نتایج جستجو برای: H2 Elimination

تعداد نتایج: 80193  

Journal: :physical chemistry and electrochemistry 0

propene dissociation channels were characterized by ab initio ccsd(t)/6-311++g(d,p) calculations. inthis work the detailed mechanism of propene dissociation to c2h4+ch2, c2h2+h+ch3, c2h2+ch4 andc3h3+h2+h have been investigated. according to our calculations, ten fragments can be classified intofive dissociated channels. our results point out that two mechanisms come into play in the h2 eliminat...

Propene dissociation channels were characterized by ab initio CCSD(T)/6-311++g(d,p) calculations. Inthis work the detailed mechanism of propene dissociation to C2H4+CH2, C2H2+H+CH3, C2H2+CH4 andC3H3+H2+H have been investigated. According to our calculations, ten fragments can be classified intofive dissociated channels. Our results point out that two mechanisms come into play in the H2 eliminat...

Journal: :Journal of the American Society for Mass Spectrometry 2008

Journal: :Bulletin of mathematical biology 2003
Andreas Fahlman Susan R Kayar

We modelled the kinetics of H2 flux during gas uptake and elimination in conscious pigs exposed to hyperbaric H2. The model used a physiological description of gas flux fitted to the observed decompression sickness (DCS) incidence in two groups of pigs: untreated controls, and animals that had received intestinal injections of H2-metabolizing microbes that biochemically eliminated some of the H...

Journal: :Dalton transactions 2015
Ian Dance

The elimination of H2 from an M(H)2 component of a coordination complex is often described as reductive elimination, in which the H atoms are regarded as hydride ions, and the product complex after elimination is regarded as reduced by two electrons. The concept is M(n+2)(H(-))2 → M(n) + H2 (with oxidative addition as its reverse). This interpretation contravenes Pauling's electroneutrality pri...

Journal: :The journal of physical chemistry. A 2008
Ryan Z Hinrichs Jonathan J Schroden H Floyd Davis

The reactions of Y (a2D), Zr (a3F), Nb (a6D), Mo (a7S), and electronically excited-state Mo* (a5S) with propyne (methylacetylene) and 2-butyne (1,2-dimethylacetylene) were investigated using crossed molecular beams. For all of the metals studied, reactions with propyne led to H2 elimination, forming MC3H2. For Y + propyne, C-C bond cleavage forming YCCH + CH3 also was observed, with an energeti...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Zhi-Yong Yang Nimesh Khadka Dmitriy Lukoyanov Brian M Hoffman Dennis R Dean Lance C Seefeldt

Nitrogenase is activated for N2 reduction by the accumulation of four electrons/protons on its active site FeMo-cofactor, yielding a state, designated as E4, which contains two iron-bridging hydrides [Fe-H-Fe]. A central puzzle of nitrogenase function is an apparently obligatory formation of one H2 per N2 reduced, which would "waste" two reducing equivalents and four ATP. We recently presented ...

Journal: :The journal of physical chemistry. A 2007
Sandra Feyel Ludwig Scharfenberg Charles Daniel Hans Hartl Detlef Schröder Helmut Schwarz

Bare vanadium oxide and hydroxide cluster cations, V(m)O(n)+ and V(m)O(n-1) (OH)+ (m = 1-4, n = 1-10), generated by electrospray ionization, were investigated with respect to their reactivity toward methanol using mass spectrometric techniques. Several reaction channels were observed, such as abstraction of a hydrogen atom, a methyl radical, or a hydroxymethyl radical, elimination of methane, a...

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