Literature DB >> 18834102

Investigation of energy deposited by femtosecond electron transfer in collisions using hydrated ion nanocalorimetry.

Anne I S Holm1, William A Donald, Preben Hvelplund, Mikkel K Larsen, Steen Brøndsted Nielsen, Evan R Williams.   

Abstract

Ion nanocalorimetry is used to investigate the internal energy deposited into M (2+)(H 2O) n , M = Mg ( n = 3-11) and Ca ( n = 3-33), upon 100 keV collisions with a Cs or Ne atom target gas. Dissociation occurs by loss of water molecules from the precursor (charge retention) or by capture of an electron to form a reduced precursor (charge reduction) that can dissociate either by loss of a H atom accompanied by water molecule loss or by exclusively loss of water molecules. Formation of bare CaOH (+) and Ca (+) by these two respective dissociation pathways occurs for clusters with n up to 33 and 17, respectively. From the threshold dissociation energies for the loss of water molecules from the reduced clusters, obtained from binding energies calculated using a discrete implementation of the Thomson liquid drop model and from quantum chemistry, estimates of the internal energy deposition can be obtained. These values can be used to establish a lower limit to the maximum and average energy deposition. Not taking into account effects of a kinetic shift, over 16 eV can be deposited into Ca (2+)(H 2O) 33, the minimum energy necessary to form bare CaOH (+) from the reduced precursor. The electron capture efficiency is at least a factor of 40 greater for collisions of Ca (2+)(H 2O) 9 with Cs than with Ne, reflecting the lower ionization energy of Cs (3.9 eV) compared to Ne (21.6 eV). The branching ratio of the two electron capture dissociation pathways differs significantly for these two target gases, but the distributions of water molecules lost from the reduced precursors are similar. These results suggest that the ionization energy of the target gas has a large effect on the electron capture efficiency, but relatively little effect on the internal energy deposited into the ion. However, the different branching ratios suggest that different electronic excited states may be accessed in the reduced precursor upon collisions with these two different target gases.

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Year:  2008        PMID: 18834102      PMCID: PMC2646606          DOI: 10.1021/jp8019655

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  26 in total

1.  Secondary and tertiary structures of gaseous protein ions characterized by electron capture dissociation mass spectrometry and photofragment spectroscopy.

Authors:  HanBin Oh; Kathrin Breuker; Siu Kwan Sze; Ying Ge; Barry K Carpenter; Fred W McLafferty
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-20       Impact factor: 11.205

2.  Electron capture dissociation distinguishes a single D-amino acid in a protein and probes the tertiary structure.

Authors:  Christopher M Adams; Frank Kjeldsen; Roman A Zubarev; Bogdan A Budnik; Kim F Haselmann
Journal:  J Am Soc Mass Spectrom       Date:  2004-07       Impact factor: 3.109

3.  Effects of charge state and cationizing agent on the electron capture dissociation of a peptide.

Authors:  Anthony T Iavarone; Kolja Paech; Evan R Williams
Journal:  Anal Chem       Date:  2004-04-15       Impact factor: 6.986

4.  Differences between the internal energy depositions induced by collisional activation and by electron transfer of W(CO)6(2+) ions on collision with Ar and K targets.

Authors:  Shigeo Hayakawa; Akihiro Kitaguchi; Satoko Kameoka; Michisato Toyoda; Toshio Ichihara
Journal:  J Chem Phys       Date:  2006-06-14       Impact factor: 3.488

5.  Divalent metal ion-peptide interactions probed by electron capture dissociation of trications.

Authors:  Haichuan Liu; Kristina Håkansson
Journal:  J Am Soc Mass Spectrom       Date:  2006-09-06       Impact factor: 3.109

6.  On the survival of peptide cations after electron capture: role of internal hydrogen bonding and microsolvation.

Authors:  Tapas Chakraborty; Anne I S Holm; Preben Hvelplund; Steen Brøndsted Nielsen; Jean-Christophe Poully; Esben S Worm; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2006-08-22       Impact factor: 3.109

7.  On the mechanism of electron-capture-induced dissociation of peptide dications from 15n-labeling and crown-ether complexation.

Authors:  Anne I S Holm; Preben Hvelplund; Umesh Kadhane; Mikkel Koefoed Larsen; Bo Liu; Steen Brøndsted Nielsen; Subhasis Panja; Jan Mondrup Pedersen; Troels Skrydstrup; Kristian Støchkel; Evan R Williams; Esben S Worm
Journal:  J Phys Chem A       Date:  2007-09-12       Impact factor: 2.781

8.  Electron super-rich radicals in the gas phase. A neutralization-reionization mass spectrometric and ab initio/RRKM study of diaminohydroxymethyl and triaminomethyl radicals.

Authors:  Changtong Hao; Jennifer L Seymour; Frantisek Turecek
Journal:  J Phys Chem A       Date:  2007-08-17       Impact factor: 2.781

9.  Effects of electron kinetic energy and ion-electron inelastic collisions in electron capture dissociation measured using ion nanocalorimetry.

Authors:  Jeremy T O'Brien; James S Prell; Anne I S Holm; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2008-03-05       Impact factor: 3.109

10.  Mechanism and energetics of intramolecular hydrogen transfer in amide and peptide radicals and cation-radicals.

Authors:  Frantisek Turecek; Erik A Syrstad
Journal:  J Am Chem Soc       Date:  2003-03-19       Impact factor: 15.419

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  4 in total

1.  Measuring the extent and width of internal energy deposition in ion activation using nanocalorimetry.

Authors:  William A Donald; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2009-12-28       Impact factor: 3.109

2.  Measuring internal energy deposition in collisional activation using hydrated ion nanocalorimetry to obtain peptide dissociation energies and entropies.

Authors:  Maria Demireva; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2010-03-09       Impact factor: 3.109

3.  Directly relating gas-phase cluster measurements to solution-phase hydrolysis, the absolute standard hydrogen electrode potential, and the absolute proton solvation energy.

Authors:  William A Donald; Ryan D Leib; Jeremy T O'Brien; Evan R Williams
Journal:  Chemistry       Date:  2009-06-08       Impact factor: 5.236

4.  Directly relating reduction energies of gaseous Eu(H2O)n(3+), n = 55-140, to aqueous solution: the absolute SHE potential and real proton solvation energy.

Authors:  William A Donald; Ryan D Leib; Maria Demireva; Jeremy T O'Brien; James S Prell; Evan R Williams
Journal:  J Am Chem Soc       Date:  2009-09-23       Impact factor: 15.419

  4 in total

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