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961.
Zusammenfassung Es wird ein isothermer Schnitt im System Nb2O5 -Li2O-Sc2O3 untersucht. Dabei wurde die neue Verbindung Li0.5Sc0.5Nb2O6 gefunden. Die Röntgenreflexionsaufnahmen ergaben unter Annahme eines orthorhombischen Gitters die Parameter a=1433.6/2/ pm, b=572.96/6/ pm und c=505.76/4/ pm.Bei 1453 K wurde der LiNbO3-Homogenitätsbereich bestimmt, der sich vom binären System Li2O-Nb2O5 bis zu 5 mol% Sc2O3 im Dreikomponentensystem erstreckt. Im Homogenitätsbereich wurde die Variation der Gitterkonstanten gemessen. Das Volumen der Elementarzelle nimmt mit steigendem Sc2O3-Gehalt zu.
An isothermal section was investigated in the system Nb2O5-Li2O-Sc2O3. The new compound Li0.5Sc0.5Nb2O6 was found The x-ray reflection pattern could be indexed with the assumption of an orthorhombic lattice with the parameters of a=1433.6(2) pm, b=572.96(6) pm, c=505.76(4) pm.The LiNbO3-homogeneity range was determined at 1453 K. It extends from the binary Li2O-Nb2O5 to 5 mole-% Sc2O3 in the ternary system. The variation of the lattice constants of LiNbO3 was measured in the homogeneity range. The volume of the unit cell increases with increasing content of Sc2C3.

Nb2O5-Li2O-Sc2O3, Li0,5 Sc0,5Nb2O6. , $ = 1433,6/2/ , =572,96/6/ =505,76/4/ . 1453 LiNbO3, $ Li2O-Nb25 $ 5 %. $ . .
  相似文献   
962.
Temperature programmed reduction (TPR) has been used to study the redox behavior of Ni(II) ions in nickel sodium mordenite (NiNaM) and decationated nickel mordenite (NiHM). The TPR profiles suggest that Ni(II) ions occupy nonequivalent sites with different cooridination states in the mordenite. The reducibility of Ni(II) depends strongly on the zeolite acidity.
() NiII NiNaM NiHM. . .
  相似文献   
963.
A simple and sensitive method for determination of benzodiazepines in plasma has been developed using high-performance liquid chromatography in a reverse-phase mode. The method is illustrated by application to plasma samples containing diazepam and N-desmethyldiazepam at concentrations which would be encountered during therapy, with limits of detection of 10 ng/ml and 2 ng/ml for diazepam and N-desmethyldiazepam, respectively.  相似文献   
964.
N,N-Dimethyl diethyl, dipropyl, dibutyl, and N-monoisopropylaminoaphthylenesulfonyl derivatives of melanotropin inhibiting factor (MIF) and its metabolites were prepared, and their chromatographic behavior was investigated with thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC), using five solvent systems on polyamide layers and ten solvent systems on muBondapak C18 and muBondapak phenyl columns. A mixture of MIF and its metabolites derivatized with Dns chloride was adequately resolved by two-dimensional chromatography on polyamide layer with solvent systems, formic acid-water (3:97) and benzene-acetic acid (9:1). Bns-MIF and its metabolites were separated with muBondapak C18 column with the solvent system acetonitrile-0.01 M sodium sulphate buffer, pH 7 (50:50). They were separated into five groups: Gly and Bns acid; Pro-Leu, Leu-Gly and Leu; Pro; Gly-NH2; and MIF. The alkylaminonaphthylenesulfonyl derivates had strong fluorescence, which permitted their detection at the level of 10(-11) to 10(-9) mol. Dns-MIF and its derivatives had the lowest detectable amounts. HPLC with the aid of the Dns derivation is reliable and fast, and is the preferable method for study of neuropeptide breakdown.  相似文献   
965.
Exposure of ent-kaura-2,16-dien-19-ol (1) or its succinate (2) to resuspended mycelia of G. fujikuroi has produced a complex mixture of acids which after methylation gave the esters of two C19 (24) and (30) and five C20 gibberellins (4, 11, 20, 32 and 33). The triester (32) and the lactone ester (24) have been prepared before from the esters of gibberellin A13 (8) and gibberellin A4 (26) respectively. The structures of the other metabolites were assigned on spectroscopic data and by chemical transformations. Thus the lactone diester (4) has been converted to the known keto triester (6). The epoxide (11) has been related to gibberellin A14 (14) and the aldehyde (33) has been related to gibberellin A13 trimethyl ester (8) by way of the triol (34). Selective de-epoxidation of the 16,17-epoxy function in diepoxides has provided a route from the dienes (20 and 24) to the epoxides (11 and 30) respectively, but not from the ester of gibberellin A5 (23) to that of gibberellin A6 (29). On the other hand the latter can be obtained by epoxidation of gibberellin A5 methyl ester trifluoroacetate. Backfeeding experiments carried out with the epoxy diacid (12), the diene diacid (21) and the derived diol (39) indicate pathways connecting the various metabolites. The natural gibberellins A5 and A6 were shown to be formed in some of the backfeeding experiments.  相似文献   
966.
