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71.
Guangdong Zhou Tiexin Cheng Wenxing Li Yingli Bi Kaiji Zhen 《Reaction Kinetics and Catalysis Letters》2003,79(2):295-302
Polyaniline(PAN) supported H6P2W18O62(PW) , H3PMo12O40 (PMo) and H4PMo11VO40(PMoV) catalysts were prepared and their activities for hexanol conversion were tested. IR, XRD, ICP and SEM measurements
proved that the heteropolyacids (HPA) could be supported on this type of polymer. The PAN supported HPA catalysts exhibit
higher redox activities and low acid-base activities for the hexanol conversion. The redox activities increase with increasing
amount of the heteropolyacid. Substitution of Mo ion by V ion results in an increase of redox activities of the catalysts.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
72.
Chun‐Bo Liu Guang‐Bo Che Chuan‐Bi Li Yun‐Cheng Cui 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):m153-m155
An in situ reaction under hydrothermal conditions leads to the formation of the title compound, diaqua(pyridine‐2‐carboxylato)(pyridine‐2,6‐dicarboxylato)indium(II) trihydrate, [In(C6H4NO2)(C7H3NO4)(H2O)2]·3H2O, in which the central InIII atom is seven‐coordinated by one pyridine‐2,6‐dicarboxylate ligand, one pyridine‐2‐carboxylate ligand and two water molecules in a pentagonal–bipyramidal coordination environment. An indium(III)–water chain based on an unusual water pentamer is observed. 相似文献
73.
The CO_2 laser induced room temperature reactions of CH_3CF_2H or another protium-donorCH_3CHClCH_3 with chlorine-atom donors (Z--Cl) CFCl_2CF_2Cl, CF_3CCl_3, CFCl_3 or CF_2Cl_2, havebeen investigated. Some of these reactions can yield two important monomers (CF_2=CH_2 andCF_2=CFCl) for fluoropolymers simultaneously. The yield dependence of these two alkenes on experi-mental conditions has been studied. A laser-initiated chain process is supported by identifica-tion of Z--H intermediates in these reactions. 相似文献
74.
Yao‐Cheng Shi Bei‐Bei Zhu Xiao‐Bi Jing 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(11):m559-m562
The molecules of N,N′‐bis(2‐pyridylmethyl)ferrocene‐1,1′‐diyldicarboxamide, [Fe(C12H11N2O)2], contain intramolecular N—H⋯N hydrogen bonds and are linked into sheets by three independent C—H⋯O hydrogen bonds. The molecules of the isomeric compound N,N′‐bis(3‐pyridylmethyl)ferrocene‐1,1′‐diyldicarboxamide lie across inversion centres, and the molecules are linked into sheets by a combination of N—H⋯N hydrogen bonds and π–π stacking interactions between pyridyl groups. 相似文献
75.
P. De Bièvre 《Accreditation and quality assurance》2000,5(6):224-230
Traceability is a property of the result of a measurement. Since values carried by (reference) materials must also have been
obtained, of necessity, by measurement, the definition of traceability also applies to reference materials. It is extremely
helpful to give the traceability (of the origin) of a reference material a separate name, i.e. 'trackability'. An analysis
of the function of values carried by reference materials, shows that they can fulfill different functions, depending on the
intended use. One of the functions located outside the traceability chain – and hence not very relevant for establishing traceability
– is evaluating the approximate size of the uncertainty of the measurement of an unknown sample by performing a similar measurement
on a reference material, used as a 'simulated sample'. Another function is located inside the traceability chain, where the
reference material is used as an added 'internal standard'. Then, the value carried by the reference material is essential
for establishing the traceability of the measured value of an unknown sample. In the latter application, the reference material
acts as an 'amount standard' (the certified value for amount is used).
Received: 11 November 1999 / Accepted: 24 February 2000 相似文献
76.
