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61.
Ga‐Young Lee Jin‐Hyang Kim Hyo Jin No Ju‐Yeon Lee Bum Ku Rhee Hee‐dok Choi 《Journal of polymer science. Part A, Polymer chemistry》2009,47(7):1911-1919
1‐{3,4‐Di‐(2‐hydroxyethoxy)phenyl}‐2‐(2‐thiophenyl)ethene (5) was prepared and condensed with terephthaloyl chloride to yield polyester (6). Polymer 6 was reacted with tetracyanoethylene to give a new Y‐type polyester (7) containing 1‐(3,4‐dioxyethoxy)phenyl‐2‐{5‐(2,2,3‐tricyanovinyl)‐2‐thiophenyl)}ethenyl groups as NLO‐chromophores, which are components of the polymer backbones. Polyester 7 is soluble in common organic solvents such as N,N‐dimethylformamide and acetone. Polymer 7 showed a thermal stability up to 300 °C in thermogravimetric analysis with glass transition temperature (Tg) obtained from differential scanning calorimetry near 126 °C. The second harmonic generation (SHG) coefficient (d33) of poled polymer film at the 1560 nm fundamental wavelength was around 6.57 × 10?9 esu. The dipole alignment exhibited high thermal stability up to the Tg, and there was no SHG decay below 125 °C due to the partial main‐chain character of polymer structure, which is acceptable for NLO device applications. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1911–1919, 2009 相似文献
62.
A scaling equation of state giving a realistic ratio of Curie–Weiss constants and accounting for coupling of the order parameter with a strain (secondary order parameter) is used to describe the temperature dependence of the electric susceptibility in an external biasing field applied in case of uniaxial ferroelectrics. Explicit expressions for the resulting scaling invariants are given. The power laws for the temperature and field dependence of the maxima and of the inflection points of the susceptibility curves are found. The theory is exemplified by the effective critical behaviour of iono-molecular crystals (CH3NH3)5Bi2Cl11 (MAPCB) and (CH3NH3)5Bi2Br11 (MAPBB). 相似文献
63.
Species of the genus Cystoseira are particularly hard to discriminate, due to the complexity of their morphology, which can be influenced by their phenological state and ecological parameters. Our study emphasized on the relevance of two kinds of analytical tools, (1) LC/ESI-MSn and (2) 1H HR-MAS NMR, also called in vivo NMR, to identify Cystoseira specimens at the specific level and discuss their taxonomy. For these analyses, samples were collected at several locations in Brittany (France), where Cystoseira baccata, C. foeniculacea, C. humilis, C. nodicaulis and C. tamariscifolia were previously reported. To validate our chemical procedure, the sequence of the ITS2 has been obtained for each species to investigate their phylogenetic relationships at a molecular level. Our study highlighted the consistency of the two physico-chemical methods, compared to “classical” molecular approach, in studying taxonomy within the genus Cystoseira. Especially, LC/ESI-MSn and phylogenetic analyses converged into the discrimination of two taxonomical groups among the 5 species. The occurrence of some specific signals in the 1H HR-MAS NMR spectra and/or some characteristic chemical compounds during LC/ESI-MSn analysis could be regarded as discriminating factors. LC/ESI-MSn and 1H HR-MAS NMR turned out to be two relevant and innovative techniques to discriminate taxonomically this complex genus. 相似文献
64.
Sharma SK Roudaut G Fabing I Duplâtre G 《Physical chemistry chemical physics : PCCP》2010,12(42):14278-14284
The triplet state of positronium, o-Ps, is used as a probe to characterize a starch-20% w/w sucrose matrix as a function of temperature (T). A two-step decomposition (of sucrose, and then starch) starts at 440 K as shown by a decrease in the o-Ps intensity (I(3)) and lifetime (τ(3)), the latter also disclosing the occurrence of a glass transition. Upon sucrose decomposition, the matrix acquires properties (reduced size and density of nanoholes) that are different from those of pure starch. A model is successfully established, describing the variations of both I(3) and τ(3) with T and yields a glass transition temperature, T(g) = (446 ± 2) K, in spite of the concomitant sucrose decomposition. Unexpectedly, the starch volume fraction (as probed through thermal gravimetry) decreases with T at a higher rate than the free volume fraction (as probed through PALS). 相似文献
65.
Zusammenfassung Die Jodidoxydation durch Cu(II) wird in Anwesenheit von Ammoniak, Natriumtartrat, citrat oder -oxalat infolge Komplexbildung verhindert. Daher kann man z. B. Quecksüber(II) in Anwesenheit der genannten Komplexbildner mit Kaliumjodid maskieren und Kupfer(II) durch direkte Titration mit ÄDTA gegen Murexid, Brenzcatechinviolett, Chromazurol S, PAN oder PAR als Indikator bestimmen.
