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61.
Govindasamy Chandrasekar 《Journal of Non》2008,354(33):4027-4030
A supernatant solution of silicate species extracted from coal fly ash in a power plant by alkali fusion was used under acidic conditions to prepare a mesoporous silica, SBA-16. SBA-16 was used as a template for the synthesis of a mesoporous carbon using sucrose as a carbon source. These mesoporous silica and carbon materials were characterized by XRD, N2 adsorption-desorption, SEM, and TEM. Textural properties of the silica and carbon samples prepared using fly ash were found to be comparable to those prepared by pure chemicals, successfully demonstrating the feasibility of recycling fly ash for the synthesis of high quality porous materials. 相似文献
62.
Usha G. Karpagalakshmi K. Ramalakshmi S. Prakash R. Lakshminarayanan P. Yang C. Selvapalam N. 《Russian Journal of Organic Chemistry》2021,57(12):1988-1992
Russian Journal of Organic Chemistry - Glycolurils are building blocks for the synthesis of cucurbiturils that are important host materials for several applications. Glycolurils are prepared... 相似文献
63.
The Remarkable Effect of Halogen Substitution on the Membrane Transport of Fluorescent Molecules in Living Cells
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Harinarayana Ungati Dr. Vijayakumar Govindaraj Prof. Dr. Govindasamy Mugesh 《Angewandte Chemie (International ed. in English)》2018,57(29):8989-8993
Small‐molecule‐based fluorescent probes have become important tools in biology for sensing and imaging applications. However, the biological applications of many of the fluorescent molecules are hampered by low cellular uptake and high toxicity. In this paper, we show for the first time that the introduction of halogen atoms enhances the cellular uptake of fluorescent molecules and the nature of halogen atoms plays a crucial role in the plasma membrane transport in mammalian cells. The remarkably higher uptake of iodinated compounds compared to that of their chloro or bromo analogues suggests that the strong halogen bonding ability of iodine atoms may play an important role in the membrane transport. This study provides a novel strategy for the transport of fluorescent molecules across the plasma membrane in living cells. 相似文献
64.
Antioxidant and Prooxidant Nanozymes: From Cellular Redox Regulation to Next-Generation Therapeutics
Dr. Namrata Singh G. R. Sherin Prof. Dr. Govindasamy Mugesh 《Angewandte Chemie (International ed. in English)》2023,62(33):e202301232
Nanozymes, nanomaterials with enzyme-mimicking activity, have attracted tremendous interest in recent years owing to their ability to replace natural enzymes in various biomedical applications, such as biosensing, therapeutics, drug delivery, and bioimaging. In particular, the nanozymes capable of regulating the cellular redox status by mimicking the antioxidant enzymes in mammalian cells are of great therapeutic significance in oxidative-stress-mediated disorders. As the distinction of physiological oxidative stress (oxidative eustress) and pathological oxidative stress (oxidative distress) occurs at a fine borderline, it is a great challenge to design nanozymes that can differentially sense the two extremes in cells, tissues and organs and mediate appropriate redox chemical reactions. In this Review, we summarize the advances in the development of redox-active nanozymes and their biomedical applications. We primarily highlight the therapeutic significance of the antioxidant and prooxidant nanozymes in various disease model systems, such as cancer, neurodegeneration, and cardiovascular diseases. The future perspectives of this emerging area of research and the challenges associated with the biomedical applications of nanozymes are described. 相似文献
65.
