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131.
Müzeyyen Demirel Gülsel Yurtdaş Lütfi Genç 《Journal of inclusion phenomena and macrocyclic chemistry》2011,70(3-4):437-445
Ketoconazole (KZ) is an imidazole antifungal agent which is administered topically and also orally. KZ is practically insoluble in water. Vaginal candidiasis is a common condition and up to 75% of all women have at least one episode of this infection during their lifetime. The aim of study was to prepare KZ/β-cyclodextrin (β-CD) complex to improve the physicochemical properties of KZ and to investigate the possibility of preparing vaginal suppositories with the complexes. A linear increase in KZ solubility as a function of β-CD concentration was verified using the phase-solubility diagram. The resulting diagram was classified as AL-type, is generally related to the formation of a soluble complex. Complexes were prepared in a 1:1 molar ratio by different methods, namely freeze-drying, spray-drying, co-evaporation and kneading. Characterization of the complexes prepared was performed by practical yield %, aqueous solubility, active agent amount analyses, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffractometry (PXRD) and 1H and 13C nuclear magnetic resonance (NMR) spectroscopy. Characterization studies provided additional evidences of complexation. The paddle method defined in USP31 was used in in vitro dissolution experiments on the prepared vaginal suppositories. It was found that solubility enhancement by preparing KZ/β-CD complexes depends on the type of the preparation method. Dissolution of KZ from complexes was found to be faster than the active agent and the commercial suppositories. This result may be attributed to the interactions between β-CD and active agent, high energetic amorphous state and decrease in the interfacial tension between insoluble active agent and dissolution media. 相似文献
132.
Chemicalc0mponentsofthegenusRhododendronwithvariousbioactivities,suchasantitussiveandantitracheitishavebeenidentifiedbefore'.T0thebestofourkn0wledge,theplantRhododendronlatoucheaeFinetetFranchofthegenushasnotbeenstudiedchemicallyupt0n0w.Wehereinrep0rtthestructuraIelucidationoftw0newnaturalphen0licc0mpoundsnamed( )-rhodolat0uchollandisoepirh0d0dendrin4fromtheleavesofR.laloucheae.Besides,sixotherknownc0mpounds,( )-rh0d0dendr0l2,epirh0d0dendrin3.4-(3'-O-0-D-glucopyranosyl-4'-hy5,4-(4'-O-6-D-g… 相似文献
133.
Xue Mei LUO Wei Jiang HE Yu ZHANG Zi Jian GUO Long Gen ZHU* State Key Laboratory of Coordination Chemistry Nanjing University Nanjing 《中国化学快报》2000,11(11)
Selectively chemical cleavage of peptides and proteins is one of the most important reactions in both chemical and biochemical processes. Over the past decade, the interaction of palladium(II) complexes with methionine, cysteine and histidine-containing peptides and proteins and the hydrolytic cleavage of the corresponding amide bond by Pd(II) complexes have been extensively studied1-13. However, reports concerning the directly selective hydrolysis of peptides and proteins with other simple … 相似文献
134.
S. Shanmuga Sundara Raj Hoong‐Kun Fun Zhong‐Lin Lu Wen Xiao Xiao‐Yang Gong Chang‐Ming Gen 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(8):1013-1014
The crystal structure of the title compound, C15H14N2O2·H2O, is in the keto tautomeric form and the configuration at the azomethine C=N double bond is E. The molecule is non‐planar, with a dihedral angle of 27.3 (1)° between the aromatic rings. The crystal structure is stabilized by extensive hydrogen bonding involving the water molecule and hydrazone moiety. 相似文献
135.
136.
A class of optimal adaptive multi-arm clinical trial designs is proposed based on an extended generalized Pólya urn (GPU) model. The design is applicable to both the qualitative and quantitative responses and achieves, asymptotically, some pre-specified optimality criterion. Such criterion is specified by a functional of the response distributions and is implemented through the relationship between the design matrix and its first eigenvector. The asymptotic properties of the design are studied using the existing methods on GPU. Some examples for commonly used clinical designs are given as illustration. 相似文献
137.
