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101.
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Phosphonate reagents were developed for the two-carbon homologation of aldehydes or ketones to unbranched- or methyl-branched α,β-unsaturated aldehydes. The phosphonate reagents, diethyl methylformyl-2-phosphonate dimethylhydrazone and diethyl ethylformyl-2-phosphonate dimethylhydrazone, contained a protected aldehyde group instead of the usual ester group. A homologation cycle entailed condensation of the reagent with the starting aldehyde, followed by removal of the dimethylhydrazone protective group with a biphasic mixture of 1 M HCl and petroleum ether. This robust two-step process worked with a variety of aldehydes and ketones. Overall isolated yields of unsaturated aldehyde products ranged from 71% to 86% after the condensation and deprotection steps. 相似文献
103.
Dual functions of a novel low-gap polymer for near infra-red photovoltaics and light-emitting diodes
Li P Fenwick O Yilmaz S Breusov D Caruana DJ Allard S Scherf U Cacialli F 《Chemical communications (Cambridge, England)》2011,47(31):8820-8822
We have synthesised and characterised a new low-gap conjugated polymer, with a broad absorption profile. In blends with a C(70) derivative we demonstrate power conversion efficiencies of 0.76%. We show electroluminescence from the polymer peaking at 956 nm, and quantum efficiency of 0.02% in a blend. 相似文献
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Krystyna Baczko Hélène Fensterbank Bruno Berini Nadège Bordage Gilles Clavier Rachel Méallet‐Renault Chantal Larpent Emmanuel Allard 《Journal of polymer science. Part A, Polymer chemistry》2016,54(1):115-126
This work deals with the covalent coupling of azide‐functionalized polymeric nanoparticles as a reactive core and amino‐terminated PAMAM dendrons as a reactive shell. The nanoassemblies thereby obtained could be modified after the dendronization step by grafting an alkynyl Bodipy dye on the unreacted azide moieties. Only a few steps are required to attain nanoassemblies that could mimic dendrimers of high generation with sizes of nano‐objects beyond those of dendrimers. The structure of the nanoassemblies are composed of a polystyrene core, an inner shell including the Bodipy dyes along with the internal branches of the PAMAM, and the terminal amino groups from the outer shell. The dendritic shell acts as a protective layer that prevents NP from aggregation in a surfactant free aqueous solution. The nano‐objects display absorption and emission maxima above 500 nm with brightness that are the same order of magnitude than Qdots. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 115–126 相似文献
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Dr. Eugénie Fournier Dr. Sybille Tachon Dr. Nicholas J. Fowler Dr. Guillaume Gerbaud Dr. Pascal Mansuelle Dr. Pierre Dorlet Dr. Sam P. de Visser Prof. Valérie Belle Dr. A. Jalila Simaan Dr. Marlène Martinho 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(60):13766-13776
1-Aminocyclopropane-1-carboxylic oxidase (ACCO) is a non-heme iron(II)-containing enzyme involved in the biosynthesis of the phytohormone ethylene, which regulates fruit ripening and flowering in plants. The active conformation of ACCO, and in particular that of the C-terminal part, remains unclear and open and closed conformations have been proposed. In this work, a combined experimental and computational study to understand the conformation and dynamics of the C-terminal part is reported. Site-directed spin-labeling coupled to electron paramagnetic resonance (SDSL-EPR) spectroscopy was used. Mutagenesis experiments were performed to generate active enzymes bearing two paramagnetic labels (nitroxide radicals) anchored on cysteine residues, one in the main core and one in the C-terminal part. Inter-spin distance distributions were measured by pulsed EPR spectroscopy and compared with the results of molecular dynamics simulations. The results reveal the existence of a flexibility of the C-terminal part. This flexibility generates several conformations of the C-terminal part of ACCO that correspond neither to the existing crystal structures nor to the modelled structures. This highly dynamic region of ACCO raises questions on its exact function during enzymatic activity. 相似文献
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Martin Simoneau Pierre Mercier Jean Blouin Paul Allard Normand Teasdale 《BMC neuroscience》2006,7(1):68-9