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971.
Diaryliodonium salts are demonstrated as efficient arylating agents of aliphatic alcohols under metal-free conditions. The reaction proceeds at room temperature within 90 min to give alkyl aryl ethers in good to excellent yields. Aryl groups with electron-withdrawing substituents are transferred most efficiently, and unsymmetric iodonium salts give chemoselective arylations. The methodology has been applied to the formal synthesis of butoxycaine. 相似文献
972.
Computational Insight into Nickel‐Catalyzed Carbon–Carbon versus Carbon–Boron Coupling Reactions of Primary,Secondary, and Tertiary Alkyl Bromides
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Dr. Man Sing Cheung Fu Kit Sheong Prof. Dr. Todd B. Marder Prof. Dr. Zhenyang Lin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(20):7480-7488
The nickel‐catalyzed alkyl–alkyl cross‐coupling (C?C bond formation) and borylation (C?B bond formation) of unactivated alkyl halides reported in the literature show completely opposite reactivity orders in the reactions of primary, secondary, and tertiary alkyl bromides. The proposed NiI/NiIII catalytic cycles for these two types of bond‐formation reactions were studied computationally by means of DFT calculations at the B3LYP level. These calculations indicate that the rate‐determining step for alkyl–alkyl cross‐coupling is the reductive elimination step, whereas for borylation the rate is determined mainly by the atom‐transfer step. In borylation reactions, the boryl ligand involved has an empty p orbital, which strongly facilitates the reductive elimination step. The inability of unactivated tertiary alkyl halides to undergo alkyl–alkyl cross‐coupling is mainly due to the moderately high reductive elimination barrier. 相似文献
973.
Naphthalene‐Functionalized,Photoluminescent Room Temperature Ionic Liquids Bearing Small Counterions
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Hongxia Zhu Geping Zhang Mengjun Chen Shengju Zhou Guihua Li Xiaolin Wang Prof. Qingzeng Zhu Prof. Hongguang Li Prof. Jingcheng Hao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(18):6286-6293
Obtaining π‐conjugated room temperature ionic liquids (RTILs) is difficult because of the relatively strong π–π interaction among the π‐moieties. Existing strategies by using bulky counterions greatly hindered further property optimization and potential applications of these intriguing functional fluids through simple ion exchange. Herein, four naphthalene‐functionalized, π‐conjugated RTILs with small counterions (Br?) have been facilely synthesized with high yields. Our strategy is to attach branched alkyl chains to the cationic backbone of the target compounds ( 2 a – d ), which effectively tune inter‐ and intramolecular interactions. Compounds 2 a – d have satisfactory thermal stability (up to 300 °C) and low melting points (<?19 °C). Rheological measurements revealed the fluid character of 2 a – d , whose viscosity decrease with the increase of the alkyl chain length and temperature. The presence of the π‐conjugated naphthalene moiety imparts 2 a – d photoluminescent properties in bulk solutions. Moreover, the absence of strong π–π stacking among the naphthalene units in solvent‐free states enables them to be used as a new generation of photoluminescent inks. 相似文献
974.
Synthesis and characterization of chiral poly(l‐lactide‐b‐hexyl isocyanate) macromonomers with norbornenyl end groups and their homopolymerization through ring opening metathesis polymerization to afford polymer brushes
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Ioannis Choinopoulos Spyros Koinis Marinos Pitsikalis 《Journal of polymer science. Part A, Polymer chemistry》2017,55(6):1102-1112
We report the synthesis of the novel half‐titanocene alkoxide complex bischloro‐η5‐cyclopentadienyl(bicyclo[2.2.1]‐hept‐5‐en‐2‐oxy) titanium (IV), [CpTiCl2(O‐NBE)]. This complex was employed for the synthesis of chiral poly(l ‐lactide‐b‐hexyl isocyanate) diblock copolymer bearing a norbornene end group with sequential addition of monomers. The poly(hexyl isocyanate) block is chiral due to the last l ‐lactide unit of the poly(l ‐lactide) block. This macromonomer was polymerized towards a chiral polymer brush structure with polynorbornene backbone and chiral poly(l ‐lactide‐b‐hexyl isocyanate) side chains using Grubbs first‐generation catalyst. The polymers were characterized using size exclusion chromatography (SEC), nuclear magnetic resonance (NMR), and circular dichroism (CD) spectroscopy and their thermal properties were investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) analysis. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 1102–1112 相似文献
975.
Intermolecular Photocatalyzed Heck‐like Coupling of Unactivated Alkyl Bromides by a Dinuclear Gold Complex
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Dr. Jin Xie Dr. Jian Li M. Sc. Vanessa Weingand Dr. Matthias Rudolph Prof. Dr. A. Stephen K. Hashmi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(36):12646-12650
A practical protocol for a photocatalyzed alkyl‐Heck‐like reaction of unactivated alkyl bromides and different alkenes promoted by dinuclear gold photoredox catalysis in the presence of an inorganic base is reported. Primary, secondary, and tertiary unactivated alkyl bromides with β‐hydrogen can be applied. Esters, aldehydes, ketones, nitriles, alcohols, heterocycles, alkynes, alkenes, ethers, and halogen moieties are all well tolerated. In addition to 1,1‐diarylalkenes, silylenolethers and enamides can also be applied, which further increases the synthetic potential of the reaction. The mild reaction conditions, broad substrate scope, and an excellent functional‐group tolerance deliver an ideal tool for synthetic chemists that can even be used for challenging late‐stage modifications of complex natural products. 相似文献
976.