Reaction of PdCl2(CH3CN)2 with the sodium salt of 5‐mercapto‐1‐methyltetrazole (MetzSNa) in methanol solution affords an interesting dinuclear palladium complex [Pd2(MetzS)4 ] ( 1 ). However, treatment of PdCl2(CH3CN)2 with neutral MetzSH ligand in methanol solution produces a mononuclear palladium complex [Pd(MetzSH)4]Cl2 ( 2 ). Both complexes were characterized by IR, 1HNMR, UV‐Vis spectroscopy as well as X‐ray crystallography. Single‐crystal X‐ray diffraction analyses of two complexes lead to the elucidation of the structures and show that 1 possesses an asymmetric structure: one Pd atom is tetracoordinated by three sulfur atoms and one nitrogen atom to form PdS3N coordination sphere, the other Pd atom is tetracoordinated by three nitrogen atoms and one sulfur atom to form PdSN3 coordination sphere. The molecules of 1 are associated to 1‐D infinite linear chain by weak intermolecular Pd···S contacts in the crystal lattice. In 2 , the Pd atom lies on an inversion center and has a square‐planar coordination involving the S atoms from four MetzSH ligands. The two chloride ions are not involved in coordination, but are engaged in hydrogen bonding. 相似文献
77.
Zhenchuan Wen Xuejian Ma Xiaoyu Yang Pengqing Bi Mengsi Niu Kangning Zhang Lin Feng Xiaotao Hao 《中国化学快报》2019,30(5):995-999
In this work, the donor:acceptor ratio effected photophysical properties of non-fullerene organic solar cells are comparatively investigated. Effective transportation of the photo-generated charge carriers can be obtained with the PDBD-T:ITIC ratio variation. There is no significant energy loss variation exists in the process of changing the D:A ratio. 相似文献
78.
Gao D Tian Y Bi S Chen Y Yu A Zhang H 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):1203-1208
The interactions of colloidal gold and serum albumins, including bovine serum albumin (BSA) and human serum albumin (HSA), were studied by fluorescence and absorption spectrometry. Fluorescence quenching spectrometry was applied to study the interactions between colloidal gold and serum albumins. At pH 7.4 phosphate-buffered saline (PBS), the intensity of fluorescence emission spectrum of serum albumins decreased in the presence of colloidal gold, which indicated that colloidal gold quenched the fluorescence of serum albumins. Experimental results indicated that the combination reactions of colloidal gold and serum albumins were static quenching processes. Based on the effect of colloidal gold on fluorescence intensity, the binding constants, the numbers of binding sites and the acting forces between colloidal gold and serum albumins were found. 相似文献
79.
Wen Weng Qing Le Zeng Bi Xia Yao Wen Shi Lin Qing Hua Wang Xiu Li You 《Chromatographia》2006,64(7-8):463-467
Five structurally related amino acid derivatives were enantioseparated by HPLC with a commercially available chiral stationary phase, Chiralcel OD-H. The chromatographic experiments were performed in the normal phase mode. n-Hexane/polar alcohol was used as mobile phase. Excellent baseline enantioseparations could be obtained for all these solutes. The effects of the concentration of polar alcohol and the column temperature on the retentions and enantioseparations were studied in detail. From the van't Hoff plots the corresponding apparent thermodynamic parameters were derived. Mechanism aspects of chiral recognition were discussed based on the relationship between the thermodynamic parameters and the structures of the solutes. It was found that the substituent of the phenyl group on the residual group of the amino acid derivatives was close relevant to thermodynamic origin of enantioseparation. Much better enthalpy–entropy compensation effect was obtained by plotting the differential, rather than the original, thermodynamic parameters. 相似文献
80.
Seven structurally related amino acid derivatives were successfully enantioseparated by HPLC with a commercially available column containing a chiral immobilized network polymer derived from L-tartaric acid. The experiments were carried out under normal-phase conditions. All the solutes could be baseline separated using n-hexane/2-propanol (95/5) as eluent at a flow rate of 1 ml/min at 25 degrees C, with reasonable retention time (<12 min). The effects of the polar alcohol modifier (type and content) in the mobile phase and the column temperature on the enantioseparation were studied. Apparent thermodynamic parameters were also calculated from the plots of ln alpha or ln k' versus 1/T. Some mechanistic aspects of chiral recognition were discussed with respect to the structures of the solutes. It was found that the enantioseparations are all enthalpy driven, and the N-acyl groups of the solutes have significant influence on the chiral recognition. 相似文献