In this study ground and excited states acidic dissociation constants of a recently synthesized Schiff base was obtained in a DMF:water mixture of 30:70 (v/v) using absorption and fluorescent spectra of the Schiff base in different pH values with the aid of chemometric methods. In addition, the fluorescent of the two kinds of tautomers of this Schiff base was investigated and the rate of tautomerization was obtained using rank annihilation factor analysis (RAFA). The effect of different kinds of surfactants such as sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB) and Triton X-100 on fluorescence spectrum of the Schiff base in a DMF:water mixture of 2:98 (v/v) was investigated. CTAB increased the fluorescence intensity of the Schiff base while SDS and Triton X-100 had no significant effect on it. β-Cyclodextrin increased the fluorescence intensity of the Schiff base. Also the sensing behavior of this Schiff base toward metal ions was studied in DMF and ethanol by fluorescence spectroscopy. The Schiff base showed prominent fluorescent signal in the presence of Zn2+, whereas other metal ions failed to induce response and ground-state dissociation constant of the complex was determined by direct fluorimetric titration as a function of Zn2+ concentration. 相似文献
138.
Hasan budak Ahmet Bulut Naziye etin Canan Kazak 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(1):m1-m3
The crystal structure of the first acesulfame–metal complex, namely tetraaquabis[6‐methyl‐1,2,3‐oxathiazin‐4(3H)‐onato 2,2‐dioxide‐κN]cobalt(II), [Co(C4H4NO4S)2(H2O)4], is reported. The CoII ion resides on a twofold axis and is coordinated by four aqua ligands defining the basal plane and by two monodentate acesulfamate ligands, via their ring N atoms, in the axial positions. Two intra‐ and three intermolecular hydrogen‐bonding interactions stabilize the crystal structure and form an infinite three‐dimensional lattice. 相似文献
139.
SincethefirstBarbier-typereacti0ninaqueousmediainl977',organometallicreactionshaveattractedconsiderableattentioninorganicsynthesis'.lfonecanperformorganometallic-typereactionsinaque0usmediajustasgeneralIyandeasilyasin0rganicsoIvents,suchreactionsmay0fferconsiderableadvantagesf(l)Thereisthepracticalconvenienceofnothavingtohandleinflammableandanhydrousorganicsolvents.(2)Thetedioustaskofprotection-deprotectionchemistryforcertainfunctionalgroupsoftenenc0unteredin0rganicsynthesismaynotberequired.(… 相似文献
140.
Jing Qin Guohai Liang Bingxi Feng Gen Wang Na Wu Yonghui Deng Ahmed A. Elzatahry Abdulaziz Alghamdi Yongxi Zhao Jing Wei 《中国化学快报》2021,32(2):842-848
Plant polyphenol-based coordination polymers(CPs) with ultra-small particle size and tailorable compositions are highly desired in biomedical applicatio ns,but their synthesis is still challenging due to the sophisticated coordination assembly process and unavoidable self-oxidation polymerization of polyphenol. He rein,a general ligand covalent-modification mediated coordination assembly strategy is proposed for the synthesis of water-dispersible CPs with tunable metal species(e.g., Gd,Cu,Ni,Zn,Fe)and ultra-small diameter(8.6-37.8 nm) using nontoxic plant polyphenol(e.g..tannic acid,gallic acid) as a polymerizable ligand.Polyphenol molecules react with formaldehyde firstly,which can effectively retard the oxidation induced self-polymerization of polyphenol and lead to the formation of metal ions containing CPs colloidal nanoparticles.These ultrafine nanoparticles with stably chelated metal io ns are highly water dispersible and thus advantageous for bioimaging.As an example,ultra-small Gd contained CPs exhibit higher longitudinal relaxivity(r_1=25.5 L mmol ~1 s ~1) value with low r_2/r_1(1.19) than clinically used Magnevist(Gd-DTPA,r_1=3.7 L mmol ~1 s ~1).Due to the enhanced permeability and retention effect,they can be further used as a positive contrast agent for T_1-weighted MR imaging of tumour. 相似文献