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71.
Nina Lah Gregor Rep Primo egedin Ljubo Goli
Ivan Leban 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(6):642-643
The structure of the title compound, Na2[Zn(C6H11O2)4], consists of two‐dimensional polymeric sheets. The Zn2+ ions are approximately tetrahedrally coordinated by O atoms from different hexanoate anions. Both Na+ ions are six‐coordinated by carboxylate O atoms. One of the hexanoate O atoms is attached to one Zn2+ ion and one Na+ ion, and the remaining O atom is attached to two Na+ ions. 相似文献
72.
73.
Nader M. Boshta Martin Bomkamp Gregor Schnakenburg Dr. Siegfried R. Waldvogel Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(11):3459-3466
The oxidative trimerization of catechol ketals by MoCl5 or MoCl5/TiCl4 mixtures leads preferentially to the all‐syn stereoisomer of the corresponding triphenylene ketal. The concomitant metal salts of the oxidative coupling most probably form a multinuclear template that directs the diastereoselectivity in a subsequent isomerization step under electrophilic conditions. Several functionalities can serve as coordination sites for the multinuclear metal chloro clusters. Suitable functional groups have to be stable towards the strong electrophilic and oxidizing conditions. Therefore, esters, nitriles, nitro derivatives, triazoles, and pyridines are successfully employed. Based on the flexibility and size of the substrate, different reagent mixtures lead to the stereoselective formation of the all‐syn derivatives. 相似文献
74.
75.
Dinar Abdullin Nicole Florin Dr. Gregor Hagelueken Prof. Dr. Olav Schiemann 《Angewandte Chemie (International ed. in English)》2015,54(6):1827-1831
Metal ions play an important role in the catalysis and folding of proteins and oligonucleotides. Their localization within the three‐dimensional fold of such biomolecules is therefore an important goal in understanding structure–function relationships. A trilateration approach for the localization of metal ions by means of long‐range distance measurements based on electron paramagnetic resonance (EPR) is introduced. The approach is tested on the Cu2+ center of azurin, and factors affecting the precision of the method are discussed. 相似文献
76.
Romana Cerc Korošec Silvija Renko Gregor Rep Peter Bukovec 《Journal of Thermal Analysis and Calorimetry》2017,130(3):1383-1390
Thermal modification is one of the environmental friendly wood preservation technologies. During this process, changes of the main woody cell wall components occur, which lead to improved dimensional stability, lower hygroscopicity and improvement in biological durability. Several chemical reactions which occur during thermal treatment of wood caused changes in wood properties. During TG measurements, thermal decomposition reactions, which was not completed during previous thermal modification process, continued in wood samples, meaning that more thermally treated samples exhibited lower mass losses in a certain or whole temperature range up to 600 °C. Therefore, mass loss, obtained within selected temperature range, could be used as a marker of previous thermal treatment. The aim of the present work is to evaluate suitability of a thermogravimetric method (TG) for determination of a degree of thermal treatment of beech wood. On the basis of thermally untreated sample and those which were thermally modified at 180, 190, 200, 210, 215 and 220 °C in the absence of oxygen, respectively, and with known values of mass loss during the modification processes, several calibration curves were constructed. They represent mass loss in a certain temperature range during TG measurement versus mass loss during previous thermal modification. In a temperature range from 130 to 300 °C and from 130 to 320 °C under nitrogen atmosphere, a linear dependence was observed; correlation coefficients R 2 were 0.87 and 0.91, respectively. In wider temperature range and under air atmosphere, lower correlation coefficients were obtained. High correlation coefficient, higher than 0.95, was observed in a temperature range from 25 to 130 °C under both atmospheres. In this region, dehydration due to rehydration of thermally modified samples occurs. The results of this work were compared with those obtained for Norway spruce. 相似文献
77.
