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Gas phase ion chemistry is a field of science encompassed within both chemistry and physics. It is the science that studies ions and molecules in the gas phase, most often enabled by some form of mass spectrometry. By far the most important applications for this science is in studying the thermodynamics and kinetics of reactions.
Usually, this mechanism is used in gas phase decomposition and also in isomerization reactions. An example of isomerization by a Lindemann mechanism is the isomerization of cyclopropane. [11] cyclo−C 3 H 6 → CH 3 −CH=CH 2. Although it seems like a simple reaction, it is actually a multistep reaction: cyclo−C 3 H 6 → CH 2 −CH 2 −CH ...
Heterogeneous catalysis typically involves solid phase catalysts and gas phase reactants. [2] In this case, there is a cycle of molecular adsorption, reaction, and desorption occurring at the catalyst surface. Thermodynamics, mass transfer, and heat transfer influence the rate (kinetics) of reaction.
In such cases, the momentum of the reaction trajectory from the reactants to the intermediate can carry forward to affect product selectivity. An example of such a reaction is the ring closure of cyclopentane biradicals generated from the gas-phase thermal decomposition of 2,3-diazabicyclo[2.2.1]hept-2-ene. [20] [21]
This is a gas-phase reaction of phosphorus vapor, above the solid, with oxygen producing excited states of (PO) 2 and HPO. [7] Another gas phase reaction is the basis of nitric oxide detection in commercial analytic instruments applied to environmental air-quality testing.
The rate for a bimolecular gas-phase reaction, A + B → product, predicted by collision theory is [6] = = ()where: k is the rate constant in units of (number of molecules) −1 ⋅s −1 ⋅m 3.
The higher the proton affinity, the stronger the base and the weaker the conjugate acid in the gas phase.The (reportedly) strongest known base is the ortho-diethynylbenzene dianion (E pa = 1843 kJ/mol), [3] followed by the methanide anion (E pa = 1743 kJ/mol) and the hydride ion (E pa = 1675 kJ/mol), [4] making methane the weakest proton acid [5] in the gas phase, followed by dihydrogen.
Grote–Hynes theory is a theory of reaction rate in a solution phase. This rate theory was developed by James T. Hynes with his graduate student Richard F. Grote in 1980. [1] The theory is based on the generalized Langevin equation (GLE). This theory introduced the concept of frequency dependent friction for