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61.
G. Rasulić Lj. Milanović S. Jovanović G. Novohatni V. Krivokuća Z. Marjanović 《Journal of Thermal Analysis and Calorimetry》1985,30(1):73-82
A study was made of the changes in the active component of a commercial catalyst for methane reforming by means of steam, as a function of its duration of use and of its position in an industrial reactor. The samples for examination were taken after 3, 8, 9 and 20 months of catalyst use, and from seven different levels in the reformer tube, ranging from the top to the bottom.DTA, TG, IR spectroscopy, X-ray diffraction and surface area determination were used to follow the catalyst changes.
Zusammenfassung Veränderungen der aktiven Komponente eines kommerziellen Katalysators zur Methanreformierung mittels Wasserdampf wurden in Abhängigkeit von der Betriebsdauer und der Lage im industriellen Reaktor untersucht. Proben für die Untersuchung wurden nach 3-, 8-, 9- und 20-monatiger Betriebsdauer aus 7 verschiedenen Höhen vom Boden bis zum Kopf des Reformer-Rohres entnommen. Veränderungen des Katalysators wurden mittels DTA, TG, IR-Spektroskopie, Röntgendiffraktometrie und Oberflächenmessungen verfolgt.
, - , @2 . 3, 8, 9 20 -, -. , , , , , .相似文献
62.
A study was made of the difference occurring in ammonium nitrate during investigation by DTA and by DSC. The results show that the DTA of ammonium nitrate (p.a.) is accompanied by the crystal transformation IV III II I and melting. During DSC investigation of the same ammonium nitrate samples, the salt undergoes the transformations IV III and IV II in parallel; then follow the crystal transformations III II I and melting. The investigation conditions and the history of the samples do not essentially influence the crystal transformations during thermal analysis.
Zusammenfassung Bei DTA und DSC von Ammoniumnitrat zu beobachtende Unterschiede wurden untersucht. Bei der DTA von p.a. Ammoniumnitrat verlaufen die Kristallumwandlungen IV III II I sowie der Schmelzvorgang. Während der DSC der gleichen Ammoniumnitratproben verlaufen die Übergänge IV III und IV II parallel, worauf die Kristallumwandlungen III II I und der Schmelzvorgang folgen. Die experimentellen Bedingungen und die Vorgeschichte der Proben hat keinen wesentlichen Einfluß auf die während der thermischen Analyse verlaufenden Kristallumwandlungen.
. ( ..) IV III II I . , IV III IV II - , III II ar I . .相似文献
63.
Summary Adsorption properties of activated carbon cloth were investigated by gas-solid chromatography. Retention of several organic
compounds was measured in the temperature range from 200 to 250°C. The gas/solid distribution coefficients and the related
thermodynamic function of adsorption at zero surface coverage were determined. The obtained experimental data were used to
explain the adsorbent-adsorbate interaction. 相似文献
64.
Gertraud Chiste Helmut Egg Klemens Kraus Elisabeth Pipitz Elisabeth Spanyar 《Monatshefte für Chemie / Chemical Monthly》1991,122(6-7):537-544
Summary A new method for the synthesis of 1,2-diaryl-1,2-dihydro-5-methyl-3H-pyrazol-3-ones3 and 4-acetyl-1,2-diaryl-1,2-dihydro-5-methyl-3H-pyrazol-3-ones5 is presented. The reaction of 4,4-disubstituted 1,2-diarylhydrazines1 with acetic anhydride in the presence of an equimolar amount of 4-(dimethylamino)pyridine leads to mixtures of the corresponding acetyl derivatives2 and3. Under the same conditions, 2,2-disubstituted 1,2-diarylhydrazines yield mixtures of3 and5.
4-(Dimethylamino)pyridin-katalysierte Reaktion von 1,2-Diarylhydrazinen mit Essigsäureanhydrid
Zusammenfassung Eine neue Methode zur Synthese von 1,2-Diaryl-1,2-dihydro-5-methyl-3H-pyrazol-3-onen3 und 4-Acetyl-1,2-diaryl-1,2-dihydro-5-methyl-3H-pyrazol-3-onen5 wird beschrieben. Die Reaktion von 4,4-disubstituierten 1,2-Diaryl-hydrazinen1 mit Essigsäureanhydrid führt in Gegenwart eines Äquivalentes 4-(Dimethylamino)pyridin zu Gemischen der entsprechenden Acetylderivate2 und3. Unter den gleichen Bedingungen werden aus 2,2-disubstituierten 1,2-Diarylhydrazinen Gemische aus3 und5 erhalten.相似文献
65.
Jaroslav Kalvoda Jüren Grob Mira Bjelakoví Ljubinka Lorenc Mihailo Lj. Mihailoví 《Helvetica chimica acta》1997,80(4):1221-1228
The two structurally similar 20-phenyl- and 20-(4-methoxyphenyl)-11-(nitrosooxy)pregnan-20-ol derivatives 4 and 7 behave differently under photolytic conditions, the former nitrous acid ester affording, as a main product, the benzo-fused hexacyclic compound 9 , and the latter the 21 -nitro derivative 12. Mechanistic aspects of these transformations are discussed. 相似文献
66.
