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131.
Osman Yilmaz Ali Usanmaz Kemal Alyürük 《Journal of polymer science. Part A, Polymer chemistry》1993,31(13):3205-3211
n-Butyl isocyanate (nBIC) was polymerized in bulk by the Pruitt–Baggett adduct (PBA) at ?23, 0.0, and 25.0°C. Polymerization was accompanied by trimerization to the cyclicisocyanurates at all temperatures. Spectroscopic evidences supported the nylon-1 structure for both trimer and polymer. The polymer/trimer ratio and the molecular weight of produced polymers were found to increase with decreasing temperature. The Pruitt–Baggett catalyst (PBC), which is the reaction product of (PBA + H2O) system, also polymerized nBIC, but with a relatively slower rate. In aromatic and etheric solutions, nBIC was only trimerized by PBA. Copolymerization of nBIC with propylene oxide by PBA and PBC failed. Some selected monoisocyanates were also polymerized by PBA. © 1993 John Wiley & Sons, Inc. 相似文献
132.
利用水热技术合成了2个新型钴支撑的磷钼多金属氧酸盐超分子化合物:(C2N2H10)5[(P4Mo6O25(OH)6)2Co](1)和(Co(H2O)6)2(C5NH6)6[(P4Mo6O25(OH)6)2Co]·10H2O(2).并通过元素分析、红外光谱、热重分析和X射线单晶衍射对2个化合物进行了表征.结果表明:化合物1属于三斜晶系,P-1空间群;晶胞参数a=1.179 9(2)nm,b=1.337 7(2)nm,c=1.479 7(3)nm,α=73.435(2)°,β=74.383(2)°,γ=66.499(2)°,V=2.020 5(6)nm3,F(000)=1 327,Z=1;化合物2属于属于三斜晶系,P-1空间群;晶胞参数a=1.220 68(11)nm,b=1.381 08(13)nm,c=1.687 18(15)nm,α=92.275(1)°,β=104.774(1)°,γ=114.475(1)°,V=2.468 8(4)nm3,F(000)=1 649,Z=1. 相似文献
133.
As part of our on-going effort to develop 64Cu-based radiopharmaceuticals for PET (positron emission tomography) imaging of multidrug resistance in cancer, we prepared a tetramethylfuranone-functionalized diiminedioxime ligand, TMFPreH (TMFPreH = 4-[3-(4-hydroxyimino-2,2,5,5-dimethyl-dihydro-furan-3-ylideneamino)-propylimino]-2,2,5,5-tetramethyl-dihydrofuran-3(2H)-one oxime) and its Cu(II) and Ni(II) complexes. When the copper(II) complex was prepared from Cu(ClO4)2 in ethanol, it was isolated as a Cu(II)-bridged dimer, but when it was prepared from Cu(OAc)2 and heated in acetone, an unusual example of an acetone adduct of the ligand is formed by reduction of one of the imine double bonds by the solvent. The Ni(II) complex is square pyramidal with the perchlorate counterion at the apex. 相似文献
134.
Esmeralda Rosa Angel Guerrero Mª Pilar Bosch Luis Julià 《Magnetic resonance in chemistry : MRC》2010,48(3):198-204
Photolysis of trifluoromethyl ketones (TFMKs) 1a–1e versus the non‐fluorinated ketones 2a–2b in the presence of radical initiators by electron paramagnetic resonance spectroscopy has been studied for the first time. The transient radicals generated after irradiation of the ketones were identified by trapping with 2‐methyl‐2‐nitrosopropane (MNP) and 2,4,6‐tri‐tert‐butylnitrosobenzene (TTBNB) as spin traps. TTBNB is a powerful, particularly useful spin trap in these kinds of processes producing anilino and nitroxyl spin adducts due to the ambivalent reactivity on the N and O atoms. In the presence of t‐butylperoxide, short‐chain TFMKs, such as 1,1,1‐trifluoroacetone (1d) and hexafluoroacetone (1e), give rise to detection of the elusive trifluoromethyl radical. In contrast, long‐chain TFMKs did not provide clues to prove formation of the trifluoromethyl radical but instead to radicals derived by abstraction of one α‐methylene proton to the carbonyl. Although TFMKs are quite stable to photodegradation in the absence of initiator, methyl ketone 2b and phenyl ketone 3 produce radicals resulting from abstraction of a γ‐hydrogen to the carbonyl group. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
135.
