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61.
Infra-Red spectra of a series of substituted salicylaldehyde and 2-hydroxy-naphthaldehyde Schiff bases were used to investigate enol-keto tautomeric equilibrium. Two model compounds, namely, salicylidinaniline and naphthylidinequinolineamine Schiff bases were used to represent the enol and keto forms, respectively. From the IR spectra of the model compounds it was possible to assign the IR absorption for the C=O and the C=N groups in both the keto and the enol form. It was also possible to assign other absorptions which were either specific to the keto or the enol forms. Specific pattern were observed for all the studied compounds. 相似文献
62.
The polymeric coordination compounds have been synthesized using the dipotassium salt of N,N′‐di(carboxymethylene)terephthalaldehydediimine (K2SB1) or N,N′‐di(carboxyethylene)terephthalaldehydediimine (K2SB2) with manganese(II), cobalt(II), nickel(II), copper(II), zinc(II), and cadmium(II). The ligands have been characterized by 1H‐NMR, and 13C‐NMR spectra. The polychelates have been characterized by elemental analyses, magnetic measurements, thermogravimetric analyses, electronic spectra and infrared spectra. The coordination compounds are colored, and the central metal ions are octahedrally coordinated with two water molecules and the Schiff bases. The Schiff bases act as di‐negative tetradentate ligands, in which bonding occurs through two oxygen and two nitrogen atoms. The polymers are insoluble in all common organic solvents such as acetone, methanol, ethanol, N,N‐dimethylformamide and dimethylsulfoxide. 相似文献
63.
64.
In this paper we study an instance of projective Reed–Muller type codes, i.e., codes obtained by the evaluation of homogeneous polynomials of a fixed degree in the points of a projective variety. In our case the variety is an important example of a determinantal variety, namely the projective surface known as rational normal scroll, defined over a finite field, which is the basic underlining algebraic structure of this work. We determine the dimension and a lower bound for the minimum distance of the codes, and in many cases we also find the exact value of the minimum distance. To obtain the results we use some methods from Gröbner bases theory. 相似文献
65.
General acid‐catalyzed reaction can be enhanced by the addition of base. Self‐catalyzed esterification of benzoic acid and octan‐1‐ol was enhanced by the addition of certain base such as imidazole. The rate of the esterification was accelerated as the concentration of imidazole increased. Trans‐esterification of 4‐nitrophenyl acetate was promoted in chloroform by the mixture of benzoic acid and imidazole, but not by benzoic acid or imidazole alone. 相似文献
66.
I. Kraicheva P. Finocchiaro S. Failla 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2345-2354
The synthesis of three novel 5-methylfuryl-containing Schiff bases: N,N′-bis(5-methylfurfurylidene)-4,4′-diaminodiphenylmethane, N,N′-bis(5-methylfurfurylidene)-1,4-phenylenediamine, and N,N′-bis(5methylfurfurylidene)benzidine and the corresponding bis(aminophosphonates) derived from them, 4,4′-bis{N-methyl(diethoxyphosphonyl)-1-[(5-methyl)-2-furyl]} diaminodiphenylmethane, 1,4-bis { N-methyl(diethoxyphosphonyl)-1-[(5-methyl)-2-furyl]} diaminobenzene, and bis{N-methyl(diethoxyphosphonyl)-1-[(5-methyl)-2-furyl]}- benzidine, is reported. The compounds have been characterized by elemental analysis, TLC, IR, and NMR ( 1 H, 13 C, and 31 P) spectra. For comparison, new 13 C and 31 P NMR data of three furyl-containing analogues of the above bis(aminophosphonates) are also regarded. The NMR studies of the two series of bis(aminophosphonates) reveal the presence of one diastereomer (meso or racemic form). 相似文献
67.
68.
Hader A. Elgendy 《代数通讯》2019,47(7):2798-2809
69.
Poul Erik Hansen Bahjat A. Saeed Rita S. Rutu Teobald Kupka 《Magnetic resonance in chemistry : MRC》2020,58(8):750-762
1J(15N,H) coupling constants for enaminones and NH-forms of intramolecularly hydrogen-bonded Schiff bases as model compounds for sp2-hybridized nitrogen atoms are evaluated using density functional theory (DFT) to find the optimal functionals and basis sets. Ammonia is used as a test molecule and its one-bond coupling constant is compared with experiment. A methylamine Schiff base of a truncated molecule of gossypol is used for checking the performance of selected B3LYP, O3LYP, PBE, BHandH, and APFD density functionals and standard, modified, and dedicated basis sets for coupling constants. Both in vacuum and in chloroform, modeled by the simple continuum model of solvent, the modified basis sets predict significantly better the 1J(15N,H) value in ammonia and in the methylamine Schiff base of a truncated molecule of gossypol than the standard basis sets. This procure is then used on a broad set of intramolecularly hydrogen-bonded molecules, and a good correlation between calculated and experimental one-bond NH coupling constants is obtained. The 1J(15N,H) couplings are slightly overestimated. The calculated data show for hydrogen-bonded NH interatomic distances that the calculated values depend on the NH bond lengths. The shorter the bond lengths, the larger the 1J(15N,H). A useful correlation between 1J(15N,H) and NH bond length is derived that enables realistic predictions of one-bond NH coupling constants. The calculations reproduce experimentally observed trends for the studied molecules. 相似文献
70.
Synthesis,spectroscopic characterization,thermal behaviour,in vitro antimicrobial and anticancer activities of novel ruthenium tricarbonyl complexes containing monodentate V‐shaped Schiff bases
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The interaction of Ru3(CO)12 with a novel family of monodentate V‐shaped Schiff base ligands (L1–4; L1: (E)‐1‐(4‐((4‐bromobenzylidene)amino)phenyl)ethanone, L2: (E)‐1‐(3‐(4‐(dimethylamino)benzylideneamino)phenyl)ethanone, L3: (E)‐1‐(4‐(4‐(dimethylamino)benzylideneamino)phenyl)ethanone, L4: (E)‐1‐(3‐(3,4‐dimethoxybenzylideneamino)phenyl)ethanone) in air under atmospheric pressure afforded the novel complexes [Ru(CO)3(L1–4)2]. The parent ligands and their complexes were characterized using elemental analyses and spectroscopic techniques. In addition, the structure of the representative ligand L1 was determined using single‐crystal X‐ray analysis. The stereochemistry and theoretical optimization of the three‐dimensional geometry of the ligands and their complexes were justified. In vitro antimicrobial screening against bacterial stains Escherichia coli and Staphylococcus aureus and fungus Candida albicans was conducted. Cytotoxicity of the compounds as anti‐tumour agents was evaluated against liver carcinoma (HepG2), breast carcinoma (MCF7) and colon carcinoma (HCT‐116) cell lines relative to cisplatin and doxorubicin. The complexes showed variable in vitro cytotoxic activities against the three studied cell lines, with IC50 values less than those of cis‐platin, and thus appear to be building blocks for promising anti‐tumour agents. 相似文献