RECOVERY OF HAEMOPHILUS INFLUENZAE FROM ULTRAVIOLET AND X-RAY DAMAGE   总被引:14,自引:0,他引:14  
Abstract— Results of experiments on reactivation of ultraviolet (u.v.)-irradiated Haemophilus influenzae and cellular reactivation of u.v.-damaged transforming deoxyribonucleic acid (DNA) and bacteriophage are reported. Liquid-holding recovery (LHR) is small for the u.v.-sensitive mutant BC100 which, relative to the wild type, also has greatly reduced host-cell reactivation (HCR) of u.v.-inactivated phage, and competent cultures show reduced competent cell reactivation (CCR) of u.v.-inactivated transforming DNA. BC100 cells can be transformed with DNA isolated from the wild type strain Rd to a u.v. resistance similar to that of Rd, and irradiation of the DNA reduces the transformation frequency for this marker (uvr). The u.v.-resistant mutant BC200 displays very little LHR under the usual conditions where reactivation occurs after plating. The colony-forming ability (cfa) of irradiated BC200 is greater than that of Rd, but HCR and CCR are the same on this mutant as on the wild type. The major difference between Rd and BC200 is the enhanced u.v. survival of cfa of the latter. It was determined that this difference reflects cell lysis of irradiated Rd and lack of lysis in BC200 cultures. That lysis is closely correlated with damage to the bacterial chromosome is suggested by the finding that the lytic response of Rd (as determined turbidimetrically) can be negated by the liquid-holding procedure, but lysis of BC100 (which lacks comparable DNA-repair ability) can be only partially inhibited by this procedure. LHR occurs when post-plating dark recovery is incomplete, is temperature-sensitive, and occurs unimpeded when post-u.v. protein synthesis is inhibited by chloramphenicol. It is suggested that enzymatically catalyzed reactivation of DNA occurs or is initiated during liquid-holding of u.v.-irradiated H. influenzae Rd and that the necessary enzyme(s) exists prior to appearance of u.v. lesions in the DNA. Results are reported for X-ray inactivation of transforming DNA as assayed on BC100, Rd and BC200 and of the cfa of the three strains.  相似文献   
967.
The chain-scission reaction which occurs in copolymers of styrene and acrylonitrile has been studied at temperatures of 262, 252, and 240°C. Under these conditions volatilization is negligible, and chain scission can be studied in virtual isolation. At 262°C three kinds of chain scission are discernible, namely, at weak links which are associated with styrene units, “normal” scission in styrene segments of the chain and scission associated with the acrylonitrile units. The rate constants for normal scission and scission associated with acrylonitrile units are in the ratio of approximately 1 to 30. The molecular weight of the copolymer has no effect on the rates of scission. At 252°C the same general behavior is observed for the copolymers containing up to 24.9% acrylonitrile. The 33.4% acrylonitrile copolymer is anomalous, however. At 240°C the trends observed at 262°C appear to break down completely although individual experiments are quite reproducible. This behavior at the lower temperatures is believed to be associated with the fact that the melting points of the various copolymers are in this temperature range. Thus the viscosity of the medium, which should be expected to have a strong influence on the chain scission reaction, will be changing rapidly with temperature, copolymer composition, and molecular weight in this temperature range.  相似文献   
968.
969.
The dihydronaphthodiphenazine ofKehrmann, which is according toBadger andPettit reported to be 14-o-aminophenyl-13,14-dihydro-5,8,13,14-tetraaza-6,7-benzopentaphene, is N-(o-aminophenyl)-benzo[a]phenazin-5-amine. This was proved by chemical and spectroscopic investigations. The structures of the derivatives prepared byBadger andPettit are also corrected and the acetylation processes are cleared up.  相似文献   
970.
Thermogravimetry (TG), differential thermal analysis (DTA) and X-ray diffraction studies of antimony(III) oxide, (Sb2O3), in air, nitrogen and argon atmospheres have been made. In air Sb2O3 becomes oxidized to Sb2O4 above 510°. The oxidation reaction proceeds in two stages as revealed by the TG and DTA curves. The behaviour of Sb2O3 is similar in both N2 and Ar. Sb2O3 remains unaffected up to 430°, above which there is a slow, and continuous mass loss up to 550°. Above 550° Sb2O3 volatilizes resulting in an enormous weight loss. X-ray studies of the sublimate and the residue indicate the former to be the cubic form of Sb2O3 (Senarmontite) while the residue is the orthorhombic (Valentinite) structure. From the DTA curves in air, N2 and Ar, the transition temperature for the cubic to the orthorhombic modification has been estimated to be around 610°.  相似文献   
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