Masking with potassium iodide in direct titrations of copper(II) with ethylenediamine tetraacetic acid
Summary The formation of a complex prevents the iodide oxidation by Cu(II) in the presence of ammonia, sodium tartrate, citrate, or oxalate. Hence mercury(II) for instance, can be masked against potassium iodide in the presence of these complex formers, and Cu(II) can be determined by direct titration with EDTA in the presence of murexide, pyrocatechol violet, chromazurol, PAN or PAR as indicator.相似文献
66.
Gaël Rouillé Dr. Cornelia Jäger Dr. Mathias Steglich Friedrich Huisken Prof. Dr. Thomas Henning Prof. Dr. Gabriele Theumer Ingmar Bauer Dr. Hans‐Joachim Knölker Prof. Dr. 《Chemphyschem》2008,9(14):2085-2091
The spectroscopic characterization of corannulene (C20H10) is carried out by several techniques. The high purity of the material synthesized for this study was confirmed by gas chromatography‐mass spectrometry (GC‐MS). During a high‐performance liquid chromatography (HPLC) process, the absorption spectrum of corannulene in the ultraviolet (UV) and visible (vis) ranges is obtained. The infrared (IR) absorption spectrum is measured in CsI pellets, and the Raman scattering spectrum is recorded for pure crystal grains. In addition to room temperature measurements, absorption spectroscopy in an argon matrix at 12 K is also performed in the IR and UV/Vis ranges. The experimental spectra are compared with theoretical Raman and IR spectra and with calculated electronic transitions. All calculations are based on the density functional theory (DFT), either normal or time‐dependent (TDDFT). Our results are discussed in view of their possible application in the search for corannulene in the interstellar medium. 相似文献
67.
Derrien G Charnay C Zajac J Jones DJ Rozière J 《Chemical communications (Cambridge, England)》2008,(27):3118-3120
Copper-containing mesoporous silica spheres of size in the colloidal range with perfect conservation of pore-ordering, shape and monodispersity and high intra-pore metal dispersion were prepared via a new one-step synthesis and functionalisation route. 相似文献
68.
Dr. Gaël Rouillé Mathias Steglich Dr. Cornelia Jäger Prof. Dr. Friedrich Huisken Prof. Dr. Thomas Henning Gabriele Theumer Dr. Ingmar Bauer Prof. Dr. Hans‐Joachim Knölker 《Chemphyschem》2011,12(11):2131-2137
We report on the characterization of dibenzo[cde,opq]rubicene (C30H14). The molecule was studied in solution at room temperature with absorption spectroscopy in the visible (vis) and ultraviolet (UV) wavelength ranges, and with emission spectroscopy. The infrared (IR), visible, ultraviolet, and vacuum ultraviolet (VUV) absorption spectra of a thin film were measured also at room temperature. In addition, the UV/vis absorption spectrum was measured at cryogenic temperatures using the matrix isolation spectroscopy technique. The interpretation of spectra was supported by theoretical calculations based on semiempirical and ab initio models, as well as on density functional theory. Finally, the results of the laboratory study were compared with interstellar spectra. 相似文献
69.
Dr. Pavlína Košinová Dr. Radek Gažák Prof. Jean‐Luc Duroux Prof. Roberto Lazzaroni Prof. Vladimír Křen Prof. Xavier Assfeld Dr. Patrick Trouillas 《Chemphyschem》2011,12(6):1135-1142
Natural polyphenols are known to be oxidized by free radicals, which partially explains the antioxidant properties of a number of these compounds. This oxidation may also be used to synthesise new compounds of biological interest, for example, dimers. The present theoretical study describes the existing experimental evidence showing that silybin and dehydrosilybin [natural polyphenols isolated from milk thistle (Silybum marianum)] form dimers regioselectively. Based on DFT calculations, thermodynamic and kinetic values were computed in order to better understand the physicochemical behaviour of these dimerisation processes. Calculations showed that after H‐atom transfer (from polyphenol to radical), dimerisation could proceed in two steps: 1) bond formation and, when possible, 2) tautomerisation reorganisation. The former step is the limiting step, while the latter is crucial for the process to be thermodynamically favourable (ΔG<0). If this rearrangement is impossible then dimerisation is not feasible, or at least becomes a minor process (e.g., dehydrosilybin dimerisation after H‐atom abstraction from the 3‐OH group). This explains the regioselectivity of polyphenol dimerisation. 相似文献