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Sensing of Phosphates by Using Luminescent EuIII and TbIII Complexes: Application to the Microalgal Cell Chlorella vulgaris 下载免费PDF全文
Sandeep Nadella Jashobanta Sahoo Dr. Palani S. Subramanian Abhishek Sahu Dr. Sandhya Mishra Prof. Dr. Markus Albrecht 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(20):6047-6053
Phenanthroline‐based chiral ligands L1 and L2 as well as the corresponding EuIII and TbIII complexes were synthesized and characterized. The coordination compounds show red and green emission, which was explored for the sensing of a series of anions such as F?, Cl?, Br?, I?, NO3?, NO2?, HPO42?, HSO4?, CH3COO?, and HCO3?. Among the anions, HPO42? exhibited a strong response in the emission property of both europium(III) and terbium(III) complexes. The complexes showed interactions with the nucleoside phosphates adenosine triphosphate (ATP), adenosine diphosphate (ADP), and adenosine monophosphate (AMP). Owing to this recognition, these complexes have been applied as staining agents in the microalgal cell Chlorella vulgaris. The stained microalgal cells were monitored through fluorescence microscopy and scanning electron microscopy. Initially, the complexes bind to the outer cell wall and then enter the cell wall through holes in which they probably bind to phospholipids. This leads to a quenching of the luminescence properties. 相似文献
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Designed transition metal complexes predominantly catalyze Michael addition reactions. Inorganic and organic base‐catalyzed Michael addition reactions have been reported. However, known base‐catalyzed reactions suffer from the requirement of solvents, additives, high pressure and also side‐reactions. Herein, we demonstrate a mild and environmentally friendly strategy of readily available KOtBu‐catalyzed Michael addition reactions. This simple inorganic base efficiently catalyzes the Michael addition of underexplored acrylonitriles, esters and amides with (oxa‐, aza‐, and thia‐) heteroatom nucleophiles. This catalytic process proceeds under solvent‐free conditions and at room temperature. Notably, this protocol offers an easy operational procedure, broad substrate scope with excellent selectivity, reaction scalability and excellent TON (>9900). Preliminary mechanistic studies revealed that the reaction follows an ionic mechanism. Formal synthesis of promazine is demonstrated using this catalytic protocol. 相似文献
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Pratap V Moumen N Subramanian RS 《Langmuir : the ACS journal of surfaces and colloids》2008,24(9):5185-5193
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Singh L Ishar MP Elango M Subramanian V Gupta V Kanwal P 《The Journal of organic chemistry》2008,73(6):2224-2233
Thermal and microwave assisted [4+2] cycloadditions of 1,4-diaryl-1-aza-1,3-butadienes with allenic esters lead to cycloadducts, which after a 1,3-H shift afford variedly substituted unsymmetrical 2-alkyl-1,4-diaryl-3-ethoxycarbonyl-1,4-dihydropyridines in high yields. Reactions carried out under microwave irradiation are cleaner and give higher yields with much shortened reaction times. Density functional theory (DFT) at the B3LYP/6-31G* level has been used to calculate geometric features of the reactants, barrier for s-trans to s-cis and reverse isomerization of azadienes (5a-d, 10a-e), dihedral angles between N(1), C(2), C(3), and C(4) atoms of azadienes along with various indices such as chemical hardness (eta), chemical potential (micro), global electrophilicity (omega), and the difference in global electrophilicity (Deltaomega) between the reacting pairs and Fukui functions (f (+) and f(-)). The results revealed that s-trans is the predominant conformation of azadienes at ambient temperature and the barrier for conversion of the s-trans rotamer of 1-azadienes to s-cis may be the major factor influencing the chemoselectivity, i.e., [4+2] verses [2+2] cycloaddition. The regiochemistry of the observed cycloadditions is collated with the obtained local electrophilicity indices (Fukui functions). Transition states for the formation of both [4+2] and [2+2] cycloadducts as located at the PM3 level indicate that the transition state for the formation of [4+2] cycloadducts has lower energy, again supporting the earlier conclusion that preferred formation of [4+2] cycloaaducts at higher temperature may be a consequence of barrier for s-trans to s-cis transformation of 1-azadienes. 相似文献
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R. K. Itawi S. Subramanian Z. R. Turel 《Journal of Radioanalytical and Nuclear Chemistry》1990,138(1):63-66
The toxicity of Se, Cd, and Hg as environmental pollutants and the impact of these elements on the aquatic ecosystem is undisputed. The present paper reports an investigation of the concentration of Cd, Se, and Hg in an aquatic environment of a large metropolitan city like Bombay. As the toxicity of these elements manifests itself at micro and submicro levels, the very sensitive technique of neutron activation analysis was employed. A sequential substoichiometric extraction technique for the separation of radiochemically pure203Hg,75Se, and115–115mCd from the neutron irradiated target has also been employed. 相似文献
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