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71.
Adam Huczyski Daniel owicki Bogumil Brzezinski Franz Bartl 《Journal of Molecular Structure》2008,879(1-3):14-24
A new 2-(2-methoxyethoxy)ethyl ester of Monensin A (MON7) has been synthesized and its capability of complex formation with Li+, Na+, and K+ cations has been studied by ESI MS, 1H and 13C NMR, FT-IR, and PM5 semiempirical methods. ESI mass spectrometry indicates that MON7 forms complexes with Li+, Na+, and K+ of exclusively 1:1 stoichiometry which are stable up to cv = 70 V. The formation of complexes between MON7 and Na+ cations is strongly favored. Starting from about cv = 90 V fragmentation of the respective complexes is observed, primarily characterized by several dehydration steps. The structures of the MON7 complexes with Li+, Na+, and K+ cations are stabilized by intramolecular hydrogen bonds in which the OH groups are always involved. The structures are visualized and discussed in detail. It has been proved that the formation of a pseudo crown ring structure formed by MON7 is preferred in complexes with Na+ cations. 相似文献
72.
Heinz Falk Helmut Marko Norbert Müller Wolfgang Schmitzberger Hugo Stumpe 《Monatshefte für Chemie / Chemical Monthly》1990,121(11):893-901
Summary Apomyoglobin was reconstituted with bile pigments of the verdinoid, 2,3-dihydroverdinoid, pterobilinoid, and violinoid type. Absorption and circular dichroism data as well as formation constants of the complexes were measured. From these results it was concluded that chromophore binding and induced chirality of these pigments are mainly governed by a lipophilic region opposite to the propionic side chain(s) and the asymmetric position of the hydrogen bonding acceptors of the propionic acid side chain(s) at the entrance of the protein pocket.Dedicated to Prof. Dr. A. Eschenmoser on occasion of his 65th birthday 相似文献
73.
Gerd Meyer Prof. Dr. 《无机化学与普通化学杂志》2008,634(15):2729-2736
74.
We compute Hölder Complexes, i.e. the complete bi-Lipschitz invariants, for germs of real weighed homogeneous algebraic or semialgebraic surfaces. 相似文献
75.
Some binary and ternary complexes of Ni(II) with arylideneanthranilic acids and Lewis bases have been prepared and characterized by elemental analyses, IR spectra and X-ray powder diffraction. On the basis of the IR spectra it was found that the Schiff bases used act as monobasic bidentate ligands except for the ortho-hydroxy derivative which acts as a dibasic tridentate ligand. From X-ray analysis it is concluded that the binary Ni(II) chelates are isostructural, and the ternary Ni(II) complexes are also isostructural. 相似文献
76.
77.
Francisco Hueso-Urea Miguel N. Moreno-Carretero Antonio L. Peas-Chamorro Jos M. Amig Vicente Esteve Tony Debaerdemaeker 《Polyhedron》1999,18(27):1666-3636
From reactions between different Cu(II) salts and the Schiff base 6-amino-5-formyl-1,3-dimethyluracil-benzoylhydrazone (H2BEZDO) in alcohol, six new copper complexes with simplified formulas [Cu(HBEZDO)(H2O)(MeOH)]NO3 (1), [CuCl(HBEZDO)(DMF)] (2), [CuBr(HBEZDO)]·2H2O (3), CuBr(HBEZDO) (4), Cu(ClO4)(HBEZDO)·H2O (5), and Cu(SO4)1/2(HBEZDO)·1
H2O (6) were isolated. The structures of compounds 1, 2 and 3 have been established by means of XRD diffraction methods. In the three compounds, the Schiff base acts as a tridentate monodeprotonated ligand through the N(6), N(51) and O(52) atoms, making two five- and six-membered chelate rings. In the structure of 1 and 2, the solvent molecules are coordinated giving square-based pyramidal environments, with the basal plane completed by a MeOH (1) or Cl (2) and the apical positions occupied by the oxygen atom of a water (1) or a DMF molecule (2). The molecular unit of the complex [CuBr(HBEZDO)]·2H2O (3) is defined by a square-plane containing the three donor atoms of the organic ligand and a bromide ligand (Cu–Br 2.384 Å), but there is a stronger tetragonally elongated pyramidal geometry around the metal, the apical position of the polyhedron being occupied by a weakly bound-to-copper bromine atom (3.086 Å) of a neighbouring molecule. This fact gives the appearance of an apparent dimer with very asymmetric bromine bridges, in which there are no exchange interactions between metal centres. Also, infrared, magnetic and EPR data of the isolated complexes are reported. 相似文献
78.
《Journal of Coordination Chemistry》2012,65(7):571-577
A direct synthetic method of mixing Bi(NO3)3 and NaI with 1,10-phenanthroline yielded red crystals of [Bi2(phen)4(NO3)4.4I0.6]I3. In this complex the cationic part is in fact binuclear and contains two [Bi(phen)(NO3)1.7I0.3] groups linked via a bridging NO? 3 anion. The I? 3 anion was not coordinated to bismuth(III) and the lone pair of valence electrons of the bismuth(III) ions appears to be stereochemically inactive. There are two independent NO? 3 anions, one coordinated to bismuth but another shares a position with I? anion. The final results of crystallography show that 40% of these positions are occupied by NO? 3 anions and 60% by I? anions that are coordinated to bismuth atom in bidentate fashion (NO? 3) and in unidentate fashion (I?). An interesting point is that the I? 3 anion was produced by direct synthetic method (Branched tube method). There is a π-π stacking interaction between the parallel aromatic rings around the Bi(III) ion. 相似文献
79.
Leonardo M. PereiraWagner A. Alves 《Vibrational Spectroscopy》2011,56(2):250-254
Raman experiments of formamide and zinc chloride solutions in a wide concentration range (0.1-5.0 mol kg−1) have been carried out. The spectral changes were interpreted on three different ways: (i) the rupture of the H-bonds of FA was evidenced by the trend observed in the νCO, δHNH and restricted (translation or libration) modes; (ii) the appearance of a new band in the νCN region (∼1338 cm−1) was assigned to FA coordinated to Zn (II) through nitrogen atom; (iii) the electronic delocalization in the FA structure upon complexation provided the appearance of new features in the δCH and νCH regions. The quantitative treatment performed at the νCN region of FA allowed the determination of an average number of 3 FA molecules per Zn (II) in the first solvation shell. This value is supported by the appearance of features assigned to ZnCl+ and ZnCl2 entities that also occupy vertices of the tetrahedron at higher salt concentrations. The present study may be useful for a better understanding on electrochemical processes employed in the production of dendritic zinc films as well as FA hydrolysis catalyzed by this metal. 相似文献
80.