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301.
László Szabó Loredana F. Leopold Bogdan I. Cozar Nicolae Leopold Krisztian Herman Vasile Chiş 《Central European Journal of Chemistry》2011,9(3):410-414
Soil contamination by metals is a common problem encountered in many industrialized countries. In this work we present a new
approach for heavy metals detection by using surface-enhanced Raman scattering (SERS) spectroscopy. Zn(II) can be clearly
determined by SERS in contaminated soil by using 4-(2-pyridylazo) resorcinol (PAR) as chelating molecule for the metal ion.
The SERS spectra of PAR, of its metal chelates and of the soil extract-PAR mixture were recorded using a hydroxylamine reduced
silver colloid. An excellent match of the PAR-contaminated soil extracts SERS spectrum to the Zn(PAR)2 SERS spectrum can be observed, demonstrating the presence of Zn(II) in the soil probes. Density functional theory (DFT) based
calculations were also performed for a reliable assignment of SERS spectra. 相似文献
302.
Procopio A Dalpozzo R De Nino A Maiuolo L Nardi M Romeo G 《Organic & biomolecular chemistry》2005,3(22):4129-4133
Er(OTf)3 is proposed as new efficient Lewis acid catalyst in a mild deprotection protocol of benzylidene derivatives. In a modified procedure, where acetic anhydride is used as the reaction solvent, the simultaneous cleavage of the benzylidene acetal and the peracetylation of the substrates is obtained in quantitative yields and very short reaction times. 相似文献
303.
Angela Kriza Mariana Loredana Dianu Cristian Andronescu Adina Elena Rogozea Adina Magdalena Musuc 《Journal of Thermal Analysis and Calorimetry》2010,100(3):929-935
New copper (II) complexes of Schiff bases with 1,2-di(imino-2-aminomethylpyridil)ethane with the general composition CuLX m (H2O) x , [L = Schiff base, X = Cl?, Br?, NO3 ?, ClO4 ?, CH3COO?, m = 2; X = SO4 2?, m = 1] were prepared by template synthesis. The complexes were characterized by elemental analysis, conductivity measurements, magnetic moments, IR, UV–VIS and EPR spectra. The thermal behavior of complexes was studied using thermogravimetry (TG), differential thermal analysis (DTA) and differential scanning calorimetry (DSC). Infrared spectra of all complexes are in good agreement with the coordination of a neutral tetradentate N4 ligand to the cooper (II) through azomethinic and pyridinic nitrogen. Magnetic, EPR and electronic spectral studies show a monomeric distorted octahedral geometry for all Cu(II) complexes. Conductance measurements suggest the non-electrolytic nature of the compounds, except for copper (II) nitrate and perchlorate complexes which are 1:2 electrolytes. Heats of decomposition, ΔH, associated with the exothermal effects were also determined. 相似文献
304.
Sampedro D Migani A Pepi A Busi E Basosi R Latterini L Elisei F Fusi S Ponticelli F Zanirato V Olivucci M 《Journal of the American Chemical Society》2004,126(30):9349-9359
Protonated Schiff bases (PSBs) of polyenals constitute a class of light-driven switchers selected by biological evolution that provide model compounds for the development of artificial light-driven molecular devices or motors. In the present paper, our primary target is to show, through combined computational and experimental studies, that it is possible to approach the design of artificial PSBs suitable for such applications. Below, we use the methods of computational photochemistry to design and characterize the prototype biomimetic molecular switchers 4-cyclopenten-2'-enylidene-3,4-dihydro-2H-pyrrolinium and its 5,5'-dimethyl derivative both containing the penta-2,4-dieniminium chromophore. To find support for the predicted behavior, we also report the photochemical reaction path of the synthetically accessible compound 4-benzylidene-3,4-dihydro-2H-pyrrolinium. We show that the preparation and photochemical characterization of this compound (together with three different N-methyl derivatives) provide both support for the predicted photoisomerization mechanism and information on its sensitivity to the molecular environment. 相似文献
305.
306.
Photoinduced Charge Separation in a Donor–Spacer–Acceptor Dyad with N‐Annulated Perylene Donor and Methylviologen Acceptor 下载免费PDF全文
Dr. Marie‐Pierre Santoni Antonio Santoro Tania M. G. Salerno Prof. Fausto Puntoriero Dr. Francesco Nastasi Dr. M. Letizia Di Pietro Dr. Maurilio Galletta Prof. Sebastiano Campagna 《Chemphyschem》2015,16(15):3147-3150
The first donor–acceptor species in which a strongly emissive N‐annulated perylene dye is connected to a methylviologen electron acceptor unit via its macrocyclic nitrogen atom, is prepared by a stepwise, modular procedure. The absorption spectra, redox behavior, spectroelectrochemistry and photophysical properties of this dyad and of its model species are investigated, also by pump–probe fs transient absorption spectroscopy. Photoinduced oxidative electron transfer from the excited state of the dyad, centered on the N‐annulated perylene subunit, to the appended methyviologen electron acceptor takes place in a few ps. The charge‐separated species recombines in 19 ps. Our results indicate that N‐annulated perylene can be connected to functional units by taking advantage of the macrocyclic nitrogen, an option never used until now, without losing their properties, so opening the way to new designing approaches. 相似文献
307.
