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81.
Dotsenko V. V. Krivokolysko S. G. Chernega A. N. Litvinov V. P. 《Russian Chemical Bulletin》2003,52(4):969-977
The reactions of N-methylmorpholinium 4-aryl(hetaryl)-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates with malononitrile and acetone in ethanol afforded substituted tetrahydropyridothienopyridinones. In the absence of acetone, tetrahydropyridothiopyranopyridinones were isolated as the major reaction products. The latter were also synthesized independently by the reactions of the above-mentioned thiolates with 2-amino-1,1,3-tricyanopropene. The structure of 2,4-diamino-10-(2-chlorophenyl)-3-cyano-5-imino-8-oxo-7,8,9,10-tetrahydro-5H-pyrido[2",3":2,3]thiopyrano[4,5-b]pyridine was established by X-ray diffraction analysis. 相似文献
82.
Molar heat capacities of the pure samples of acetone,methanol and the azeotropic mixture composed of acetone,cyclohexane and methanol were measured by an adiabatic calorimeter from 78 to 320 K.The solid-solid andsolid-liquid phase transitions of the pure samples and the mixture were determined based on the curve of the heatcapacity with respect to temperature.The phase transitions took place at(126.16±0.68)and(178.96±1.47)K forthe sample of acetone,(157.79±0.95)and(175.93±0.95)K for methanol,which were corresponding to thesolid-solid and the solid-liquid phase transitions of the acetone and the methanol,respectively.And the phase tran-sitions occurred in the temperature ranges of 120 to 190 K and 278 to 280 K corresponding to the solid-solid andthe solid-liquid phase transitions of mixture of acetone,cyclohexane and methanol,respectively.The thermody-namic functions and the excess thermodynamic functions of the mixture relative to standard temperature of 298.15K were derived based on the relationships of the thermodynamic functions and the function of the measured heatcapacity with respect to temperature. 相似文献
83.
Ligandless heterogeneous palladium: an efficient and recyclable catalyst for Suzuki‐type cross‐coupling reaction 下载免费PDF全文
A mild and efficient ligand‐free Suzuki‐type cross‐coupling reaction of benzoyl chlorides and arylboronic acids catalyzed by heterogeneous Pd/C was developed. Benzoyl chlorides undergo cross‐coupling with electronically diverse arylboronic acids to give biaryl ketones in excellent yield, under aqueous media and optimum temperature. The application of 3 mol% of 10 wt% Pd/C to the cross‐coupling delivers utmost efficiency, and could be reused up to many consecutive cycles without any loss in activity. This method proceeds under aqueous media and a recyclable catalytic system, offering an environmentally benign alternative to the existing protocols. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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86.
本文提出了一种气相色谱-傅里叶变换红外光谱联用技术分析工业丙酮杂质成份的方法,该方法采用FFAP毛细管柱,柱长25m,内径0.25mm,膜厚0.33μm,占总面积1.16%的12种杂能够被分离和鉴定。 相似文献
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88.
LU Xiao Ming 《结构化学》2000,(3)
1 INTRODUCTIONPolymolybdateanionshavebeenstudiedformanyyearsbecauseoftheirapplica tionincatalysischemistry〔1〕.Inthesynthesisoforganicpolymolybdatederivativesusingacetoneassolvent,wefoundthatthecondensationreactionofacetoneoccurredandthecondensationprod… 相似文献
89.
Jing Xu Yuhong Ma Jingyi Xie F.J. Xu Wantai Yang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(12):2755-2760
A universal photoassisted pathway to functionalize polymeric surfaces is presented by transferring the inert surface sp3 C? H bonds into reactive groups, such as ? SO3H, ? NH2, ? SH, and ? COOH. The proposed method uses acetone as photoinitiator and different phenols with a para substituent XR as the reactants. Acetone excited by UV irradiation acts as a pair of scissors cutting both the surface C? H bonds of the polymer substrate and the O? H bonds of phenol, leading to the formation of carbon‐centered surface chain free radicals and oxygen‐centered phenoxy free radicals. By coupling of these two radicals, a variety of functional X groups with an R spacer from XR species of different phenol reactants were readily bonded to the polymeric surfaces, where phenol reactants included 4‐hydroxylbenzene sulfonic acid for ? SO3H, p‐aminophenol and tyramine for ? NH2, 4‐hydroxythiophenol for ? SH, and tyrosine for ? COOH. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
90.
Mohamed S. Abu-Bakr Anwar S. El-Shahawy Seddique M. Ahmed 《Journal of solution chemistry》1993,22(7):663-675
The visible absorption spectra of 4-(2-benzothiazolylazo)resorcinol (BTAR) and 4-(2-benzothiazolylazo)salicylic acid (BTAS) have been recorded in water-organic solvent mixtures in the pH range 0.5–12.0. The organic solvents used are methanol, ethanol,n-propanol, iso-propanol, acetone, dioxane and dimethyl formamide. The spectral changes have been explained in terms of shifts in equilibria among different molecular and ionic species of BTAR and BTAS existing in solution. The pK
a
values corresponding to the different ionization steps have been determined at 25°C and I=0.1M (KNO3) by graphic analysis of the absorbance-pH curves. The results obtained are discussed in terms of the molecular structure of the reagents and the nature of the organic co-solvent used. 相似文献