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91.
Balaban MC Eichhöfer A Buth G Hauschild R Szmytkowski J Kalt H Balaban TS 《The journal of physical chemistry. B》2008,112(17):5512-5521
The title dicyano compound was synthesized via cyanation and it self-assembles in nonpolar solvents giving red-shifted and broad absorption maxima just as the bacteriochlorophylls which are encountered in the light-harvesting organelles of early photosynthetic bacteria. In the crystal, stacks are formed through a hierarchic combination of pi-stacking and a CN-Zn electrostatic interaction. Push-pull 15-N,N-dialkylamino-5-cyano congeners could be obtained in high yields using a solvent- and catalyst-free direct amination of meso-bromoporphyrins. Importantly, the fluorescence of the self-assembled species due to the very orderly manner in which the chromophores are arranged is not entirely quenched and has a surprisingly long lifetime of over 1 ns. This lends hope of using the trapped energy in biomimetic hybrid solar cells. 相似文献
92.
Laura Mureşan Ruben Ronda Valera Ivo Frébort Ionel Catalin Popescu Elisabeth Csöregi Mihaela Nistor 《Mikrochimica acta》2008,163(3-4):219-225
A selective and sensitive method is presented for biogenic amines (BA) determination. The novelty consists in coupling a highly selective electrochemical biosensor to a weak acid cation-exchange column for online detection of amines. A bienzyme design, based on a recently isolated amine oxidase from grass pea and commercial horseradish peroxidase, was used for the biosensor construction. The enzymes were co-immobilized on the surface of a graphite electrode together with the electrochemical mediator (Os-redox polymer). The electrochemical detection was performed at a low applied potential (?50 mV vs. Ag/AgCl, KCl0.1 M), where biases from interferences are minimal. The separation and determination of six BA, with relevance in food analysis (tyramine, putrescine, cadaverine, histamine, agmatine and spermidine), were investigated. Irrespective of the BA nature, the amine oxidase-based biosensor showed a linear response up to 5 mM, and its sensitivity decreases in the following order: cadaverine, putrescine, spermidine, agmatine, histamine and tyramine. The approach was used to estimate the BA content in fish samples, after their extraction with methanesulfonic acid. 相似文献
93.
Validation of the Tessier scheme for speciation of metals in soil using the Bland and Altman test 总被引:1,自引:0,他引:1
Tiberiu Frentiu Michaela Ponta Erika Levei Emilia Gheorghiu Iosif Kasler Emil A. Cordos 《Chemical Papers》2008,62(1):114-122
The Tessier extraction method was used for speciation of Cu, Pb, Zn, As, Fe and Mn in a large concentration range in contaminated
soil with various mineralogical compositions. The results were compared by X-ray fluorescence spectrometry (XRF) as a reference
method using the Bland and Altman test. A sum of five fractions (exchangeable, bound to carbonates, Fe-Mn oxides, organic
matter and residual forms) was compared with the total content determined on solid matrix by the reference method. A good
agreement between the methods in the whole concentration range was found for Cu, Zn, As, and Fe. For Mn and Pb, XRF was found
suitable to verify the sequential extraction only for concentrations above 250 mg kg−1. This was a consequence of a poorer reproducibility of Pb extraction using the Tessier scheme due to a great difference in
the mineralogical composition and the diversity of the Pb species identified in soil. The poorer result of Mn was attributed
to the spectral interference of Fe in XRF.
Presented at the 34th International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 21–25 May
2007. 相似文献
94.
95.
Caprioara M Fiammengo R Engeser M Jäschke A 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(7):2089-2095
In order to expand the repertoire of DNA sequences specifically interacting with transition metals, we report here the first examples of DNA sequences carrying mono- and bidentate phosphane ligands as well as P,N-ligands. Aminoalkyl-modified oligonucleotides have been reacted at predetermined internal sites with carboxylate derivatives of pyrphos, BINAP and phosphinooxazoline (PHOX) 2 b-d. Carbodiimide coupling in the presence of N-hydroxysuccinimide provided the DNA-ligand conjugates in 38-78 % yield. Phosphane-containing oligonucleotides and their phosphane sulfide analogues were characterized by mass spectrometry (MALDI-TOF and FT-ICR-ESI) and their stability after purification and isolation was systematically investigated. While DNA-appended pyrphos ligand was quickly oxidized, BINAP and PHOX conjugates showed high stabilities, making them useful precursors for incorporation of transition metals into DNA. 相似文献
96.
