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排序方式: 共有195条查询结果,搜索用时 15 毫秒
31.
Predoana Luminita Atkinson Irina Karaj Dániel Attila Odhiambo Vincent Otieno Bakos László Péter Nagyné Kovács Teodóra Pandele-Cusu Jeanina Petrescu Simona Rusu Adriana Szilágyi Imre M. Pokol György Zaharescu Maria 《Journal of Thermal Analysis and Calorimetry》2021,143(4):2893-2900
Journal of Thermal Analysis and Calorimetry - In the literature data, several papers reported the synthesis by various chemical or physical methods of the SrCu2O2 (SCO) having possible applications... 相似文献
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Maricel Agop Stefan Andrei Irimiciuc Adrian Ghenadi Luminita Bibire Stefan Toma Tudor-Cristian Petrescu Dorin Vaideanu Cristina Marcela Rusu Alina Gavrilut Decebal Vasincu 《Entropy (Basel, Switzerland)》2021,23(2)
In the framework of the multifractal hydrodynamic model, the correlations informational entropy–cross-entropy manages attractive and repulsive interactions through a multifractal specific potential. The classical dynamics associated with them imply Hubble-type effects, Galilei-type effects, and dependences of interaction constants with multifractal degrees at various scale resolutions, while the insertion of the relativistic amendments in the same dynamics imply multifractal transformations of a generalized Lorentz-type, multifractal metrics invariant to these transformations, and an estimation of the dimension of the multifractal Universe. In such a context, some correspondences with standard cosmologies are analyzed. Since the same types of interactions can also be obtained as harmonics mapping between the usual space and the hyperbolic plane, two measures with uniform and non-uniform temporal flows become functional, temporal measures analogous with Milne’s temporal measures in a more general manner. This work furthers the analysis published recently by our group in “Towards Interactions through Information in a Multifractal Paradigm”. 相似文献
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Adams CJ Bartlett IM Carlton S Connelly NG Harding DJ Hayward OD Orpen AG Patron E Ray CD Rieger PH 《Dalton transactions (Cambridge, England : 2003)》2007,(1):62-72
The d4 halide complexes [MX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp'] {X=F, Cl, Br or I; R=Me or Ph; M=Mo or W; Tp'=hydrotris(3,5-dimethylpyrazolyl)borate} undergo one-electron oxidation to the d3 monocations [MX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp']+, isolable for M=W, R=Me. X-Ray structural studies on the redox pairs [WX(CO)(eta-MeC[triple bond, length as m-dash]CMe)Tp']z (X=Cl and Br, z=0 and 1), the ESR spectra of the cations [WX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp']+ (X=F, Cl, Br or I; R=Me or Ph), and DFT calculations on [WX(CO)(eta-MeC[triple bond, length as m-dash]CMe)Tp']z (X=F, Cl, Br and I; z=0 and 1) are consistent with electron removal from a HOMO (of the d4 complexes) which is pi-antibonding with respect to the W-X bond, pi-bonding with respect to the W-C(O) bond, and delta-bonding with respect to the W-Calkyne bonds. The dependence of both oxidation potential and nu(CO) for [MX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp'] shows an inverse halide order which is consistent with an ionic component to the M-X bond; the small size of fluorine and its closeness to the metal centre leads to the highest energy HOMO and the lowest oxidation potential. In the cations [MX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp']+ electronegativity effects become more important, leading to a conventional order for Cl, Br and I. However, high M-F pi-donation is still facilitated by the short M-F distance. 相似文献
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Toma LM Lescouëzec R Uriel S Llusar R Ruiz-Pérez C Vaissermann J Lloret F Julve M 《Dalton transactions (Cambridge, England : 2003)》2007,(33):3690-3698
