Binding energies in large ionic clusters from kinetic energy release measurements

The determination of binding energy is a very important piece of information that an experiment can provide. We have devised a new experimental procedure to measure binding energies for unimolecular (metastable) decay of multiply charged metal ligand cluster ions in gas phase. The new technique c...

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Main Author: Bruzzi, Eleonora
Format: Thesis (University of Nottingham only)
Language:English
Published: 2014
Subjects:
Online Access:https://eprints.nottingham.ac.uk/73690/
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author Bruzzi, Eleonora
author_facet Bruzzi, Eleonora
author_sort Bruzzi, Eleonora
building Nottingham Research Data Repository
collection Online Access
description The determination of binding energy is a very important piece of information that an experiment can provide. We have devised a new experimental procedure to measure binding energies for unimolecular (metastable) decay of multiply charged metal ligand cluster ions in gas phase. The new technique consists in preparing clusters by supersonic expansion, and in generating metal ligand clusters by pick up technique. A high resolution double focusing mass spectrometer having reversed sector geometry is used to obtain mass analysed ion kinetic energy spectra. The evaporative ensemble statistical model by C. E. Klots is used to analyse the kinetic energy releases and to obtain the corresponding binding energies. Our new experimental method has been applied to measure the binding energy for the loss of one neutral molecule in a unimolecular (metastable) dissociation in H+(H2O)n , *H +(NH3)n and H+(CH 3OH)n for n ≤ 30. The main results were: (i) for n > 6 each fragmentation corresponds to breaking one hydrogen bond (ii) no magic numbers were observed. This experimental procedure was used to measure the binding energy for theloss of one neutral molecule in the unimolecular (metastable) decay of [M(L)n2+ for n ≤ 20, where M = Mg, Ca, Sr and L = H2O, NH 3, CH 3 OH. This investigation determined that: (i) the coordination number is six for all the metal solvent cluster ions, except for [Mg(NH3 n]2+ having coordination number equal to four; (ii) the double charge affects the binding interactions on the solvation shells up to n = 20 with the exception of [Sr(H2O)n]2+, for which n = 14; (iii) binding energies correspond to breaking one hydrogen bond; (iv) no magic numbers were detected. * Printed version:”H+(H2O)n, H+(H2O)n,and H+(CH3OH)n for n ≤ 30.” correct version ”H+(H2O)n, H+(NH3)n,and H+(CH3OH)n for n ≤ 30.”
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format Thesis (University of Nottingham only)
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institution University of Nottingham Malaysia Campus
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language English
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publishDate 2014
recordtype eprints
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spelling nottingham-736902023-06-05T09:54:33Z https://eprints.nottingham.ac.uk/73690/ Binding energies in large ionic clusters from kinetic energy release measurements Bruzzi, Eleonora The determination of binding energy is a very important piece of information that an experiment can provide. We have devised a new experimental procedure to measure binding energies for unimolecular (metastable) decay of multiply charged metal ligand cluster ions in gas phase. The new technique consists in preparing clusters by supersonic expansion, and in generating metal ligand clusters by pick up technique. A high resolution double focusing mass spectrometer having reversed sector geometry is used to obtain mass analysed ion kinetic energy spectra. The evaporative ensemble statistical model by C. E. Klots is used to analyse the kinetic energy releases and to obtain the corresponding binding energies. Our new experimental method has been applied to measure the binding energy for the loss of one neutral molecule in a unimolecular (metastable) dissociation in H+(H2O)n , *H +(NH3)n and H+(CH 3OH)n for n ≤ 30. The main results were: (i) for n > 6 each fragmentation corresponds to breaking one hydrogen bond (ii) no magic numbers were observed. This experimental procedure was used to measure the binding energy for theloss of one neutral molecule in the unimolecular (metastable) decay of [M(L)n2+ for n ≤ 20, where M = Mg, Ca, Sr and L = H2O, NH 3, CH 3 OH. This investigation determined that: (i) the coordination number is six for all the metal solvent cluster ions, except for [Mg(NH3 n]2+ having coordination number equal to four; (ii) the double charge affects the binding interactions on the solvation shells up to n = 20 with the exception of [Sr(H2O)n]2+, for which n = 14; (iii) binding energies correspond to breaking one hydrogen bond; (iv) no magic numbers were detected. * Printed version:”H+(H2O)n, H+(H2O)n,and H+(CH3OH)n for n ≤ 30.” correct version ”H+(H2O)n, H+(NH3)n,and H+(CH3OH)n for n ≤ 30.” 2014-07-15 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en cc_by https://eprints.nottingham.ac.uk/73690/1/Bruzzi_Eleonora_PhD_Thesis_2014.pdf Bruzzi, Eleonora (2014) Binding energies in large ionic clusters from kinetic energy release measurements. PhD thesis, University of Nottingham. metal ligand binding binding energy clusters thermodynamics thermochemistry gas phase solvated ion kinetic energy pick up technique ion beams mass spectrometry
spellingShingle metal ligand binding
binding energy
clusters
thermodynamics
thermochemistry
gas phase solvated ion
kinetic energy
pick up technique
ion beams
mass spectrometry
Bruzzi, Eleonora
Binding energies in large ionic clusters from kinetic energy release measurements
title Binding energies in large ionic clusters from kinetic energy release measurements
title_full Binding energies in large ionic clusters from kinetic energy release measurements
title_fullStr Binding energies in large ionic clusters from kinetic energy release measurements
title_full_unstemmed Binding energies in large ionic clusters from kinetic energy release measurements
title_short Binding energies in large ionic clusters from kinetic energy release measurements
title_sort binding energies in large ionic clusters from kinetic energy release measurements
topic metal ligand binding
binding energy
clusters
thermodynamics
thermochemistry
gas phase solvated ion
kinetic energy
pick up technique
ion beams
mass spectrometry
url https://eprints.nottingham.ac.uk/73690/