97.
Linda Leme Mihaela Gulea Monique Saquet Serge Masson Noël Collignon 《Heteroatom Chemistry》1999,10(4):281-289
New variously substituted 1‐dimethylamino or 1‐methylthio but‐3‐enylidene‐bis‐phosphonates have been prepared from readily availableα‐dimethylamino or α‐methylthio methylene‐bis‐phosphonates by postulated [2,3]‐Wittig rearrangements of the corresponding N‐ or S‐allylic intermediate ylides. © 1999 John Wiley & Sons, Inc. Heteroatom Chem 10: 281–289, 1999 相似文献
98.
Mihaela Ginj 《Tetrahedron letters》2005,46(16):2821-2824
It is now well established that the biological effects of Auger-emitting radionuclides are critically dependent on their subcellular location. Therefore, for their use in molecular imaging and targeted radionuclide therapy, attempts should be made to increase the nuclear specificity of the carriers. In the present paper the synthesis of novel trifunctional somatostatin derivatives containing a nuclear localization motif is described. These derivatives of [DOTA0, Tyr3]-octreotide (DOTATOC, DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) were obtained in high yields using Fmoc peptide synthesis in solid and in solution phase. 相似文献
99.
Irina Ielciu Mihaela Niculae Emoke Pall Cristina Barblat Ioan Tomu Neli-Kinga Olah Ramona Flavia Burtescu Daniela Benedec Ilioara Oniga Daniela Hanganu 《Molecules (Basel, Switzerland)》2022,27(13)
Rosmarinus officinalis L. is a species that is widely known for its culinary and medicinal uses. The purpose of the present study consisted of the evaluation of the antiproliferative and antimicrobial effects of R. officinalis-loaded liposomes (L-R). Characterization of the liposomes was performed by establishing specific parameters. The load of the obtained liposomes was analyzed using an LC-MS method, and antiproliferative assays evaluated the cell viability on a liver adenocarcinoma cell line and on a human hepatic stellate cell line. Antimicrobial assays were performed by agar–well diffusion and by broth microdilution assays. The obtained liposomes showed high encapsulation efficiency, suitable particle size, and good stability. High amounts of caffeic (81.07 ± 0.76), chlorogenic (14.10 ± 0.12), carnosic (20.03 ± 0.16), rosmarinic (39.81 ± 0.35), and ellagic (880.02 ± 0.14) acids were found in their composition, together with other polyphenols. Viability and apoptosis assays showed an intense effect on the cancerous cell line and a totally different pattern on the normal cells, indicating a selective toxicity towards the cancerous ones and an anti-proliferative mechanism. Antimicrobial potential was noticed against all tested bacteria, with a better efficacy towards Gram-positive species. These results further confirm the biological activities of R. officinalis leaf extract, and proposes and characterizes novel delivery systems for their encapsulation, enhancing the biological activities of polyphenols, and overcoming their limitations. 相似文献
100.
Electrochemical Behaviour and Rapid Determination of L‐Dopa at Electrochemically Pretreated Screen Printed Carbon Electrode 下载免费PDF全文
Andreea Alexandra Rabinca Mihaela Buleandra Adriana Balan Ioan Stamatin Anton Alexandru Ciucu 《Electroanalysis》2015,27(10):2275-2279
A simple and rapid voltammetric method based on a disposable electrochemically pretreated screen‐printed carbon electrode is proposed for the determination of L ‐dopa. Under optimum differential pulse voltammetry conditions a limit of detection of 3.6×10?7 M for L ‐dopa was obtained. The method was successfully applied to the determination of L ‐dopa in a commercial pharmaceutical formulation. 相似文献