EJMS Table of Contents

European Journal of Mass Spectrometry (EJMS)

Special Issue: Dedicated to Peter Derrick in recognition of his contributions to mass spectrometry

Eur. J. Mass Spectrom. Volume 15 Issue 2 (2009)

Pages 0–0

doi: 10.1255/ejms.991

Peter J. Derrick

Margaret Sheil

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Pages 73–81

doi: 10.1255/ejms.948

Characterisation of anthracyclines from a cosmomycin D- producing species of Streptomyces by collisionally-activated dissociation and ion mobility mass spectrometry

Celine Kelso,^a Juan Diego Rojas,^b Renata L.A. Furlan,^b Gabriel Padilla,^b,c and Jennifer L. Beck,^a
^aSchool of Chemistry, University of Wollongong, New South Wales, Australia 2522. E-mail: jbeck@uow.edu.au
^bInstitute of Biomedical Sciences, University of São Paulo, São Paulo, SP Brazil
^cSchool of Veterinary and Biomedical Sciences, James Cook University, Queensland, Australia 4811

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Pages 83–90

doi: 10.1255/ejms.945

Chemistry of (and on) transition metal clusters: a Fourier transform ion cyclotron resonance study of the reaction of niobium cluster cations with nitric oxide

Daniel J. Harding,^a Thomas A.A. Oliver,^a Tiffany R. Walsh,^a,b Thomas Drewello,^a,c D. Phil Woodruff,^d Peter J. Derrick^a,e,† and Stuart R. Mackenzie^a,f,*
^aDepartment of Chemistry, University of Warwick, Coventry, CV4 7AL, UK
^bCentre for Scientific Computing, University of Warwick, Coventry, CV4 7AL, UK
^cDepartment of Chemistry and Pharmacy, Physical Chemistry I, Friedrich-Alexander- Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen, Germany
^dDepartment of Physics, University of Warwick, Coventry, CV4 7AL, UK
^eMassey University, Institute of Fundamental Science, Private Bag 11 222, Palmerston North, New Zealand
^fUniversity Chemical Laboratories, Lensfield Road, Cambridge, CB2 1EW, UK. E-mail: srm49@cam.ac.uk; stuart.mackenzie@chem.ox.ac.uk

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Pages 91–104

doi: 10.1255/ejms.952

Anions [N(CH₂)₃]^– and [ON(CH₂)₂]^– are stable in the gas phase, but can they be charge stripped to form the radicals N(CH₂)₃ and ON(CH₂)₂? A joint experimental and theoretical study

Mark Fitzgerald, Suresh Dua, Daniel Bilusich, Peter C.H. Eichinger, Salvatore Peppe and John H. Bowie^*
Department of Chemistry, The University of Adelaide, South Australia, 5005. E-mail: john.bowie@adelaide.edu.au

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Pages 105–112

doi: 10.1255/ejms.944

Endocyclic versus exocyclic mechanisms for methyl migration in protonated N,N′-dimethylpropane-1,3-diamine.^d

Tom Waters^a,b,* and Richard A.J. O�Hair^a–c,*
^aSchool of Chemistry, University of Melbourne, Victoria 3010, Australia. E-mail: rohair@unimelb.edu.au
^bBio21 Institute of Molecular Science and Biotechnology, The University of Melbourne, Victoria 3010, Australia
^cARC Centre of Excellence in Free Radical Chemistry and Biotechnology

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Pages 113–130

doi: 10.1255/ejms.947

Deciphering drift time measurements from travelling wave ion mobility spectrometry-mass spectrometry studies

David P. Smith,^a Tom W. Knapman,^a Iain Campuzano,^b Richard W. Malham,^a Joshua T. Berryman,^a Sheena E. Radford^a and Alison E. Ashcroft^a,*
^aAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK. E-mail: a.e.ashcroft@leeds.ac.uk
^bWaters MS Technologies Centre, Floats Road, Wythenshaw, Manchester, M23 9LZ, UK

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Pages 131–144

doi: 10.1255/ejms.940

Trends in the Periodic System: the mass spectrum of dimethylphenyl phosphane and a comparison of the gas phase reactivity of dimethylphenyl pnictogene radical cations C₆H₅E(CH₃)₂^•+, (E = N, P, As)^†

