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211.
Santer S Kopyshev A Donges J Rühe J Jiang X Zhao B Müller M 《Langmuir : the ACS journal of surfaces and colloids》2007,23(1):279-285
The correlation between the morphology of mixed polymer brushes and fluctuations of the grafting points is investigated by single-chain-in-mean-field simulations and experiments. The local topography of two types of mixed polystyrene-polymethylmethacrylate (PS-PMMA) brushes that differ in their modes of attachment has been studied during repeated microphase separation into laterally structured and homogeneous morphologies upon changing solvents. In the first type of brush (conventional), each of the surface-attached initiator groups starts the growth of either a PS or a PMMA chain in a random fashion. In the second case (Y-shaped mixed brushes), two chains of different types are attached to the same anchor group on the substrate. Whereas in the first case statistical fluctuations of the chemical composition occur on a local scale, such composition fluctuations are strongly suppressed in the latter case. The microphase-separated morphology is similar in both cases, but Y-shaped brushes exhibit a significantly weaker domain memory than do conventional PS-PMMA mixed brushes. The results of the experiment are compared with simulations, and a simple phenomenological argument and qualitative agreement are found. The observations demonstrate that small fluctuations in the grafting points are amplified by the microphase separation and nucleate the location of the domains in the mixed brush. 相似文献
212.
Muravyova EA Desenko SM Musatov VI Knyazeva IV Shishkina SV Shishkin OV Chebanov VA 《Journal of combinatorial chemistry》2007,9(5):797-803
Multicomponent reactions and organic synthesis with ultrasonic activation have been used as key methods for the synthesis of tetrahydropyrimidine derivatives. The three-component condensation of 1,3-diarylprop-2-en-1-one with ammonia and aldehydes/acetone or N-substituted gamma-pyridones under ultrasonic irradiation was developed as a rapid and efficient solution-phase method for the high-yielding preparation of 2-aryl(hetaryl)-4,6-diaryl-1,2,5,6-tetrahydropyrimidines and 2,4-diaryl-1,5,9-triazaspiro[5.5]undec-1-enes. The described synthetic protocol provides rapid access to novel and diversely substituted tetrahydropyrimidines libraries. The simple, primary biological screening showed 98% of inhibitory activity against Mycobacterium tuberculosis for one of tetrahydropyrimidines synthesized. 相似文献
213.
Manner for Instantenious Determination of Base Impurity and Dissociation Constant of Carboxylic Acid
It is known that the commercial solvents are polluted of basic impurities as usual. 相似文献
214.
Svetlana I. Pomogailo Gulzhian I. Dzhardimalieva Viktoria A. Ershova Sergei M. Aldoshin Anatolii D. Pomogailo 《Macromolecular Symposia》2002,186(1):155-160
Cluster metal-containing monomers were obtained and characterized. Mono- and disubstituted products were obtained under mild conditions via the interaction of Rh6(CO)16 with 4-vinylpyridine (4-VPy) in the presence of trimethylamin-N-oxide. Substitution of labile acetonitrile ligand in Rh6(CO)15NCMe by allyldiphenylphosphine (AlPPh2) yields Rh6(CO)14(μ,η2-PPh2CH2CH=CH2) with formation of π-complex. The structures of Rh6(CO)15(4-VPy), Rh6(CO)14(μ,η2-PPh2CH2CH=CH2) and (μ-H)Os3(μ-OCNM2)(CO)9PPH2CH2CH=CH2 have been determined by single-crystal X-ray diffraction studies, as well as by IR-, 1H NMR spectroscopies. The Rh - Rh bond lengths are within 2.72÷2.80 Å. The copolymerization of cluster-containing monomers synthesized with traditional monomers has been studied. It was found that Rh6- and Os3-containing monomers did not change either the ligand surroundings or the structure of cluster monomer framework during polymerization reaction. 相似文献
215.
Sergei P. Ivonin Svetlana D. Kopteva Viktor N. Serdyuk Andrei A. Tolmachev Aleksandr M. Pinchuk 《Heteroatom Chemistry》2001,12(7):652-657
This study covers phosphorylation of heterocyclic analogues of N‐methyldiphenylamine with phosphorus tribromide in pyridine solution. The reaction is found to proceed regioselectively in accordance with the orienting effect of the amino group. Mono and bis‐phosphorylated derivatives of the heterocycles have been isolated and characterized. It is pointed out that the heterocyclic systems under study exhibit reduced reactivity in electrophilic phosphorylation as compared to N‐methyldiphenylamine. The results of calculations by the PM3 method are reported for the starting molecules and their σ‐complexes. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:652–657, 2001 相似文献
216.
Irina YU. Gorbunova Michail L. Kerber Svetlana I. Vladimirova Reem R. Musleh Nickolay N. Avdeev 《Macromolecular Symposia》1998,127(1):187-192
Miscibility of polypropylene with some oligoesters was evaluated by optical wedge interference microscopy. Mechanical, thermal, rheological and relaxation properties were studied. Compatibility between the polymers and modifying agents was shown to have a marked effect on stress-strain properties as well as on the structure and melting characteristics of the modified polymers. 相似文献
217.