Sang Hwi LeeIn Su Kim Qing Ri LiGuang Ri Dong Young Hoon Jung 《Tetrahedron letters》2011,52(16):1901-1904
The introduction of amines to allylic or benzylic position of cyclic compounds with chlorosulfonyl isocyanate is developed in high to excellent yields. This method provides a novel access to biologically active compounds including the framework of 1-aminoindanes, 1-aminotetralines, and 1-amino-2-hydroxy cyclic compounds. Mechanistic evidence for the reaction pathway is also provided. 相似文献
977.
Burcin Akgun Emre Savci Duygu Avci 《Journal of polymer science. Part A, Polymer chemistry》2012,50(4):801-810
Novel phosphonate and phosphonic acid‐containing bis(methacrylamide)s were synthesized. The phosphonate‐containing monomers ( 1a and 1b ) were synthesized by amidation of 2‐(2‐chlorocarbonyl‐allyloxymethyl)‐acryloylchloride with diethyl 2‐aminoethylphosphonate and diethyl 1‐aminomethylphosphonate. The phosphonic acid‐containing monomers ( 2a and 2b ) were synthesized by hydrolysis of 1a and 1b with trimethylsilyl bromide (TMSBr). All monomers were liquids and dissolved in water and ethanol. Thermal homopolymerization of 1a and 1b in bulk and solution using 2,2′‐azobis(isobutyronitrile) (AIBN) at 80 °C gave crosslinked polymers indicating low cyclization tendencies of these monomers. They were also homopolymerized using photo‐DSC with 2,2′‐dimethoxy‐2‐phenyl acetophenone (DMPA) as photoinitator, and their maximum rates of polymerization were found to be higher than commercial monomers 2,2‐bis[4‐(2‐hydroxy‐3‐methacryloyloxy propyloxy) phenyl] propane (Bis‐GMA) and 2‐hydroxyethyl methacrylate (HEMA), indicating their potential as reactive diluents or crosslinkers in dental materials. In fact, copolymerization with monomer 1a resulted in improvements in photopolymerization kinetics of both Bis‐GMA and HEMA. The acidic nature of the aqueous solutions (pH of 2a : 1.42, 2b : 1.53), stability under aqueous conditions after 1 month of study at 37 °C, interaction of 2a with hydroxyapatite (HAP) as representative of both monomers, and copolymerizability of the same with HEMA make these monomers suitable as adhesive monomers in dental adhesives, although their low observed reactivities may present a drawback. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
978.
979.
Assem O. Barakat Susan Baumgart Peter Brocks Barbara M. Scholz‐Böttcher Jürgen Rullkötter 《Journal of mass spectrometry : JMS》2012,47(8):987-994
Several series of alkylated phenols were detected for the first time in the extractable bitumens of organic matter‐rich sediments from the Nördlinger Ries (southern Germany). Most abundant and significant constituents comprise those with n‐octadecyl, n‐eicosanyl, phytanyl, and iso‐pentadecyl and anteiso‐pentadecyl substituents. The structures of these compounds are suggested from mass spectrometric and retention time data and coinjection with synthetic standards. Diagenetic alteration of phenolic algal lipids is suggested as a possible way to the formation of these compounds in the Nördlinger Ries sediments. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
980.
Three primary nerve agent degradation products (ethyl-, isopropyl- and pinacolyl methylphosphonic acid) have been determined in water samples using on-line solid phase extraction-liquid chromatography and mass spectrometry (SPE-LC–MS) with electrospray ionisation. Porous graphitic carbon was employed for analyte enrichment followed by hydrophilic interaction chromatography. Diethylphosphate was applied as internal standard for quantitative determination of the alkyl methylphosphonic acids (AMPAs). By treating the samples with strong cation-exhange columns on Ba, Ag and H form, the major inorganic anions in water were removed by precipitation prior to the SPE-LC–MS determination. The AMPAs could be determined in tap water with limits of detection of 0.01–0.07 μg L−1 with the [M−H]− ions extracted at an accuracy of ±5 mDa. The within and between assay precisions at analyte concentrations of 5 μg L−1 were 2–3%, and 5–9% relative standard deviation, respectively. The developed method was employed for determination of the AMPAs in three natural waters and a simulated waste water sample, spiked at 5 μg L−1. Recoveries of ethyl-, isopropyl- and pinacolyl methylphosphonic acid were 80–91%, 92–103% and 99–106%, respectively, proving the applicability of the technique for natural waters of various origins. 相似文献