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2.
Parabolic Capacity and Soft Measures for Nonlinear Equations   总被引:2,自引:0,他引:2  
We first introduce, using a functional approach, the notion of capacity related to the parabolic p-Laplace operator. Then we prove a decomposition theorem for measures (in space and time) that do not charge the sets of null capacity. We apply this result to prove existence and uniqueness of renormalized solutions for nonlinear parabolic initial boundary-value problems with such measures as right-hand side.  相似文献   
3.
Bubbles released from a porous plug into a gas-stirred ladle present different bubbly dispersion patterns that can be studied by CFD means. Recent modeling (Alexiadis et al.) has, in fact, led to numerical results in accord with experimental data. However, due to the high number of equations involved, it is not easy to understand the physical reasons of the transitions between these patterns. In the present paper, attention was focused on the role of fragmentation and coalescence and the pattern-transition modeled by means of intersection points between these functions.  相似文献   
4.
Summary A statistical study of precipitation over the Po Valley and the Alps during four winters, based on the application of a principal component (p.c.) method, exhibited a good correlation between the first three rotated eigenvectors of the cross-product matrix (between time series of data recorded at 70 stations) and three typical atmospheric circulation schemes over Northern Italy. The study is here continued, by relating these results to meteorological fields evaluated over a region wider than the area previously considered. Our attention mainly concentrated on the fields of time trend of geopotential height at 850 hPa over Europe, between latitude 34.5 and 51 degrees North and longitudes 0 and 21 degrees East. This was suggested by some peculiar relationships shown by the statistical distributions of geopotential height and wind direction and speed with respect to the first three p.c.’s. These relationships made us think of the possibility to use those trends as predictors of precipitation fields. Our analysis puts into evidence that three spatial patterns of geopotential, height time trend can be safely associated to the first three p.c.’s and, as a consequence, to the three precipitation modes corresponding to the spatial distributions of the eigenvectors, previously identified by us. They can therefore be considered meaningful precursors of precipitation field patterns over Northern Italy and Alpine regions.
Riassunto Uno studio statistico della precipitazione sulla pianura padana e sulle Alpi durante quattro inverni, basato sull’applicazione del metodo delle componenti principali (c.p.), ha mostrato una buona correlazione fra i primi tre autovettori rotati della matrice dei prodotti incrociati (fra le serie temporali dei dati registrati in 70 stazioni) e tre tipici schemi di circolazione atmosferica sull’Italia del Nord. Lo studio viene qui prosequito, mettendo in relazione tali risultati con campi meteorologici valutati su una zona piú ampia di quella precedentemente considerata. La nostra attenzione si è prevalentemente concentrata sui campi di tendenza temporale dell’altezza di geopotenziale a 850 hPa sull’Europa, a latitudini comprese tra 34.5 e 51 gradi Nord e longitudini fra 0 e 21 gradi Est. Ciò è stato suggerito da alcune relazioni peculiari mostrate dalle distribuzioni statistiche di altezza di geopotenziale e di direzione ed intensità del vento rispetto alle prime tre c.p., che ci hanno fatto pensare alla possibilità di usare tali tendenze come predittori del campo di precipitazione. La nostra analisi ha messo in evidenza il fatto che tre distribuzioni spaziali di tendenza temporale del campo di altezza di geopotenziale possono essere con sicurezza associate alle prime tre c.p. e., quindi, ai tre modi di precipitazione corrispondenti alle distribuzioni spaziali degli autovettori precedentemente da noi identificati. Essi possono pertanto essere considerati significativi precursori del campo di precipitazione sull’Italia del Nord e sulle regioni alpine.

Резюме Статистическое исследование выпадения осадков над долиной реки По и Альпами в течение четырех зим, основанное на применении метода главных компонент, обнаруживает хорошую корреляцию между первыми тремя вращающимися собственными векторами матрицы векторного произведения (между временными последовательностями данных, зарегистрированных на 70 станциях) и тремя схемами типичной атмосферной циркуляции над Северной Италией. В этой работе продолжены исследования. Полученные результаты связывайотся с метеорологическими полями, вычисленными над областью, которая шире ранее рассмотренной области. Главное внимание мы обращаем на поля временного хода для геопотенциальной высоты при 850гПа над Европой, между 34.5щ и 51щ северной широты и между 0щ и 21щ восточной долготы. Это следует из специальных соотношений, полученных с помощью статистических распределений геопотенциальной высоты и направления и скорости ветра относительно первых трех главных компонент. Эти соотношения позволяют нам использовать исследованные тенденции, как предсказатели полей вьшадения осадков. Нам анализ подтверждает, что три пространственным распределения временного хода для геопотенциальной высоты могут быть связаны с первыми тремя главными компонентами и, как следствие, с тремя моделями выцадения осадков, которые соответствуют пространственным распределениям собственных векторов, ранее идентифицированных в работе [Ш]. Следовательно, они могут рассматриватяся как предвестники для распределений полей осадков над Северной Италией и над Альпами.