Dirk Kirchhoff,^a Hans-Friedrich Grützmacher^a,* and Hansjörg Grützmacher^b
^aFakultät für Chemie der Universität Bielefeld, Postfach 10 01 31, D-33501 Bielefeld, Germany. E-mail: hans-friedrich.gruetzmacher@uni-bielefeld.de
^bDepartment of Chemistry and Applied Biosciences, H 131, ETH-Höggerberg, CH-8093 Zürich, Switzerland

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Pages 145–155

doi: 10.1255/ejms.941

Electron-capture dissociation and collision-induced dissociation of lanthanide metal–ligand complexes and lanthanide metal–ligand complexes bound to phosphopeptides

Jackie A. Mosely,^* Benjamin S. Murray, David Parker
Department of Chemistry, Durham University, South Road, Durham, DH1 3LE, UK. E-mail: jackie.mosely@durham.ac.uk

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Pages 157–166

doi: 10.1255/ejms.943

Nitro–nitrite isomerization and transition state switching in the dissociation of ionized nitromethane: a threshold photoelectron–photoion coincidence spectroscopy study

Brandon Ferrier,^a Anne-Marie Boulanger,^a David M.P. Holland,^b David A. Shaw^b and Paul M. Mayer^a,*
^aDepartment of Chemistry, University of Ottawa, 10 Marie-Curie, Ottawa, Ontario, Canada K1N 6N5. E-mail: pmmayer@uottawa.ca
^bDaresbury Laboratory, Daresbury, Warrington, Cheshire WA4 4AD UK

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Pages 167–181

doi: 10.1255/ejms.953

Energetics and reaction mechanisms for the competitive losses of H₂, CH₄ and C₂H₄ from protonated methylbenzenes—implications to the methanol-to-hydrocarbons (MTH) process^a

Osamu Sekiguchi,^a Verena Meyer,^b Matthias C. Letzel,^b Dietmar Kuck^b,* and Einar Uggerud^a,c,*
^aMass Spectrometry Laboratory, Department of Chemistry, University of Oslo, POB, 1033 Blindern, N-0315 Oslo, Norway
^bDepartment of Chemistry, Bielefeld University, POB 100131, D-33501 Bielefeld, Germany
^cCentre for Theoretical and Computational Chemistry (CTCC), Department of Chemistry, University of Oslo, POB 1033 Blindern, N-0315 Oslo, Norway

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Pages 183–188

doi: 10.1255/ejms.949

Heat of formation for the benzoyl cation by photoionization mass spectrometry

John C. Traeger
Department of Chemistry, La Trobe University, Victoria 3086, Australia. E-mail: j.traeger@latrobe.edu.au

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Pages 189–198

doi: 10.1255/ejms.960

Laser desorption/ablation plumes from capillary-like restricted volumes

Richard Knochenmuss
Novartis Institutes for Biomedical Research, WSJ 503.1104, 4052 Basel, Switzerland. E-mail: rknochenmuss@gmx.net

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Pages 199–208

doi: 10.1255/ejms.968

Gas-phase ion chemistry of protonated melatonin

David Bongiorno,^a Leopoldo Ceraulo,^a,* Lorenzo Camarda,^a Maurizio Ciofalo,^b Mirella Ferrugia,^a Serena Indelicato,^a Andrea Mele^c and Vincenzo Turco Liveri^d
^aDipartimento di Chimica e Tecnologie Farmaceutiche, Università di Palermo, Via Archirafi 32, I-90123 Palermo, Italy. E-mail: lceraulo@unipa.it
^bDipartimento di Ingegneria e Tecnologie Agro-Forestali, Sezione di Chimica, Università di Palermo, Viale delle Scienze, Edificio 4, I-90128 Palermo, Italy
^cDipartimento di Chimica, Materiali ed Ingegneria Chimica “G. Natta”–Politecnico di Milano, Via Mancinelli 7, I-20131, Milano, Italy
^dDipartimento di Chimica Fisica “F. Accascina”, Università di Palermo, Viale delle Scienze-Parco d�Orleans II, I-90128, Palermo, Italy

