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81.
Neha Patel Minhajul Arfeen Tejender Singh Shweta Bhagat Ajay Sakhare Prasad V. Bharatam 《Journal of computational chemistry》2020,41(31):2624-2633
Nitreones are compounds with oxidation state 1 at the nitrogen, these compounds carry formal positive charge as well as two lone pairs of electrons at nitrogen center. These compounds are also known as divalent NI compounds and can be represented with the general formula L → N+ ← L, where L is an electron donating ligand. In the recent past, several divalent NI compounds have been reported with L = N-heterocyclic carbene (NHC), remote N-heterocyclic carbene (rNHC), carbocyclic carbene (CCC) and diaminocarbene. Recently, our group reported that a novel six-membered CCC (cyclohexa-2,5-diene-4-[diaminomethynyl]-1-ylidene) can stabilize N+ center in nitreones. As an independent carbene, this species is very unstable. In this work, modulation of this CCC using (a) annulation, (b) heterocyclic ring modification, (c) substitutions adjacent to the carbenic carbon, (d) exocyclic double bond insertion and (e) ring contraction, has been reported. These modulations and quantum chemical analyses helped in the identification of five new six-membered CCCs which carry improved donation and stability properties. Further, these CCCs were employed in the design of new divalent NI compounds (nitreones) which carry coordination bonds between ligands and N+ center. The molecular and electronic structure properties, and the donor→acceptor coordination interactions present in the resultant low oxidation state divalent NI compounds have been explored. 相似文献
82.
We analyse the evolution of a two-stage chemical reaction betweentwo neighbouring plumes of reactants. Under the assumption thatthe plumes are approximately Gaussian we derive a system ofordinary differential equations for the total amount, the centroidand the variance of each reactant. We compare the solution ofthese equations with full numerical simulation of the reaction.Excellent agreement is obtained, with solution of the near-Gaussianmodel requiring considerably less computational effort thanthe full simulations. Of key importance is the yield of thereaction, and we discuss this feature in particular. 相似文献
83.
B. K. Sharma S. L. S. Sarowha S. D. Bhagat R. K. Tiwari S. K. Gupta P. S. Venkataramani 《Fresenius' Journal of Analytical Chemistry》1998,360(5):539-544
Hydrocarbon group type analysis is important in all conversion processes and in preparation of feed for these conversion
processes so as to learn the selectivity of the different type of catalysts for product yield and quality. The use of the
Mark 5 Iatroscan detector and the method reported here allowed for a rapid and quantitative hydrocarbon group type analysis
of petroleum residues without prior separation of asphaltenes. SARA type analyses of petroleum residues have been performed
by a three stage development using n-hexane, toluene and DCM (95%):MeOH (5%). The standard deviation and coefficient of variation
in repeated measurements by this method were as low as 0.65 wt% or less and 3.5 wt% or less, respectively. The time required
for analysis of 10 samples could be as short as 90 min.
Received: 20 May 1997 / Revised: 12 August 1997 / Accepted: 16 August 1997 相似文献
84.
P. Karthikeyan Rajenahally V. Jagadeesh Y. Sree Sandhya Puttaswamy P. Nithya S. Senthil Kumar P.R. Bhagat 《应用有机金属化学》2011,25(1):34-46
Ruthenium, osmium and ruthenium + osmium catalyzed synthetic methodology was developed for the synthesis of anthranilic acids from indoles in good to excellent yields using bromamine‐B in alkaline acetonitrile–water (1:1) at 313 K. Detailed catalysis studies of ruthenium, osmium and the mixture of both were carried out for the synthetic reactions. The positive synergistic catalytic activity of Ru(III) + Os(VIII) was observed to a large extent with the activity greater than the sum of their separate catalytic activities. Detailed kinetic and mechanistic investigations for each catalyzed reactions were carried out. The kinetic pattern and mechanistic picture of each catalyzed reaction were found to be different for each catalyst and to obey the underlying rate laws: where, x, y < 1. The reactions were studied at different temperatures and the activation parameters were evaluated for each catalyzed reaction. Under the identical set of experimental conditions, the kinetics of all the three catalyzed reactions were compared with uncatalyzed reactions, revealing that the catalyzed reactions were 6‐ to 42‐fold faster. The catalytic efficiency of aforementioned catalysts followed the order: Ru(III) + Os(VIII) > Os(VIII) > Ru(III). This trend may be attributed to the different d‐electronic configuration of the catalysts. The proposed mechanisms and the rigorous kinetic models derived give results that fit well with the experimental data in each catalyzed reaction. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
85.
A straightforward, efficient and more sustainable catalyst-free method has been developed for the synthesis of quinoxaline, benzoxazole, and benzimidazole ring system in glycerol to achieve yields that were comparable to or better than, those in conventional media. It is noteworthy that the reaction was exclusively carried out in glycerol-water system, rendering the methodology highly valuable from both environment and economic points of view. 相似文献
86.
Virinder Bhagat Dr. Julia Schumann Prof. Dr. Holger F. Bettinger 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(55):12654-12663
The reaction of dioxygen with nitrenes can have significant energy barriers, although both reactants are triplet diradicals and the formation of nitroso-O-oxides is spin-allowed. By means of matrix-isolation infrared spectroscopy in solid argon, nitrogen, and neon, and through high-level computational quantum chemistry, it is shown herein that a 3-nitreno-1,3,2-benzodioxaborole CatBN (Cat=catecholato) reacts with dioxygen under cryogenic conditions thermally at temperatures as low as 7 K to produce two distinct products, an anti-nitroso-O-oxide and a nitritoborane CatBONO. The computed barriers for the formation of nitroso-O-oxide isomers are very low. Whereas anti-nitroso-O-oxide is kinetically trapped, its bisected isomer has a very low barrier for metathesis, yielding the CatBO+NO radicals in a strongly exothermic reaction; these radicals can combine under matrix-isolation conditions to give nitritoborane CatBONO. The trapped isomer, anti-nitroso-O-oxide, can form the nitritoborane CatBONO only after photoexcitation, possibly involving isomerization to the bisected isomer of anti-nitroso-O-oxide. 相似文献
87.
Balinge Kamlesh Rudreshwar Datir Sagar Krushnarao Khajone Vijay Baburao Bhansali Karan Jivanlal Khiratkar Avinash Ganesh Bhagat Pundlik Rambhau 《Research on Chemical Intermediates》2019,45(2):155-168
Research on Chemical Intermediates - Benzimidazoles are important bioactive compounds with diverse applications in the medicinal, industrial, as well as agrochemical fields. In this study, an... 相似文献
88.
Parasuraman Karthikeyan Prashant Narayan Muskawar Sachin Arunrao Aswar Pundlik Rambhau Bhagat Suresh Kumar Sythana 《应用有机金属化学》2012,26(11):562-569
A novel, effective 1‐glycyl‐3‐methyl imidazolium chloride–palladium(II) complex ([Gmim]Cl–Pd(II)) was synthesized and studied as an organocatalyst for the Sonogashira coupling reaction under solvent‐free conditions at 25 °C. The hydrophobic group on amino acid favors reagent diffusion toward the chloroglycine moiety, increasing the catalytic activity of supported palladium complex. By this protocol, different aryl halides (Cl, Br and I) were reacted with phenylacetylene in good to excellent yields with turnover number 8.0 × 102 to 9.6 × 102. The catalyst was recycled for the reaction of bromobenzene with phenylacetylene for eight runs without appreciable loss of its catalytic activity and negligible metal leaching. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
89.
90.