Loredana Canfora Sebastien Pillet Enrique Espinosa Giuseppe Ruisi 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(10):o503-o507
The molecular structure of 7‐amino‐2‐methylsulfanyl‐1,2,4‐triazolo[1,5‐a]pyrimidine‐6‐carboxylic acid is reported in two crystal environments, viz. as the dimethylformamide (DMF) monosolvate, C7H7N5O2S·C3H7NO, (I), and as the monohydrate, C7H7N5O2S·H2O, (II), both at 293 (2) K. The triazolo[1,5‐a]pyrimidine molecule is of interest with respect to the possible biological activity of its coordination compounds. While the DMF solvate exhibits a layered structural arrangement through N...O hydrogen‐bonding interactions, the monohydrate displays a network of intermolecular O...O and N...O hydrogen bonds assisted by cocrystallized water molecules and weak π–π stacking interactions, leading to a different three‐dimensional supramolecular architecture. Based on results from topological analyses of the electron‐density distribution in X—H...O (X = O, N and C) regions, hydrogen‐bonding energies have been estimated from structural information only, enabling the characterization of hydrogen‐bond graph energies. 相似文献
308.
Loredana Elena Nita Alexandra Croitoriu Alexandru M. Serban Maria Bercea Alina G. Rusu Alina Ghilan Maria Butnaru Liliana Mititelu-Tartau Aurica P. Chiriac 《Macromolecular bioscience》2023,23(3):2200451
Short aromatic peptide derivatives, i.e., peptides or amino acids modified with aromatic groups, such as 9-fluorenylmethoxycarbonyl (Fmoc), can self-assemble into extracellular matrix-like hydrogels due to their nanofibrillar architecture. Among different types of amino acids, lysine (Lys) and glycine (Gly) are involved in multiple physiological processes, being key factors in the proper growth of cells, carnitine production, and collagen formation. The authors have previously successfully presented the possibility of obtaining supramolecular gels based on Fmoc-Lys-Fmoc and short peptides such as Fmoc-Gly-Gly-Gly in order to use them as a substrate for cell cultures. This paper investigates how the introduction of a gelling polymer can influence the properties of the network as well as the compatibility of the resulting materials with different cell types. A series of hydrogel compositions consisting of combinations of Fmoc-Lys-Fmoc and Fmoc-Gly-Gly-Gly with Agarose and Phytagel are thus obtained. All compositions form structured gels as shown by rheological studies and scanning electron microscopy. Fourier transform infrared spectroscopy analysis evidences the formation of H-bonds between the polysaccharides and amino acids or short peptides. Moreover, all gels exhibit good cell viability on fibroblasts as demonstrated by a live-dead staining test and good in vivo biocompatibility, which highlights the great potential of these biomaterials for biomedical applications. 相似文献
309.
Dr. Roshni Malde Dr. Daniel A. Richards Luigia Salerno Yanbo Zhao Dr. Kersti Karu Prof. Vijay Chudasama Prof. James R. Baker 《European journal of organic chemistry》2023,26(19):e202201372
Herein we report on photodecarboxylations of various substituted maleimides, resulting in an elimination reaction. Furthermore, we establish facile wavelength tunability through modulation of the maleimide double bond substituents. We envisage that these versatile reagents, which are readily constructed and diversified by nucleophilic substitution reactions on bromomaleimides, will offer new opportunities for triggered photorelease. 相似文献
310.
G. Primofiore A. M. Marini S. Salerno F. Da Settimo D. Bertini L. Dalla Via 《Journal of heterocyclic chemistry》2005,42(7):1357-1361
The preparation and the cytotoxic properties of new derivatives of the planar pyrido[3′,2′:5,6]thiopyrano‐[4,3‐c]pyrazole system, carrying an arylic side group in the 1 or 2 positions, are described. The novel substituted derivatives were obtained by reaction of suitable arylhydrazines with the appropriate key intermediate 3‐hydroxymethylene‐2,3‐dihydrothiopyrano[2,3‐b]pyridin‐4(4H)‐ones. Moreover the preparation was reported of the 2‐carboxamidophenyl derivatives, which was accomplished from the previously obtained pyrido[3′,2′:5,6]thiopyrano[4,3‐c]pyrazole nucleus, by reaction with phenylisocyanate. All the new compounds were evaluated for their antiproliferative ability, by an in vitro assay on human tumor cell lines (HL‐60 and HeLa). 相似文献