  相似文献   
5.
Alessio Porta 《Tetrahedron》2007,63(19):3989-3994
A highly enantioselective synthesis of the (8S,12S)-enantiomer of preclavulone A and its methyl ester is described featuring the Julia protocol for installing the (Z)-double bond in the lower chain. This procedure is suitable for the preparation of labeled preclavulone analogues for biosynthetic studies on marine clavulones.  相似文献   
6.
Summary Complete Active-Space Self-Consistent-Field (CAS-SCF) calculations for cubic N8 are presented. We studied the N8↔4N2 reaction inD 4h symmetry and found its energy release and activation barrier with three different atomic basis sets. The energy release for this reaction is predicted to be around 526 kcal/mol, while the energy barrier to dissociation is estimated about 159 kcal/mol. These results are in substantial agreement with previousab initio estimates. The authors of this paper have agreed to not receive the proofs for correction.  相似文献   
7.
A method based on ior-pair reversed-phase liquid chromatography is reported for the determination of climbazol, a preservative used in cosmetic products. The column was packed wit LiChrosob RP-18, the mobile phase was acetonitrile-sodium perchlorate (0.05 M, pH 3.0) (40 + 60) and detection was at 224 nm. The method was applied to the analysis of commercial shampoos. The detection limit was 10 ng injected and calibration linearity was observed up to 6 μg.  相似文献   
8.
Specific programming of automated HPLC systems allows total on-line qualification, validation and stability monitoring using the concept of deferred standards. Setting up such a process for routine analyses in an automated HPLC system requires specific autosampler programming as well as specific monitoring software. With an autosampler, a double injection procedure is programmed, the first introducing the sample, and the second, a few minutes deferred, the deferred control standard. Two additional compounds are therefore added to the sample before and during the chromatographic process: the intemal standard for sample quantification and the deferred standard for system control. Specific methodologies are described of how to obtain classical quantitative analysis information as well as system qualification validation stability information. Experiments were performed to develop specified methodologies to monitor the quality of quantitative analysis during the life of the column by using the deferred standard concept to probe the effects of column ageing on separation characteristics.  相似文献   
9.
Regioconvergent synthesis of the key lactone 1 from an equimolar mixture of the two olefins 4 and 5 was achieved by unique Pd(II) chemistry. The synthetic versatility of lactone 1 has been demonstrated in the synthesis of iridoids and of the endo-Corey lactone 2, which is a key intermediate for the F(2)-isoprostane synthesis. Upon exposure of the sodium salts of 4 and 5 to a catalytic amount of Pd(OAc)(2) under oxygen, in the presence of AcOH, an isomeric lactone 12 was obtained in addition to the title compound 1. The Pd(II) lactonization was optimized by fine-tuning all the factors participating in the catalytic cycle: solvent, oxidant, co-oxidant, and Pd(II) source. The Hosokawa's heterobimetallic couple emerged as the catalyst of choice. With a Cu(II)-Pd(II) couple, the redox process was transferred to copper, and the formal oxidation state of palladium remained constant during the reaction. By virtue of this new methodology, lactone 1 was obtained in a rewarding 60% yield, along with isomeric lactone 12 in 30% yield. A detailed mechanistic study was carried out in order to elucidate the formation of lactones 1 and 12. Lactone 1 was formed from either olefin 8 or olefin 10; on the other hand, lactone 12 was formed exclusively from olefin 10. An intramolecular 1,2-acyloxypalladiation was invoked for the transformation of 8 into 1, whereas the pi-allyl complexes 13 and 11 were involved in the transformation of olefin 10 into 12 and 1, respectively.  相似文献   
10.
Zusammenfassung Zwei Methoden zur extraktiven Abtrennung des Urans von einer Reihe von Ionen werden beschrieben. Die Extraktion erfolgt aus schwefelsaurer Lösung mit N-Benzylanilin bzw. N-Butylanilin, gelöst in Chloroform. Nach Reextraktion mit Wasser erfolgt die quantitative Bestimmung mit PAR.
Summary Two methods for the extractive separation of uranium from a number of ions are described. The extraction is from a solution containing sulfuric acid by means of N-benzylaniline or N-butylanilin, dissolved in chloroform. After reextraction with water, there follows the quantitative determination with PAR.
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