Schmidt C Götzen J Witte G 《Langmuir : the ACS journal of surfaces and colloids》2011,27(3):1025-1032
The structure and thermal stability of self-assembled monolayers (SAMs) of benzenethiolate (BT) on Cu(100) have been studied by means of thermal desorption spectroscopy (TDS), scanning tunneling microscopy (STM), low-energy electron diffraction (LEED), UV photoelectron spectroscopy (UPS), X-ray photoelectron spectroscopy (XPS), and near-edge X-ray adsorption fine structure spectroscopy (NEXAFS). Vapor deposition at room temperature yields a well-ordered, densely packed c(6 × 2) saturation structure. At room temperature, this film is, however, metastable and transforms via partial decomposition by cleavage of the S-C bond into a less densely packed layer that reveals a coexisting p(2 × 2) phase. Such a transition occurs on a time scale of several days and is accompanied by a reduction of the work function change with respect to the bare Cu(100) surface from Δ? = -0.9 eV for a freshly prepared saturated layer to -0.5 eV for an aged film. TDS experiments exhibit the presence of two distinct desorption channels (dissociative and intact desorption) occurring at different temperatures that reflects a variation of the local Cu-S interaction strength of BT at differently coordinated adsorption sites. Heating to above room temperature causes a rapid degradation and continuous thinning of BT films whereas above 500 K all thiolate species have desorbed or dissociated, leaving a sulfide overlayer behind that is accompanied by a substrate reconstruction. Interestingly, the upright orientation of BT adopted in the saturated monolayer remains almost identical upon heating and demonstrates the absence of downward tilting upon thermally induced thinning of the film. 相似文献
78.
Albrecht C Bode M Pérez JM Daniels J Schnakenburg G Streubel R 《Dalton transactions (Cambridge, England : 2003)》2011,40(11):2654-2665
Synthesis of the first oxaphosphirane chromium(0) and molybdenum(0) complexes of the type [{(R(1)PCH(R(2))-O}M(CO)(5)] (R(1) = C(5)Me(5)) (8a-e, 15a-e) and (R(1) = CH(SiMe(3))(2)) (9a-e, 16a-e) via reaction of dichloro(organo)- (1, 2, 10, 11) and chloro(organo)phosphane complexes (3,4,12) with lithium bases and aldehydes 7a-e is reported. Furthermore, bicyclic 1,3-oxaphospholane complexes 17 and 18 have been obtained via O-protonation of oxaphosphirane complexes 8a and 15a with HCl. All complexes were characterized by NMR, IR spectroscopic, mass spectrometric investigations and, in addition, single-crystal X-ray structures of complexes 8a-e, 9a,c, 15a,b,e, 16a-c, 17, 18 are presented and discussed. 相似文献
79.
Bechstein K Michels J Vogt J Schwartze GC Vogt C 《Analytical and bioanalytical chemistry》2011,399(1):501-508
Previous studies have revealed silica formation in the teeth of mandibular gnathobases of copepods while significant amounts
of zinc and copper are present, which might improve mechanical stability of the teeth and represent an adaptation to compact
food particles. The present study aimed at analysing the distribution and concentration of trace elements in the mandibular
gnathobases of females of the Antarctic copepod species Calanoides acutus. Because of the low overall masses of few micrograms per specimen the application of a combination of position-resolved micro-beam
techniques was necessary and micro-particle-induced X-ray emission spectrometry and laser ablation inductively coupled plasma
mass spectrometry were used to determine Ba, Br, Ca, Cl, Cu, Fe, K, Mg, Na, Ni, P, S, Si and Zn in the samples with μm to
sub-μm resolution. Calibration strategies were optimised to fit for the carbonate matrix. The analyses revealed a distinct
enrichment of Br, Ca, Fe, K, S, Si and Zn in the teeth of the gnathobases. 相似文献
80.
André Kündgen Gregor LeanderCarsten Thomassen 《Journal of Combinatorial Theory, Series A》2011,118(7):2025-2034
A directed graph is called central if its adjacency matrix A satisfies the equation A2=J, where J is the matrix with a 1 in each entry. It has been conjectured that every central directed graph can be obtained from a standard example by a sequence of simple operations called switchings, and also that it can be obtained from a smaller one by an extension. We disprove these conjectures and present a general extension result which, in particular, shows that each counterexample extends to an infinite family. 相似文献