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Pages 209–220

doi: 10.1255/ejms.950

Positive ion chemistry of SiH₄/NF₃ gaseous mixtures studied by ion trap mass spectrometry

Paola Antoniotti,^a Lorenza Operti,^a Roberto Rabezzana,^a Francesca Turco,^a Stefano Borocci^b and Felice Grandinetti^b,*
^aDipartimento di Chimica Generale e Chimica Organica and NIS Centre of Excellence, Università di Torino, C.so M. D'Azeglio 48, 10125 Torino, Italy
^bDipartimento di Scienze Ambientali, Università della Tuscia, L.go dell' Università , s.n.c., 01100 Viterbo, Italy. E-mail: fgrandi@unitus.it

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Pages 221–230

doi: 10.1255/ejms.969

Gas-phase reactivity of acylphenols in electrospray and matrix- assisted laser desorption ionization mass spectrometry

Isabelle Schmitz-Afonso,^a Vincent Guérineau,^a Alessandra Maia- Grondard,^a Khalijah Awang,^b Marc Litaudon,^a Françoise Guéritte^a and Olivier Laprévote^a,*
^aCNRS, UPR2301–ICSN Mass Spectrometry Laboratory, Avenue de la Terrasse, Bat 27, 91198 Gif-sur- Yvette cedex, France. E-mail: olivier.laprevote@icsn.cnrs-gif.fr
^bDepartment of Chemistry, University of Malaya, Pantai Valley, Kuala Lumpur, Malaysia

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Pages 231–238

doi: 10.1255/ejms.946

Preliminary silylation for structure determination of oligomeric silsesquioxanes by matrix-assisted laser desorption/ionisation mass spectrometry

V.G. Zaikin,^a,* R.S. Borisov,^a N.Yu. Polovkov,^a S.N. Filatov^b and V.V. Kireev^b
^aTopchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky prospect 29, 119991 Moscow, Russia. E-mail: zaikin@ips.ac.ru
^bPolymer Chemistry and Technology Department, D. Mendeleev University of Chemical Technology of Russia, Moscow, Russia

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Pages 239–248

doi: 10.1255/ejms.970

Redshift or adduct stabilization—a computational study of hydrogen bonding in adducts of protonated carboxylic acids

Solveig Gaarn Olesen and Steen Hammerum^*
Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen Ø, Denmark. E-mail: steen@kiku.dk

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Pages 249–260

doi: 10.1255/ejms.967

Development of an ion trap/multi-turn time-of-flight mass spectrometer with potential-lift

Kenichi Iwamoto,^a Hirofumi Nagao^b and Michisato Toyoda^c
^aDepartment of Chemistry, Graduate School of Science, Osaka Prefecture University, 1-1 Gakuencho Nakaku, Sakai, Osaka 599- 8531, Japan
^bDivision of Sustainable Energy and Environmental Engineering, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0781, Japan
^cDepartment of Physics, Graduate School of Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan

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Pages 261–273

doi: 10.1255/ejms.959

Small (poly)unsaturated oxygen containing ions and molecules: a brief assessment of their thermochemistry based on computational chemistry

John L. Holmes^a,*, Karl J. Jobst^b and Johan K. Terlouw^b,*
^aChemistry Department, Ottawa University, Ottawa, ON K1N 6N5. Canada
^bChemistry Department, McMaster University, Hamilton, ON L8S 4M1. Canada

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Pages 275–281

doi: 10.1255/ejms.951

Electron capture dissociation, electron detachment dissociation and infrared multiphoton dissociation of sucrose octasulfate

Jeremy J. Wolff,^a Tatiana N. Laremore,^b Franklin E. Leach, III,^a Robert J. Linhardt^b–d and I. Jonathan Amster^a,*
^aDepartment of Chemistry, University of Georgia, Athens, GA 30602, USA. E-mail: jamster@uga.edu
^bDepartment of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute, Troy, NY 12180, USA
^cChemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA
^dDepartment of Biology, Rensselaer Polytechnic Institute, Troy, NY 12180, USA

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Pages 283–291

doi: 10.1255/ejms.962

Unintended parametric ejection of ions from an ion cyclotron resonance trap by two-electrode axialization

