66 (MeOH),-0.56 (H2O) vs SCE. 相似文献
995.
Wagner G Pakhomova TB Bokach NA Fraústo Da Silva JJ Vicente J Pombeiro AJ Kukushkin VY 《Inorganic chemistry》2001,40(7):1683-1689
A novel method is reported for generation of the difficult-to-obtain (imine)Pt(II) compounds that involves reduction of the corresponding readily available Pt(IV)-based imines by carbonyl-stabilized phosphorus ylides, Ph3P=CHCO2R, in nonaqueous media. The reaction between neutral (imino)Pt(IV) compounds [PtCl4[NH=C(Me)ON=CR1R2]2] [R1R2 = Me2, (CH2)4, (CH2)5, (Me)C(Me)=NOH], [PtCl4[NH=C(Me)ONR2]2] (R = Me, Et, CH2Ph), (R1 = H; R2 = Ph or C6H4Me; R3 = Me) as well as anionic-type platinum(IV) complexes (Ph3PCH2Ph)[PtCl5[NH=C(Me)ON=CR2]] [R2 = Me2, (CH2)4, (CH2)5] and 1 equiv of Ph3P=CHCO2R (R = Me, Et) proceeds under mild conditions (ca. 4 h, room temperature) to give selectively the platinum(II) products (in good to excellent isolated yields) without further reduction of the platinum center. All thus prepared compounds (excluding previously described Delta4-1,2,4-oxadiazoline complexes) were characterized by elemental analyses, FAB mass spectrometry, IR and 1H, 13C[1H], 31P[1H] and 195Pt NMR spectroscopies, and X-ray single-crystal diffractometry, the latter for [PtCl2[NH=C(Me)ON=CMe2]2] [crystal system tetragonal, space group P4(2)/n (No. 86), a = b = 10.5050(10) A, c = 15.916(3) A] and (Ph3PCH2CO2Me)[PtCl3(NCMe)] [crystal system orthorhombic, space group Pna2(1) (No. 33), a = 19.661(7) A, b = 12.486(4) A, c = 10.149(3) A]. The reaction is also extended to a variety of other Pt(II)/Pt(IV) couples, and the ylides Ph3P=CHCO2R are introduced as mild and selective reducing agents of wide applicability for the conversion of Pt(IV) to Pt(II) species in nonaqueous media, a route that is especially useful in the case of compounds that cannot be prepared directly from Pt(II) precursors, and for the generation of systematic series of Pt(II)/Pt(IV) complexes for biological studies. 相似文献
996.
The stability constants of the Cu2+, Zn2+, Ni2+ and Mu2+ complexes of N-phenyl-o-methoxybenzohydroxamic acid at 30° in 50% v/v aqueous dioxan are: log K1 10·45, 8·16, 7·52, 6·33; log K2 8·90, 6·70, 6·01, 5·59 (for the ions in the order given). 相似文献
997.
J. Muntasell M. Barrio J. Font D. O. López J. Li. Tamarit M. A. Cuevas Diarte J. Guion M. Teisseire N. B. Chanh Y. Haget 《Journal of Thermal Analysis and Calorimetry》1991,37(10):2395-2398
The paper gives some comments about the potential use of plastic crystals in energy storage. The main point deals with the possibilities of binary solid solution formation. Three binary phase diagrams in the pentaerythritol series are commented on. 相似文献
998.
Sodium β-alumina crystals were elaborated by melting of a mixture of Na2CO3 and Al2O3 or by PbO flux evaporation and were studied by transmission electron microscopy. They exhibit regular planar defects lying in the {11.0} prismatic planes. These defects are described as antiphase boundaries for the cationic sublattice with fault vectors (such faults do not affect the anionic sublattice). As a consequence it would be interesting to study precisely the structure of the sodium β cationic lattice in the vicinity of the melting point. 相似文献
999.
M. SenŌ H. Noritomi Y. Kuroyanagi K. Iwamoto G. Ebert 《Colloid and polymer science》1984,262(9):727-733
The conformation of various basic poly (-amino acid)s was investigated by CD measurements in aqueous solutions containing bis (2-ethylhexyl)sodium sulfosuccinate (AOT) as well as in the AOT reversed micelles. The addition of AOT into an aqueous solution of poly(L-lysine) induces the conformational transition from coil to ordered structure, followed by aggregation. On the other hand, poly(L-lysine) assumes-structure in the reversed micelles at low wovalue (wo=[H2O]/[AOT]). Similarly to poly(L-lysine), poly(L-ornithine) takes an ordered structure in the aqueous solution containing AOT and-structure in the reversed micelles. In this case, however, these ordered structures are not so stable, compared with that of poly(L-lysine). Poly(L-arginine) undergoes the conformational transition from coil to helix by addition of AOT into the aqueous solution. Further addition of AOT allows transformation into-structure. Copoly(L-lysyl-L-leucine) with 63% leucine residue was shown to take a stable helical conformation even in pure water. In the reversed micelles, however, this ordered structure is significantly changed probably because the hydrophobic interaction among the leucyl residues is lowered in the reversed micelles. 相似文献
1000.
A primary cleavage of aliphatic ozonides by electron-impact, implying O? O and C? C bond breaking, is described. This mode of degradation, which is not observed for aromatic ozonides, is fav oured by electron releasing substituents. For the cis and trans 4-methyl-2pentene ozonides, the ionization potentials are 8.81 and 8.86 (±0.5) eV, respectively. Two formation thresholds are observed for the [RCHO2]+ion which are interpreted in terms of different modes of ozonide cleavage. 相似文献