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51.
<正>A new iridoid glucoside,allamanoid(1),was isolated from the aerial parts of Allamanda neriifolia,together with three known glucosides,plumieride,protoplumericin,and nicotiflorin.Their structures were elucidated by 1D and 2D spectroscopic analyses, hydrolysis,and comparison with literature data.  相似文献   
52.
<正>One new dammarane-type triterpene saponin,named(20S)-3β,20,21-trihydroxydammar-24-ene 3-O-[α-L-rhamnopyranosyl- (1→2)][β-D-xylopyranosyl(1→3)]-β-D-glucopyranoside(1),was isolated from the aerial parts of Gynostemma pentaphyllum (Thunb.) Makino.Its structural elucidation was accomplished mainly on the basis of the interrelation of spectroscopic methods, such as IR,HR-TOF-MS,NMR.  相似文献   
53.
The trimeric phenylenevinylene with the symmetrical chiral end-groups(ChTPV) was synthesized.The liquid crystalline and luminescent properties of the ChTPV have been studied by differential scanning calorimetry(DSC),polarized optical microscopy (POM),absorption and photoluminescence spectra.The results indicated that the ChTPV exhibits mesophase over a wide temperature range and a typical optical texture of smectic phase.In contrast with the spectra of the solution,that of the film showed blue-shift in m...  相似文献   
54.
<正>An improved strategy for the synthesis of 3,3'-(oxy-p-phenylene)bis(2,4,5-triphenylcyclopentadienone) was developed,which includes three steps:Friedel-Crafts reaction,oxidation and condensation.Importantly,the use of KMnO_4 made the second step simple and efficient,which has potential application to synthesis of bis(cyclopentadienone)s.The course of oxidation has been confirmed by isolated intermediates.  相似文献   
55.
An organic hydrogel as a matrix for the growth of calcite crystals   总被引:1,自引:0,他引:1  
The growth of calcite in an aqueous gel of was studied and the appearance of the crystals was found to change over time. Crystals removed from the gel at progressively longer times showed severely affected surfaces resulting from dissolution. If crystals were removed from the gel after 3.5 hours, at which point there were no etch pits, and then placed in either buffer or pure water, etch pits, similar to those observed on crystals that are left in the gel, were observed. Control calcite crystals exposed to similar conditions (water or buffer) show no significant dissolution after equivalent times. A probable cause of the altered dissolution is the non-specific occlusion of gelator aggregates at sites of imperfection. The gel appears to provide a microenvironment in which the molecules that form the matrix also participate in the crystallization. This system allows the study of the unique properties of a gel for influencing the nucleation and growth of inorganic crystals, some of which may be important for better understanding biomineralization.  相似文献   
56.
本文通过单晶X-射线衍射法测定了EtEDTB1.4C2H5OH5H2O 1和H4EtEDTB(ClO4)4 C2H5OH 2的晶体结构。晶体学数据如下:1的分子式为C44.8H66.4N10O6.4, Mr = 847.48, 属三斜晶系, 空间群P, a = 11.489 (2), b = 11.866(3), c = 12.002(3) , = 97.47(2), ?= 114.564(13), ?= 114.11(2)? V = 1266.6(5) 3, Z = 1, Dc = 1.111 g/cm3, F(000) = 456, m(MoK? = 0.076 mm-1。共收集衍射数据5207条, 其中独立衍射数据4323条(Rint = 0.0257), 1318条可观测衍射数据(I > 2(I))用于结构计算。结构由直接法解出, 并用全矩阵最小二乘法修正, 最终偏离因子R = 0.0706, wR = 0.1802。分子具有对称中心, 4个苯并咪唑基团围绕中心呈螺旋桨状均匀排布。在1的晶体中, EtEDTB分子通过水和乙醇的氢键相连形成二维网状结构。2的分子式为C44H58Cl4N10O17, Mr = 1140.80, 属单斜晶系, 空间群C2/c, a = 24.260(5), b = 13.040(3), c = 17.680(4) , ?= 97.50(3)? V = 5545.2(2) 3, Z = 4, Dc = 1.366 g/cm3, F(000) = 2384, m(MoK? = 0.289 mm-1。共收集衍射数据12055条, 其中独立衍射数据6360条(Rint = 0.0408), 2875条可观测衍射数据(I > 2(I))用于结构计算。结构由直接法解出, 并用全矩阵最小二乘法修正, 最终偏离因子R = 0.0692  相似文献   
57.
A regio-and stereo-selective synthesis of multi-substituted 3-pyrrolines has been developed.The multi-substituted 3-pyrrolines were synthesized in good yields by 1,3-dipolar cycloaddition of methyl 2-(phenylselanyl)acrylate with azomethine ylides,followed by N-acylation and oxidation-elimination of phenylseleno group.  相似文献   
58.
A sensitive approach for the qualitative detection of DNA-binding protein on the microarray was developed.DNA complexes in which a partial duplex region is formed from a biotin-primer and a circle single strand DNA(ssDNA) were spotted on a microarray. The endonuclease recognition site(ERS) and the DNA-binding sites(DBS) were arranged side by side within the duplex region. The working principle of the detection system is described as follows:when the DNA-binding protein capture the DBS,the endonuclease co...  相似文献   
59.
The reaction of Os~+(~6D,~4F) with N_2O has been investigated at B3LYP/TZVP and CCSD(T)/6-311+G~* levels of theory.The mechanisms corresponding to O-atom and N-atom transfer reactions have been revealed.It was found that on the sextet reaction surface both the O-atom and N-atom transfer reactions undergo through direct-abstraction mechanism,leading to the formation of OsO~+ and OsN~+,whereas on quartet surface the two reactions undergo through O-N bond or N-N bond insertion mechanism.The calculated energ...  相似文献   
60.
Monoclonal antibodies were selected after immunization with crystals of the tripeptide l-leucine-l-leucine-l-tyrosine. They interact with the tripeptide crystals, but do not interact with the tripeptide molecule, with other crystalline surfaces, or with adsorbed protein. The interactions of two antibodies with crystals of l-Leu-l-Leu-l-Tyr and of its enantiomer d-Leu-d-Leu-d-Tyr were characterized in depth. Antibody 48E is stereoselective and enantioselective: it recognizes only the [011] faces of the l-Leu-l-Leu-l-Tyr crystals, and not the enantiomorphous [011] faces of d-Leu-d-Leu-d-Tyr crystals, or any other faces of either crystal. In contrast, antibody 602E is poorly stereoselective and is not enantioselective: it recognizes the crystals of both enantiomers, interacting with a number of different faces of each. The different recognition patterns are explained on the basis of the nature of the interactions and the structure of the interacting surfaces. Understanding this antibody specificity advances our general understanding of surface recognition and transfer of chiral information across biological interfaces.  相似文献   
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