Homologous recombination (HR) repair deficiency impairs the proper maintenance of genomic stability, thus rendering cancer cells vulnerable to loss or inhibition of DNA repair proteins, such as poly(ADP-ribose) polymerase-1 (PARP-1). Inhibitors of nuclear PARPs are effective therapeutics for a number of different types of cancers. Here we review key concepts and current progress on the therapeutic use of PARP inhibitors (PARPi). PARPi selectively induce synthetic lethality in cancer cells with homologous recombination deficiencies (HRDs), the most notable being cancer cells harboring mutations in the BRCA1 and BRCA2 genes. Recent clinical evidence, however, shows that PARPi can be effective as cancer therapeutics regardless of BRCA1/2 or HRD status, suggesting that a broader population of patients might benefit from PARPi therapy. Currently, four PARPi have been approved by the Food and Drug Administration (FDA) for the treatment of advanced ovarian and breast cancer with deleterious BRCA mutations. Although PARPi have been shown to improve progression-free survival, cancer cells inevitably develop resistance, which poses a significant obstacle to the prolonged use of PARP inhibitors. For example, somatic BRCA1/2 reversion mutations are often identified in patients with BRCA1/2-mutated cancers after treatment with platinum-based therapy, causing restoration of HR capacity and thus conferring PARPi resistance. Accordingly, PARPi have been studied in combination with other targeted therapies to overcome PARPi resistance, enhance PARPi efficacy, and sensitize tumors to PARP inhibition. Moreover, multiple clinical trials are now actively underway to evaluate novel combinations of PARPi with other anticancer therapies for the treatment of PARPi-resistant cancer. In this review, we highlight the mechanisms of action of PARP inhibitors with or without BRCA1/2 defects and provide an overview of the ongoing clinical trials of PARPi. We also review the current progress on PARPi-based combination strategies and PARP inhibitor resistance.Subject terms: Cancer therapy, Mechanisms of disease, PolyADP-ribosylation 相似文献
67.
Dr. Christiane Stoll Prof. Dr. Mihail Atanasov Jascha Bandemehr Prof. Dr. Frank Neese Clemens Pietzonka Prof. Dr. Florian Kraus Prof. Dr. Antti J. Karttunen Dr. Markus Seibald Assoc. Prof. Dr. Gunter Heymann Prof. Dr. Hubert Huppertz 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(38):9801-9813
As a consequence of the static Jahn-Teller effect of the 5E ground state of MnIII in cubic structures with octahedral parent geometries, their octahedral coordination spheres become distorted. In the case of six fluorido ligands, [MnF6]3− anions with two longer and four shorter Mn−F bonds making elongated octahedra are usually observed. Herein, we report the synthesis of the compound K3[MnF6] through a high-temperature approach and its crystallization by a high-pressure/high-temperature route. The main structural motifs are two quasi-isolated, octahedron-like [MnF6]3− anions of quite different nature compared to that met in ideal octahedral MnIII Jahn-Teller systems. Owing to the internal electric field of Ci symmetry dominated by the next-neighbour K+ ions acting on the MnIII sites, both sites, the pseudo-rhombic (site 1) and the pseudo-tetragonally elongated (site 2) [MnF6]3− anions are present in K3[MnF6]. The compound was characterized by single-crystal and powder X-ray diffraction, and magnetometry as well as by FTIR, Raman, and ligand field spectroscopy. A theoretical interpretation of the electronic structure and molecular geometry of the two Mn sites in the lattice is given by using a vibronic coupling model with parameters adjusted from multireference ab-initio cluster calculations. 相似文献
68.
Martin Möbs Prof. David A. Dixon Dr. Gabriel F. de Melo Dr. Monica Vasiliu Tim Graubner Prof. Karl O. Christe Prof. Florian Kraus 《Angewandte Chemie (International ed. in English)》2023,62(39):e202307218
The purely chemical synthesis of fluorine is a spectacular reaction which for more than a century had been believed to be impossible. In 1986, it was finally experimentally achieved, but since then this important reaction has not been further studied and its detailed mechanism had been a mystery. The known thermal stability of MnF4 casts serious doubts on the originally proposed hypothesis that MnF4 is thermodynamically unstable and decomposes spontaneously to a lower manganese fluoride and F2. This apparent discrepancy has now been resolved experimentally and by electronic structure calculations. It is shown that the reductive elimination of F2 requires a large excess of SbF5 and occurs in the last reaction step when in the intermediate [SbF6][MnF2][Sb2F11] the addition of one more SbF5 molecule to the [SbF6]− anion generates a second tridentate [Sb2F11]− anion. The two tridentate [Sb2F11]− anions then provide six fluorine bridges to the Mn atom thereby facilitating the reductive elimination of the two fluorine ligands as F2. 相似文献
69.
70.
Laser drilling of stainless steel with nanosecond double-pulse 总被引:1,自引:0,他引:1
X.D. Wang A. Michalowski D. Walter S. Sommer M. Kraus J.S. Liu F. Dausinger 《Optics & Laser Technology》2009,41(2):148-153
Nanosecond double-pulse laser drilling is reported in this paper. The double-pulse herein represents two closely conjoint pulses with 21 ns pulse duration and about 52 ns interpulse separation, which are acquired by temporal pulse shaping. Percussion drilling with such double-pulse is performed in stainless steel samples with different laser fluences, sample's thickness, repetition rates and ambient pressures. The experimental results show that the drilling rates of double-pulse drilling are more than one order of magnitude higher than that of conventional single-pulse drilling in air. Differences in the processing results between single-pulse and double-pulse with various processing parameters are investigated. In addition the ablation mechanisms of the double-pulse drilling are discussed. 相似文献