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141.
Khazaei M Liang Y Bahramy MS Pichierri F Esfarjani K Kawazoe Y 《J Phys Condens Matter》2011,23(40):405403
We have performed a set of first-principles simulations to consider the possible phase transitions in molecular crystals of HCN under high pressure. Our calculations reveal several transition paths from the orthorhombic phase to tetragonal and then to triclinic phases. The transitions from the orthorhombic to the tetragonal phases are of the second order, whereas those from the tetragonal to the triclinic phases turn out to be of the first-order type and characterized by an abrupt decrease in volume. Our calculations show that, by adjustment of the temperature and pressure of the HCN molecular crystal, novel layered and polymeric crystals with insulating, semiconducting or metallic properties can be found. Based on our simulation results, two different crystal formation mechanisms are deduced. The stabilities of the predicted structures at ambient pressure are further assessed by performing phonon or MD simulations. In addition, the electron transport properties of the predicted polymers are obtained using the non-equilibrium Green's function technique combined with density functional theory. The results show that the polymers have metallic-like I-V characteristics. 相似文献
142.
Yaghoub Haghighatnia Saeed Balalaie Hamid Reza Bijanzadeh 《Helvetica chimica acta》2012,95(5):818-824
Some new amidated fentanyl (=N‐[1‐(2‐phenylethyl)piperidin‐4‐yl]‐N‐phenylpropanamide) analogs with a 4‐(N‐phenylamido)piperidine scaffold and additional amide bonds have been designed and synthesized through Ugi four‐component reaction (Ugi‐4CR). Good‐to‐high yields, diversity‐oriented synthesis, and possible applications in drug discovery are advantages of this approach. 相似文献
143.
We prove that the only possible biaccessible points in the Julia set of a Cremer quadratic polynomial are the Cremer fixed point and its preimages. This gives a partial answer to a question posed by C. McMullen on whether such a Julia set can contain any biaccessible point at all.
144.
Summary This paper describes the application of capillary electrochromatography (CEC) to the rapid quantitative analysis of individual
mono- and dihydroxy phenols in tobacco smoke. The method derived provides reproducible and quantitative analysis of real samples,
in significantly shorter times than are achieved by current GC and HPLC methods. 相似文献
145.
Saeed Farrokhpay 《应用光谱学评论》2013,48(3):233-243
Abstract: This article presents a review of the published articles related to the novel application of spectroscopy and microscopy methods in paint and coatings quality evaluation. Traditional and simple techniques have been used in paint and coating industry for many years and proven to be effective. However, the paint and coating industry faces new formulations with nontraditional applications. Therefore, the industry needs to adjust itself with the current sophisticated production and testing methods. There are a number of modern microscopy and spectroscopy techniques that can be utilized in the paint and coating industry for a better understanding of the product quality and/or application performance. This, in particular, is highly applicable in modern and nontraditional applications such as nanotechnology and smart coatings. Though importance of spectroscopy and microscopy methods is being increasingly recognized in the industry, there is no current comprehensive review available to highlight the need for novel application of these techniques in surface coatings evaluations. 相似文献
146.
Morteza BararjanianSaeedeh Hosseinzadeh Saeed Balalaie Hamid Reza BijanzadehEckardt Wolf 《Tetrahedron letters》2011,52(26):3329-3332
An efficient palladium-catalyzed protocol for the stereoselective synthesis of 3-(aminoarylmethylene)-oxindoles has been developed. In this approach, Ugi-4-component reaction adducts were used as starting materials for carbopalladative cyclization-Buchwald reaction sequences. 相似文献
147.