Kalina Kostova Vladimir Dimitrov Svetlana Simova Manfred Hesse 《Helvetica chimica acta》1999,82(9):1385-1399
The allylic and homoallylic alcohols 1 – 8 , prepared from (+)-camphor and (−)-fenchone, were ozonized in Et2O at −78° and treated with Et3N or LiAlH4 to give the chiral hydroxy carbonyl compounds 9 – 16 and the diols 17 – 24 , respectively (Scheme 1). In the case of the diols 19 and 24 , the formation of new chiral centers proceeded with high diastereoselectivity. These diols were prepared highly diastereoselectively also by LiAlH4 reduction of the hydroxy carbonyl compounds 11 and 16a , respectively (Scheme 2). The absolute configuration of the new chiral centers in 19 and 24 was determined by X-ray and NMR methods. The ozonization of compounds 2 , 3 , 7 , and 8 provided the relatively stable hydroxy-substituted 1,2,4-trioxolane derivatives (ozonides) 37 – 40 (Scheme 5) which were characterized by 1H- and 13C-NMR spectra, ESI-MS, and natural-abundance 17O-NMR spectra. 相似文献
218.
Sergey P. Gromov Svetlana N. Dmitrieva Artem I. Vedernikov Nikolay A. Kurchavov Lyudmila G. Kuz'mina Yuri A. Strelenko Michael V. Alfimov Judith A. K. Howard 《Journal of Physical Organic Chemistry》2009,22(9):823-833
An improved method for the synthesis of formyl derivatives of N‐methylbenzoazacrown ethers is proposed. They are prepared in up to 68% yields over fewer steps and with a much shorter time required for the last step. The stability constants of complexes formed by N‐methylbenzoazacrown ethers and their structural analogs with alkali metal, alkaline‐earth metal and ammonium cations were determined by 1H NMR titration in CD3CN. High stability of complexes of N‐methyl derivatives of benzoazacrown ethers is demonstrated, comparable with or even exceeding the stability of benzocrown‐ether complexes and markedly exceeding the stability of complexes of phenylazacrown ethers with the same macrocycle size. The structures of azacrown ethers and their complexes with Ba(ClO4)2 were studied by X‐ray diffraction. A high degree of pre‐organization of N‐methylbenzoazacrown ethers toward the formation of complexes with metal and ammonium cations was noted, which is due to the clear‐cut pyramidal geometry of the nitrogen atom and the orientation of the lone electron pairs (LEPs) of most heteroatoms towards the centre of the macroheterocycle. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
219.
Michael Ph. Pyshnyi Svetlana V. Pyshnaya Galina S. Nechitailo Anatoly A. Kuznetsov 《Journal of magnetism and magnetic materials》2009,321(10):1552-1556
We considered applicability of acoustic imaging technology for the detection of magnetic microparticles and nanoparticles inside soft biological tissues. Such particles are widely used for magnetically targeted drug delivery and magnetic hyperthermia. We developed a new method of ultrasonic synchronous tissue Doppler imaging with magnetic modulation for in vitro and in vivo detection and visualization of magnetic ultradisperse objects in soft tissues. Prototype hardware with appropriate software was produced and the method was successfully tested on magnetic microparticles injected into an excised pig liver. 相似文献
220.
Vijay Singh R.P.S. Chakradhar Isabelle Ledoux-Rak Laurent Badie Fabienne Pelle Svetlana Ivanova 《Journal of luminescence》2009,129(11):1375-1380
New near-infrared luminescent, monoclinic CaAl2O4:Er3+ phosphor was prepared by using the combustion route at furnace temperatures as low as 500 °C in a few minutes. Combustion synthesized phosphor has been well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive analysis of X-ray (EDAX) mapping studies. The luminescence spectra of Er3+-doped calcium aluminate were studied at UV (380 nm), vis (488 nm) and IR (980 nm) excitation. Upon UV and vis excitation, the CaAl2O4:Er3+ phosphor exhibits emission bands at ~523 nm and at ~547 nm, corresponding to transitions from the 2H11/2 and 4S3/2 erbium levels to the 4I15/2 ground state. A strong luminescence at 1.55 μm in the infrared (IR) region due to 4I13/2→4I15/2 transition has been observed in CaAl2O4:Er3+ phosphor upon 980 nm CW pumping. In the spectrum of IR-excited up-conversion luminescence, green (~523 and ~547 nm) and red (662 nm) luminescence bands were present, the latter associated with the 4F9/2→4I15/2 transitions of Er3+ ions. Both excited state absorption and energy transfer may be proposed as processes responsible for the population of the 4S3/2 and 4F9/2 erbium levels upon IR excitation. The mechanisms responsible for the up-conversion luminescence are discussed. 相似文献