Victoria A. Ivolgina Margarita S. Chernov’yants Leonid D. Popov Vitaliy V. Suslonov Natalya A. Avtushenko Nikolay V. Luanguzov 《Phosphorus, sulfur, and silicon and the related elements》2020,195(5):421-428
AbstractAs a part of investigation of thyreostatic activity of mercapto-substituted triazoles, the structure, spectroscopic properties of 4-amino-5-(furan-2-yl)-4H-1,2,4-triazole-3-thione were obtained. 4-amino-5-(furan-2-yl)-4H-1,2,4-triazole-3-thione forms steady charge-transfer complex in dilute chloroform solution, coordinating one iodine molecule (lgβ?=?3.47). The reaction product of 4-amino-5-(furan-2-yl)-4H-1,2,4-triazole-3-thione is presented by uncharged adduct: C6H6N4OS·I2. The crystal structure of the adduct was studied in detail by single crystal X-ray diffraction. The results of thermogravimetric analysis revealed the stability of adduct in a solid state at the temperature range 50–500?°C. 相似文献
136.
137.
Bernhard Dung Fritz Vögtle 《Journal of inclusion phenomena and macrocyclic chemistry》1988,6(4):429-442
The syntheses of several macrotricyclic hexalactams (1–3) and of a corresponding hexalactone (4) are described in detail for the first time. The molecules have a basket shaped skeleton and contain a non-collapsible cavity, the size and shape of which is varied by use of spacer groups. Compounds1–3 selectively form crystalline adducts with ethanol as guest; the macrotricyclic hexaester4 does not. Evidence for an interaction of1 with ethanol was obtained by exchange experiments with perdeuteroethanol. Complexation experiments in solution did not show significant host/guest interactions with the guest chosen. 相似文献
138.
K. Sivashankar Anupama Ranganathan V. R. Pedireddi 《Journal of Chemical Sciences》2000,112(2):147-151
A complex between cyanuric acid (CA), 4,4′-bipyridyl (BP) and Ag(I), with the composition, [Ag2(C3H2N3O3-κN)2 (C10H8N2-κN)] has been prepared. Crystal structure analysis shows that it has a chain structure in which the CA molecules are linked
to the BP units through silver atoms by the formation of N-Ag-N bonds, wherein one of the hydrogens of CA is replaced by Ag(I),
showing thereby the chains connected to one another by N-H...O hydrogen bonds formed between the CA molecules. This intermolecular
chain structure resembles the chain structure of the CA.BP adduct where CA-BP-CA chains formed by N-H...N hydrogen bonds are
linked to one another by N-H...O hydrogen bonds between the CA molecules. 相似文献
139.
Subban Kathiravan 《Tetrahedron letters》2009,50(45):6116-6120
A one-pot synthesis of ferrocene-grafted dispiropyrrolidine/pyrrolizidine scaffolds has been accomplished in good yields through a facile 1,3-dipolar cycloaddition of various azomethine ylides derived from diketones and secondary amino acids with Baylis-Hillman adduct derived from ferrocene carbaldehyde. The regiochemical and stereochemical outcomes of the cycloaddition reaction were ascertained by X-ray crystallographic studies of one of the cycloadducts. 相似文献
140.
We report the anisotropic linear and second-order nonlinear optical (NLO) properties of arsenic triiodide-octa-sulfur (1:3) adduct, AsI3 · 3S8, which spontaneously crystallizes in the trigonal rhombohedral non-centrosymmetric space group R3m. The trigonal symmetry of the AsI3 · 3S8 molecule coincides with the crystal symmetry. The crystals are optically uniaxial with no/ne of about 1.2 and show dichroism at the UV-visible wavelengths. Second harmonic generation (SHG) tensor elements were determined from Maker fringes measured with an Nd:YAG laser (∼10 ns pulse, 1064 nm). The coefficient d222,eff = 32.0 pm/V for the light polarized parallel to the layers of iodine and sulfur atoms in the AsI3 · 3S8 crystal ab plane is markedly larger than d333 = 11.6 pm/V for the polarization of light parallel to the crystal c axis. The anisotropy parameter, defined as the d222,eff/d333 ratio, is about 2.7 for the AsI3 · 3S8 crystal, smaller than that for the isomorphous CHI3 · 3S8 crystal (7.3) but larger than for the SbI3 · 3S8 crystal (0.7). Highly anisotropic components of the first hyperpolarizability tensor of an AsI3 · 3S8 molecule, β, were derived from the quadratic nonlinear susceptibility tensor of the crystal. 相似文献