G. Morel O. Samhan P. Literathy H. Al-Hashash L. Moulin T. Saeed K. Al-Matrouk M. Martin-Bouyer A. Saber L. Paturel J. Jarosz M. Vial E. Combet C. Fachinger J. Suptil 《Fresenius' Journal of Analytical Chemistry》1991,339(10):699-715
Summary Analytical protocols have been adapted for the study of hydrocarbons at the trace level in the environment. Various samples, including sediments and biota, were collected from the Kuwaiti environment, treated according to the protocol and analyzed by chromatographic and spectroscopic methods. The methods used were synchronous scanning fluorescence spectroscopy (SSFS); high-performance liquid chromatography (HPLC) on C18 reversed-phase and NH2 normal-phase columns with UV and fluorescence detectors; gas chromatography on fused-silica capillary columns (GC) with flame ionization detector (FID), mass spectrometer (MS) and flame photometric detector (FPD); and high-resolution molecular spectrofluorimetry in Shpol'skii matrix at 10 K (HRSS). The different methods were found to give complementary information. SSFS was useful for fast evaluation and preliminary assessment of oil pollution during extended programs; it permitted sample selection for deeper analyses but, when applied to biota, needed special care in the clean-up procedure. GC/FID, was used to analyze saturated and ethylenic compounds and was useful for obtaining information on the origin of hydrocarbons but inconvenient for analyzing the aromatic fraction. GC/FPD was difficult to use with sediment samples and yielded little information on biota samples, although it did permit confirmation of high oil contamination in some examples. HPLC on a normal-phase column with UV and fluorescence detectors was useful for the fractionation of samples and for the separation of different families of aromatic compounds according to aromatic carbon number. GC/MS was used to quantify polycyclic aromatic hydrocarbons (PAHs) of less than four cycles but was not sensitive enough for PAHs of higher molecular weight. HRSS, however, was useful for the quantification of heavy PAHs and was also faster, could be automated, and gave accurate results. However, in an oil-pollution study, it must be backed up by the other techniques. In fact, no single analytical technique was found to be sufficient, and only judicious combinations of the tested techniques yielded adequate information on the origin of hydrocarbons in the environment. 相似文献
148.
Irfan Saeed Fareha Zafar Khan Masashi Shiotsuki Toshio Masuda 《Journal of polymer science. Part A, Polymer chemistry》2009,47(7):1853-1863
The 3‐ and 4‐aminophenylacetylenes protected by t‐butoxycarbonyl (t‐Boc) and 9‐fluorenylmethoxycarbonyl (Fmoc) groups ( 3a – 6a ) were synthesized and polymerized using [(nbd)RhCl]2 ( 1 ) and [(nbd)Rh+‐η6‐PhB?Ph3] ( 2 ) catalysts. The t‐Boc‐containing polymers [poly( 3a ) and poly( 4a )] were obtained in high yield (82–91%). Among the Fmoc‐protected monomers, the para‐derivative polymerized well [poly( 6a ); yield = 85–94%], whereas its meta‐substituted analogue did not afford high molecular weight polymer in good yield [poly( 5a ); yield = 10–15%]. The use of KN(SiMe3)2 as a cocatalyst in conjunction with 1 led to a dramatic increase in the molecular weight of the polymers. The acid‐ and base‐catalyzed removal of the t‐Boc and the Fmoc groups, respectively, generated primary amine‐containing polymers [poly( 3b )–poly( 6b )] which cannot be obtained directly by the polymerization of the corresponding monomers. The solubility characteristics of the polymers bearing protected amino groups were quite different from those of the unprotected ones, the former being soluble in polar solvents, whereas the latter displayed poor solubility even in polar protic or highly polar aprotic solvents. The attempts to accomplish the free‐standing membrane fabrication by solution casting were successful only for poly( 3a ), and an augmentation in the gas permeability and CO2/N2 permselectivity was discerned in comparison with the unsubstituted poly(phenylacetylene) and poly(m‐t‐butyldimethylsiloxyphenylacetylene). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1853–1863, 2009 相似文献
149.
Reza Zadmard Dr. Saeed Taghvaei‐Ganjali Dr. Banafsheh Gorji Dr. Thomas Schrader Prof. Dr. 《化学:亚洲杂志》2009,4(9):1458-1464
A dimeric calixarene, with an aliphatic C6‐bridge and six anilinium head groups at its upper rim, preferably complexes diphosphates and oligonucleotides with more than 10 bonds between both anionic moieties. Free binding energies correlate with the length of the aliphatic bridge in a roughly linear fashion. The binding event, which is monitored by fluorescence titrations and competition experiments, relies on Coulomb interactions, as opposed to a nonpolar variant with tert‐butyl instead of ammonium groups; here, hydrophobic forces prevail, rendering the calixarene dimer selective for less polar cofactors such as FAD. The best guest for the hexaanilinium dimer is found in ssDNA, which carries multiple copies of the optimal trinucleotide for maximum attraction towards the extended cationic host. The recognition event is also observed in the environment of a lipid monolayer, and provides a means to quantify dimer diphosphate interactions by measuring p/A shifts. 相似文献
150.