Observation of different reactivities of para and ortho-water towards trapped diazenylium ions
Water is one of the most fundamental molecules in chemistry, biology and astrophysics. It exists as two distinct nuclear-spin isomers, para- and ortho-water, which do not interconvert in isolated molecules. The experimental challenges in preparing pure samples of the two isomers have thus far precluded a characterization of their individual chemical behavior. Capitalizing on recent advances in the electrostatic deflection of polar molecules, we separate the ground states of para- and ortho-water in a molecular beam to show that the two isomers exhibit different reactivities in a prototypical reaction with trapped diazenylium ions. Based on ab initio calculations and a modelling of the reaction kinetics using rotationally adiabatic capture theory, we rationalize this finding in terms of different rotational averaging of ion-dipole interactions during the reaction.
This water isomer phenomenon is probably very significant in biology and may also explain the quantum nature of certain biochemical interactions.
Also it's from Nature so very reliable.
This is mostly outside my knowledge and understanding, but the first thing that comes to mind is the effect of isotopes.
Isomers are different than isotopes but I get what you are getting at... and yes both may have variable affinities in chemical reactions.
I should have answered that differently. Isomers have identical molecular mass. These isomers only differ in that the hydrogen atom spin is either identical (ortho) or opposite (para) which is a very slight difference on the atomic scale yet the para form is more reactive.
I guess my question is more about correlation between isotopes and ortho/para varieties. Especially when talking about pure samples of either ortho or para.
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