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991.
P. Villemoes A. Wännström A. Arnesen R. Hallin F. Heijkenskjöld A. Kastberg C. Nordling O. Vogel 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1991,18(3):235-238
We report the first measurements of the hyperfine splitting of the fine structure levels 3d 5'4s a 5 S 2 and 3d 5 4p z 5 P 1,2,3 0 in singly ionised manganese in a collinear fast ion beam-laser experiment. The ions are excited by the intracavity frequency doubled output of a ring dye laser. The observed linewidth is sufficiently narrow to identify all hyperfine components of each fine structure level. 相似文献
992.
W. Krätschmer 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1991,19(4):405-408
At the beginning two remarks. One to the nomenclature: Fullerite does not name a specific substance; it names a solid entirely consisting of fullerenes, i.e. closed-cage all-carbon molecules. When our method of synthesis is applied, a solid is obtained in which C60 is the most abundant species. This material may thus be called C60-fullerite. The other remark regarding the production of fullerite: in view of the ease with which this could be achieved, I have the feeling that fullerene molecules must belong to a very frequently overlooked molecular species in carbon chemistry. Since the synthesis is simple and does not require many words to be described, I thought it might be interesting to tell how we came to make fullerite. 相似文献
993.
Zusammenfassung Das Verhalten von Polypropylen im elektrischen Wechselfeld wurde im Frequenzbereich von 0,15 kHz bis 300 kHz und im Temperaturbereich von –75 C bis +140 C untersucht. Es konnte sowohl ein Tieftemperaturdispersionsgebiet —-Absorption — als auch ein Hochtemperaturdispersionsgebiet —-Absorption — beobachtet werden. Die Untersuchungsergebnisse wurden, um die Breite des Dispersionsgebietes und die zugehörigen -Stufen zu bestimmen, nach demCole-Cole-Kreisbogengesetz analysiert. Aus dem Anstieg der Geraden: logf
max 1/T
K wurden sowohl für die- als auch fur die-Absorption die experimentellen Aktivierungsenergien berechnet. Eine Deutung der Ergebnisse wurde versucht. 相似文献
994.
Electron attachment spectroscopy is employed to study the formation of negative ions from the chloroethylenes. It is found that the resonances recently observed in the total electron scattering cross section are predominantly associated with the formation of Cl?. Only in tetrachloroethylene is a long-lived parent negative ion observed. 相似文献
995.
Ligand substitution of the mixed-metal clusters FeRu2(CO)12 and Fe2Ru(CO)12 with triphenylphosphine and trimethylphosphite has been studied. Mono- and di-substituted derivatives have been synthesized and characterized structurally. The following crystal and molecular structures are reported: Fe2Ru(CO)11PPh3: triclinic, space group P, a 9.203(2), b 11.903(3), c 15.117(4) Å, α 81.54(2), β 87.28(2), γ 66.72(2)°, Z = 2; Fe2Ru(CO)11P(OMe)3: orthorhombic, space group Pna21, a 17.220(5), b 14.572(4), c 8.708(6) Å, Z = 4, FeRu2(CO)11PPh3: monoclinic, space group P21/n, a 11.435(3), b 16.034(5), c 16.642(4) Å, β 93.35(2)°, Z = 4; FeRu2(CO)10(PPh3)2: orthorhombic, space group Pccm, a 14.854(4), b 17.180(7), c 16.786(12) Å, Z = 4.Ligand substitution is found to occur preferentially at the ruthenium centers of the FeRu2 and Fe2Ru clusters. Monosubstitution causes expansion of both of the clusters while the overall geometry is practically unchanged. Disubstitution of FeRu2(CO)12 causes contraction of the cluster and leads to a formation of carbonyl bridges. The structural trends have been interpreted in terms of electronic and packing effects of ligand substitution. The X-ray structures of Fe2Ru(CO)12 and FeRu2(CO)12 are not known; the ligand substitution studies indicate that Fe2Ru(CO)12 has the same structure as Fe3(CO)12, and that FeRu3(CO)12 does not have a Ru3(CO)12 structure as postulated previously from the IR studies. 相似文献
996.
