نتایج جستجو برای: detailed reaction mechanism

تعداد نتایج: 1105602  

Journal: :Bulletin of the Chemical Society of Japan 1969

Journal: :Bulletin of the Chemical Society of Japan 1971

Journal: :Bioorganic & medicinal chemistry 2002
Shengmin Sang Xiaofang Cheng Ruth E Stark Robert T Rosen Chung S Yang Chi-Tang Ho

Tea catechins, an important class of polyphenols, have been shown to have wide spectrum of antitumor activity believed to be due mainly to their antioxidative effect. In this study, the radical scavenging behavior of catechins on 2,2-diphenyl-1-picrylhydrazyl (DPPH) was studied. Two reaction products of (+)-catechin, and two reaction products of (-)-epicatechin were purified and identified. The...

Journal: :Journal of the American Chemical Society 2003
Liana D Socaciu Jan Hagen Thorsten M Bernhardt Ludger Wöste Ulrich Heiz Hannu Häkkinen Uzi Landman

Temperature-dependent rf-ion trap mass spectrometry and first-principles simulations reveal the detailed reaction mechanism of the catalytic gas-phase oxidation of CO by free Au(2)(-) ions in the presence of O(2). A metastable intermediate with a mass of Au(2)CO(3)(-) was observed at low temperatures. Two alternative structures corresponding to digold carbonate or peroxyformate are predicted fo...

Journal: :Physical review letters 2002
I Passchier L D van Buuren D Szczerba R Alarcon Th S Bauer D J Boersma J F J van Den Brand H J Bulten R Ent M Ferro-Luzzi M Harvey P Heimberg D W Higinbotham S Klous H Kolster J Lang B L Militsyn D Nikolenko G J L Nooren B E Norum H R Poolman I Rachek M C Simani E Six H de Vries K Wang Z-L Zhou

The spin-momentum correlation parameter A(V)(ed) was measured for the 2H-->(e-->,e'p)n reaction for missing momenta up to 350 MeV/c at Q2 = 0.21 (GeV/c)(2) for quasielastic scattering of polarized electrons from vector-polarized deuterium. The data give detailed information about the deuteron spin structure and are in good agreement with the results of microscopic calculations based on realisti...

Journal: :Physical chemistry chemical physics : PCCP 2009
Oliver Warschkow Irene Gao Steven R Schofield Daniel R Belcher Marian W Radny Sherin A Saraireh Phillip V Smith

Using density functional theory, we report detailed reaction path calculations for the reaction of acetone with the silicon (001) surface. We identify the key reaction intermediates of dissociative adsorption and the transition states between them. This resolves the identity of the one-dimer intermediate observed in STM experiments and its role in the formation of several two-dimer-wide end pro...

Journal: :Journal of the American Chemical Society 2002
K C Nicolaou P S Baran Y-L Zhong S Barluenga K W Hunt R Kranich J A Vega

The discovery and development of the o-iodoxybenzoic acid (IBX) reaction with certain unsaturated N-aryl amides (anilides) to form heterocycles are described. The application of the method to the synthesis of delta-lactams, cyclic urethanes, hydroxy amines, and amino sugars among other important building blocks and intermediates is detailed. In addition to the generality and scope of this cycli...

2008

The detailed mechanism of the reaction was further clarified by Martin et al4) in 1963 by investigating the relationship between the molecular structure of hemoglobin and the rate of the oxidation by nitrite. In these studies, however, the significance of the initial phase of the reaction, which will be clarified in the present paper, was insufficiently understood. As shown in Fig. 1, two phase...

The present paper deals with the kinetics and mechanism of homogeneously Ir(III) chloride catalyzed oxidation of D-mannitol by chloramine-T [CAT] in perchloric acid medium in the temperature range of 30 to 45 0C. The reaction is carried out in the presence of mercuric acetate as a scavenger for chloride ion. The experimental results show first order kinetics with respect to the oxidant [CAT] an...

Journal: :Chemical communications 2015
Terumasa Kato Shin-ichi Matsuoka Masato Suzuki

N-Heterocyclic carbenes (NHCs) promote the transfer hydrogenation of various activated C=C, C=N, and N=N bonds with water as the proton source. The NHCs act as reducing reagents to be converted into their oxides. A detailed reaction mechanism is proposed on the basis of deuterium-labeling experiments.

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