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Debojyoti Bag Prof. Sanghapal D. Sawant 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(4):1165-1218
Heteroarene-tethered functionalized alkynes are multipotent synthons in organic chemistry. This detailed Review described herein offers a thorough discussion of the metamorphosis of heteroarene-tethered functionalized alkynes, an area which has earned much attention over the past decade in the straightforward synthesis of architecturally complex heterocyclic scaffolds in atom and step economic manner. Depending upon the variety of functionalized alkynes, this Review is divided into multiple sections. Amongst the vast array of synthetic transformations covered, dearomatizing spirocyclizations and cascade spirocyclization/rearrangement are of great interest. Synthetic transformations involving the heteroarene-tethered functionalized alkynes with scope, challenges, limitations, mechanism, their application in the total synthesis of natural products and future perceptions are surveyed. 相似文献
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Synthesis and characterization of a Ni nanoparticle stabilized on Ionic liquid‐functionalized magnetic Silica nanoparticles for tandem oxidative reaction of primary alcohols 下载免费PDF全文
Rahim Hosseinzadeh‐Khanmiri Yaser Kamel Zahra Keshvari Ahmad Mobaraki Gholam Hossein Shahverdizadeh Esmail Vessally Mirzaagha Babazadeh 《应用有机金属化学》2018,32(9)
In this research, preparation of the magnetic nanoparticle, coating by a silica shell using (3‐aminopropyl) triethoxysilane and synthesis of a novel sulfonic acid‐substituted imidazolium‐based ionic liquid onto the surface of these particles via a multi‐component reaction, is described. The functionalized nanoparticles was loaded by Ni nanoparticles and characterized by means of techniques such as XRD, FTIR, SEM, EDX, TEM, TGA and ICP‐OES. The nanostructures have spherical shapes that ranged in size from 80 to 100 nm. The catalytic activity of these nanoparticles was tested in aerobic oxidation of primary alcohols that showed good performance in the wide range of primary alcohols in water at mild reaction conditions. As a second step of this work, the tandem oxidative synthesis of alkylacrylonitriles and bisindolylmethanes were investigated using primary alcohols under oxidation conditions. This catalyst system can be recovered using external magnet and reused for five consecutive cycles without significantly less of its activity. 相似文献
94.
Enolesters as chain end-functionalizing agents for the living ring opening metathesis polymerization
Peng Liu Mohammad Yasir Helena Kurzen Nils Hanik Mark Schäfer Andreas F. M. Kilbinger 《Journal of polymer science. Part A, Polymer chemistry》2017,55(18):2983-2990
Functional enolethers have previously been used to introduce functional end groups at the chain end of ruthenium carbene complex initiated living ring opening metathesis polymers. Here, we investigated whether the weaker π-donating enolesters could equally be used in regio selective reactions with ruthenium carbene complexes and thus as polymer end-functionalization reagents. Enolesters such as vinyl acetate, butenyl acetate, 3-(4-(tert-butoxy)phenyl)propenyl acetate and 6-(((benzyloxy)carbonyl)amino)hex-1-en-1-yl acetate were used as living ROMP terminating agents. All gave the expected end groups proving that enolesters are synthetically easily accessible targets for living ROMP end-functionalization. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2983–2990 相似文献
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Nino Zavradashvili Giuli Jokhadze Marekh Gverdtsiteli Giuli Otinashvili Nino Kupatadze Zaza Gomurashvili 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(5):449-465
A new class of biodegradable functional polymers – epoxy-poly(ester amide)s (EPEAs), was synthesized for the first time on the basis of naturally occurring α-amino acids, fatty diols and cis- and trans-epoxysuccinic acids. The syntheses were conducted via both solution Active Polycondensation and Interfacial Polycondensation using, accordingly, either activated di-p-nitrophenyl esters or dichlorides of cis- and trans-epoxysuccinic acids as bis-electrophilic monomers. Di-p-toluenesulfonic acid salts of bis-(L-phenylalanine)-1,6-hexylene and bis-(L-leucine)-1,6-hexylene diesters were used in both cases as bis-nucleophilic counter-partners. High-molecular-weight polymers (Mw up to 67.000) with desirable material properties were obtained via solution polycondensation using di-p-nitrophenyl-trans-epoxy succinate. The EPEAs were chemically modified further under mild conditions: oxirane groups along the backbone were reacted with both nucleophilic and electrophilic reagents, and also subjected to thermal and chemical curing. The macromolecular transformations of EPEAs substantially broaden material properties and, hence, the potential to apply amino acid-based biodegradable poly(ester amide)s as absorbable drug carriers and surgical devices. 相似文献
96.
The 2H NMR of uniaxially strained swollen chloroprene rubbers and butadiene-styrene copolymers with different crosslink densities is studied. the relative number of chain segments between cross-links of various samples is obtained. the results are in approximate agreement with those obtained from the Flory equilibrium-swelling method. It is found that the enhancement factor G depends not only on the lattice-walk model and swelling of rubber, such as Tanaka etc. expected, but also on the crosslink density and the structure of the rubber. the formula relating G to the number of chain segments between cross links is derived from theory. Moreover, we can also estimate the relation between the enhancement factor Gr of real rubber and G calculated from the theory of the lattice model. the 2H NMR results of these samples indicate that the interaction between chain segments decreases with increasing crosslink density. 相似文献
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Dr. Pablo A. Denis 《Chemphyschem》2013,14(14):3271-3277
Dispersion‐corrected density functional theory is utilized to study the addition of aryl radicals to perfect and defective graphene. Although the perfect sheet shows a low reactivity against aryl diazonium salts, the agglomeration of these groups and the addition onto defect sites improves the feasibility of the reaction by increasing binding energies per aryl group up to 27 kcal mol?1. It is found that if a single phenyl radical interacts with graphene, the covalent and noncovalent additions have similar binding energies, but in the particular case of the nitrophenyl group, the adsorption is stronger than the chemisorption. The single vacancy shows the largest reactivity, increasing the binding energy per aryl group by about 80 kcal mol?1. The zigzag edge ranks second, enhancing the reactivity 5.4 times with respect to the perfect sheet. The less reactive defect site is the Stone–Wales type, but even in this case the addition of an isolated aryl radical is exergonic. The arylation process is favored if the groups are attached nearby and on different sublattices. This is particularly true for the ortho and para positions. However, the enhancement of the binding energies decreases quickly if the distance between the two aryl radicals is increased, thereby making the addition on the perfect sheet difficult. A bandgap of 1–2 eV can be opened on functionalization of the graphene sheets with aryl radicals, but for certain configurations the sheet can maintain its semimetallic character even if there is one aryl radical per eight carbon atoms. At the highest level of functionalization achieved, that is, one aryl group per five carbon atoms, the bandgap is 1.9 eV. Regarding the effect of using aryl groups with different substituents, it is found that they all induce the same bandgap and thus the presence of NO2, H, or Br is not relevant for the alteration of the electronic properties. Finally, it is observed that the presence of tetrafluoroborate can induce metallic character in graphene. 相似文献
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