The low-spin iron(III) complex AsPh(4)[Fe(III)(bpy)(CN)(4)].CH(3)CN (1) [AsPh(4) = tetraphenylarsonium cation] and the heterobimetallic chains [{Fe(III)(L)(CN)(4)}(2)Ni(II)(H(2)O)(2)].4H(2)O with L = bpy (2) and phen (3) [bpy = 2,2'-bipyridine and phen = 1,10-phenanthroline] have been prepared and their structures determined by X-ray diffraction methods. The structure of 1 consists of mononuclear [Fe(bpy)(CN)(4)](-) anions, tetraphenylarsonium cations and acetonitrile molecules of crystallization. The iron(III) is hexacoordinated with two nitrogen atoms of the bidentate bpy and four carbon atoms of four terminal cyanide groups building a distorted octahedral surrounding around the metal atom. 2 and 3 are isomorphous compounds whose structure is made up of neutral 4,2-ribbon like bimetallic chains of formula [{Fe(III)(L)(CN)(4)}(2)Ni(II)(H(2)O)(2)] where the [Fe(III)(L)(CN)(4)](-) unit acts as a bis-monodentate bridging ligand toward the trans-diaquanickel(II) units through two of its four cyanide groups in cis positions. The chains exhibit two orientations in the unit cell and they interact with each other through hydrogen bonds involving the coordination and crystallization water molecules together with the uncoordinated cyanide nitrogen atoms of the [Fe(L)(CN)(4)](-) units. Compounds 2 and 3 behave as ferromagnetic Fe(III)(2)Ni(II) chains which interact ferromagnetically at very low temperatures in the case of 2, whereas metamagnetic-like behaviour is observed for with a critical field (H(c)) around 200 G. For H > H(c) the ferromagnetic Fe(III)(2)Ni(II) chains of 3 exhibit a frequency dependence of the out-of-phase ac susceptibility signal at T < 3.5 K. 相似文献
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Pocol V. Patron L. Carp O. Brezeanu M. Segal E. Stanica N. Crisan D. 《Journal of Thermal Analysis and Calorimetry》1999,55(1):143-154
The polynuclear coordination compounds LnCr(tartrate)3·nH2O where Ln(III)=La-Er, obtained through a precipitation method, were characterized on the basis of elemental analysis, their
electronic and vibrational spectra and magnetic susceptibility measurements. The possibility of obtaining chromites through
the transformations of the polynuclear coordination compounds in the solid state was considered. The thermal decompositions
of these compounds, studied by TG and DTA methods, were found to follow an almost uniform pattern. The decompositions occurred
in six-eight steps. The first two steps involved dehydration, and the third the transformation of tartrate anions to oxalate,
followed by conversion to carbonate and oxocarbonate intermediates. The final product in each case was LnCrO3. A non-isothermal kinetic analysis of the first decomposition steps was performed, the most probable decomposition mechanism
being selected and the kinetic parameters evaluated. The final products of the transformations were characterized.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
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Thermoanalytical, mass spectrometric and X-ray diffraction data were associated with a reliable assignation of the thermal
transformations of the coordination compound [Mn(urea)6](NO3)2·2H2O.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
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Theodora-Venera Apostol Luminita Gabriela Marutescu Constantin Draghici Laura-Ileana Socea Octavian Tudorel Olaru George Mihai Nitulescu Elena Mihaela Pahontu Gabriel Saramet Cristian Enache-Preoteasa Stefania-Felicia Barbuceanu 《Molecules (Basel, Switzerland)》2021,26(16)
In order to develop novel bioactive substances with potent activities, some new valine-derived compounds incorporating a 4-(phenylsulfonyl)phenyl fragment, namely, acyclic precursors from N-acyl-α-amino acids and N-acyl-α-amino ketones classes, and heterocycles from the large family of 1,3-oxazole-based compounds, were synthesized. The structures of the new compounds were established using elemental analysis and spectral (UV-Vis, FT-IR, MS, NMR) data, and their purity was checked by reversed-phase HPLC. The newly synthesized compounds were evaluated for their antimicrobial and antibiofilm activities, for toxicity on D. magna, and by in silico studies regarding their potential mechanism of action and toxicity. The 2-aza-3-isopropyl-1-[4-(phenylsulfonyl)phenyl]-1,4-butanedione 4b bearing a p-tolyl group in 4-position exhibited the best antibacterial activity against the planktonic growth of both Gram-positive and Gram-negative strains, while the N-acyl-α-amino acid 2 and 1,3-oxazol-5(4H)-one 3 inhibited the Enterococcus faecium biofilms. Despite not all newly synthesized compounds showing significant biological activity, the general scaffold allows several future optimizations for obtaining better novel antimicrobial agents by the introduction of various substituents on the phenyl moiety at position 5 of the 1,3-oxazole nucleus. 相似文献