1,3-Dipolar cycloaddition of nitrile oxides, generated from nitroethanol and nitroacetaldehyde derivatives 3, 21 and 22, respectively, and of benzonitrile oxide to 4-vinyldioxolanes 1, 2 gave ca 4:1 erythro/threo mixtures of corresponding isoxazolines. LAH reduction of erytho isoxazolines proceeded with similar (ca 4:1) selectivity to furnish protected ribo-amino-polyols 11, 15,19, DL- and D-lividosamines 31 and 33, respectively, as main products. The DL-lividosamine derivative 33 was obtained pure by crystallization. In the D-series, the corresponding ribo/arabino mixture D-31/D-32 was transformed to the known α-methyl D-lividosaminide D-37. 相似文献
997.
998.
Zusammenfassung 2,4,5-substituierte 4-Alkylamino-2H-imidazole entstehen mit guten Ausbeuten aus 2-Methyl-2,4-diaryl-imidazolin-3-thionen-(5) durch Umsetzung mit prim. bzw. sek. aliphatischen oder heterocyclischen Aminen in Benzol bei Rückflußtemperatur.
55. Mitt.:F. Asinger, E.-Chr. Witte undW. Schäfer, Ann. Chem., im Druck.
Teil der DissertationG. Kriebel, Techn. Hochschule Aachen, 1965. 相似文献
2.4.5-substituted 4-alkylamino-2H-imidazoles are formed in good yields by the reaction of 2-methyl-2.4-diaryl-3-imidazoline-5-thiones with prim. or sec. aliphatic or heterocyclic amines in boiling benzene.
55. Mitt.:F. Asinger, E.-Chr. Witte undW. Schäfer, Ann. Chem., im Druck.
Teil der DissertationG. Kriebel, Techn. Hochschule Aachen, 1965. 相似文献
999.
F. Asinger W. Schäfer H. Meisel H. Kersten A. Saus 《Monatshefte für Chemie / Chemical Monthly》1967,98(2):338-352
Zusammenfassung 2,2,5-Trisubstituierte Imidazolidin-thione-(4) lassen sich mittels Schwefels mit guten Ausbeuten zu Imidazolin-(3)-thionen-(5) dehydrieren. Hierüber sowie über einige Verbesserungen der bisher bekannten Synthesen für insbesondere 2,2,5-trisubstituierte Imidazolidin-thione-(4) wird berichtet.
Mitt.:F. Asinger, W. Schäfer undH. Triem, Mh. Chem.97, 1510 (1966).
Teil der Dissertation vonH. Meisel, Techn. Hochschule Aachen, 1963.
Teil der Dipl.-Arbeit vonHilde Kersten, Techn. Hochschule Aachen, 1963, und Teil der Dissertation vonHilde Kersten, Techn. Hochschule Aachen, 1965. 相似文献
Dehydration of 2.2.5-trisubstituted imidazolidine-(4)-thiones with elementary sulfur gives in good yields 3-imidazoline-(5)-thiones. This reaction and improved methods of the well known syntheses of especially 2.2.5-trisubstituted imidazolidine-(4)-thiones are described.
Mitt.:F. Asinger, W. Schäfer undH. Triem, Mh. Chem.97, 1510 (1966).
Teil der Dissertation vonH. Meisel, Techn. Hochschule Aachen, 1963.
Teil der Dipl.-Arbeit vonHilde Kersten, Techn. Hochschule Aachen, 1963, und Teil der Dissertation vonHilde Kersten, Techn. Hochschule Aachen, 1965. 相似文献
1000.
The e.m.f. of the cell Ag, AgCl/NaCl solution/sodium sensitive glass electrode was measured at 25°C. In pure water as a solvent, measured activity coefficients agree with tabulated osmotically determined values; hence, the ideality of the sodium response of the glass electrode is confirmed. Choosing a Tris – Tris. HCl buffer of the constant ionic strength 0,5M as a solvent, the applicability of HARNED'S rule was demonstrated. Conditions for measuring sodium ion concentrations with sodium sensitive glass electrodes are discussed. 相似文献