Govindasamy Rajarajan Natesan Jayachandramani Subramaniyan Manivarman Jayaraman Jayabharathi Venugopal Thanikachalam 《Transition Metal Chemistry》2008,33(3):393-397
The kinetics of oxidation of aldonitrones by 4-(dimethylamino)pyridinium chlorochromate (DMAPCC) has been studied in aqueous
N,N-dimethylformamide in the presence of perchloric acid. The reaction follows first-order kinetics with respect to each of DMAPCC
and nitrone. The order with respect to [H+] was found to be close to zero. The rate of oxidation was unaltered by the variation of [NaClO4] but addition of MnSO4 decreased the rate. The reaction rate was found to decrease with a decrease in dielectric constant of the medium. Electron-releasing
and electron-withdrawing groups perturb the reaction rate with a good Hammett correlation. The oxidation products were found
to be benzaldehyde and nitrosobenzene. The reaction was carried out at four different temperatures and the activation parameters
have been calculated. On the basis of the experimental findings, a suitable mechanism has been proposed. 相似文献
66.
The heme peroxidase-catalyzed iodination of human angiotensins I and II is described. It is observed that lactoperoxidase (LPO) can effectively and selectively iodinate the tyrosyl residues in angiotensin peptides. The thiourea/thiouracil-based peroxidase inhibitors effectively inhibit the iodination reactions, indicating that iodination is an enzymatic reaction and the mechanism of iodination is similar to that of peroxidase-catalyzed iodination of thyroglobulin. This study also shows that the monoiodo Ang I is a better substrate for the angiotensin converting enzyme than the native peptide. 相似文献
67.
Dr. Amit A. Vernekar Tandrila Das Prof. Dr. Govindasamy Mugesh 《Angewandte Chemie (International ed. in English)》2016,55(4):1412-1416
Organophosphorus‐based nerve agents, such as paraoxon, parathion, and malathion, inhibit acetylcholinesterase, which results in paralysis, respiratory failure, and death. Bacteria are known to use the enzyme phosphotriesterase (PTE) to break down these compounds. In this work, we designed vacancy‐engineered nanoceria (VE CeO2 NPs) as PTE mimetic hotspots for the rapid degradation of nerve agents. We observed that the hydrolytic effect of the nanomaterial is due to the synergistic activity between both Ce3+ and Ce4+ ions located in the active site‐like hotspots. Furthermore, the catalysis by nanoceria overcomes the product inhibition generally observed for PTE and small molecule‐based PTE mimetics. 相似文献
68.
69.
John U Kuriakose S Nair KP 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,68(2):331-336
The near infrared vibrational overtone absorption spectrum of liquid phase o-fluorophenol is examined in the region deltav=2, 3 and 4. The OH frequencies are compared with that of o-chlorophenol and phenol. Considering the relative electronegativities of all halogens, one might expect the order of intramolecular hydrogen bond strength for o-fluorophenol to be the greatest among all halogenophenols. It is evident that o-fluorophenol forms a weaker intramolecular hydrogen bond (an anomalous trend) contrary to that expected from relative electronegativities of halogens. The local mode mechanical frequency values and anharmonicity values obtained from fitting the overtones are analysed. Our observation is in agreement with the previous experimental as well as the recent theoretical vibrational analysis of halogenophenols using density functional theory (B3LYP). The overtone spectra of o-fluorophenol in carbon tetrachloride in different concentrations are also examined. It is noted that the OH-red shift which arises due to the intermolecular bond formation between the cis and trans conformers of o-fluorophenol (dimerization) increases with concentration. 相似文献
70.
Gupta LK Bansal U Chandra S 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,66(4-5):972-975
Nickel(II) complexes of isatin-3,2'-quinolyl-hydrazones of the type [Ni(L)X] (where X=Cl-, Br-, NO3-, CH3COO- and ClO4-] and their adducts Ni(L)X.2Y [where Y=pyridine or dioxane and X=Cl-, Br-, NO3- and ClO4-] have been synthesized under controlled experimental conditions and characterized by using the modern spectroscopic and physicochemical techniques viz. mass, 1H NMR, IR, electronic, elemental analysis, magnetic moment susceptibility measurements and molar conductance, etc. On the basis of spectral studies a four coordinated tetrahedral geometry is assigned for Ni(L)X type complexes whereas the adducts (Ni(L)X.2Y) were found to have a six coordinated distorted octahedral geometry. 相似文献