Franklin Martinez, Alexander Herlert, Gerrit Marx, Lutz Schweikhard and Noelle Walsh
Institut für Physik, Ernst-Moritz-Arndt-Universität Greifswald, D-17487 Greifswald, Germany. E-mail: martinez@physik.uni-greifswald.de

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Pages 293–304

doi: 10.1255/ejms.966

Characterization of oligodeoxynucleotide fragmentation pathways in infrared multiphoton dissociation and electron detachment dissociation by Fourier transform ion cyclotron double resonance

Jiong Yang^a,b and Kristina Håkansson^a,*
^aDepartment of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, MI 48109-1055, USA. E-mail: kicki@umich.edu
^aCurrent address: Bruker Daltonics, Manning Park, Billerica, MA 01821, USA

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Pages 305–314

doi: 10.1255/ejms.971

Dependence of the ejection velocities of laser-ablated ions on the laser wavelength and fluence

Chau-Wen Chou,^a Randall W. Nelson^b and Peter Williams^c
^aProteomics Core Facility and Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA
^bBiodesign Institute, Arizona State University, Tempe, AZ 85287-1604, USA
^cDepartment of Chemistry & Biochemistry, Arizona State University, Tempe, AZ 85287-1604, USA

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Pages 315–324

doi: 10.1255/ejms.972

Oxygen-containing diatomic dications in the gas phase

Jirí Fišer,^a Klaus Franzreb,^b Jan Lörinčík^c,d and Peter Williams^b,*
^aFaculty of Science, Department of Physical and Macromolecular Chemistry, Charles University, Hlavova 2030, 128 40 Prague, Czech Republic
^bDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287, USA. E-mail: pw@asu.edu
^cDepartment of Physics of the Faculty of Science, J.E. Purkyne University, Ceske mladeze 8, 400 96 Usti nad Labem, Czech Republic
^dInstitute of Photonics and Electronics, Academy of Sciences of the Czech Republic, Chaberska 57, 182 51 Praha 8, Czech Republic

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Pages 325–335

doi: 10.1255/ejms.987

Cu(II)-catalyzed reactions in ternary [Cu(AA)(AA – H)]⁺ complexes (AA = Gly, Ala, Val, Leu, Ile, t-Leu, Phe)

Ping Wang,^a,c Gilles Ohanessian^b and Chrys Wesdemiotis^a,*
^aDepartment of Chemistry, The University of Akron, Akron, OH 44325-3601, USA. E-mail: wesdemiotis@uakron.edu
^bLaboratoire des Mécanismes Réactionnels, Département de Chimie, Ecole Polytechnique, CNRS, F- 91128 Palaiseau Cedex, France
^cCurrent address: The Dow Chemical Company, 2301 N. Brazosport Blvd, B-1219 Freeport, TX 77541-3257, USA

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Pages 337–341

doi: 10.1255/ejms.988

On the electron affinity of B₂

Vassiliki-Alexandra Glezakou^a and Peter R. Taylor^b,*
^aPacific Northwest National Laboratory, PO Box 999, Richland, WA 99352, USA. E-mail: Vanda.Glezakou@pnl.gov
^bDepartment of Chemistry and Centre for Scientific Computing, University of Warwick, Coventry CV4 7AL, United Kingdom. Email: p.r.taylor@warwick.ac.uk

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Pages 343–348

doi: 10.1255/ejms.989

Application of effective potential approach to ion dynamics investigation in field asymmetric ion mobility spectrometry conditions

Eugene N. Nikolaev^a,* and Alexander A. Vedenov^b
^aThe Institute for Energy Problems of Chemical Physics, Russian Academy of Sciences, Leninskij pr.38 k.2, Moscow 119334, Russia. E-mail: ennikolaev@rambler.ru
^bKurchatov Institute for Atomic Energy, Ulitsa Kurchatova 46, Moscow 123182, Russia

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Pages 349–359

doi: 10.1255/ejms.990

Determination of the binding energies in aromatic clusters: resonance-enhanced multi-photon ionization and mass analyzed threshold ionization investigation of the dichlorobenzene—argon complexes

Angela Gaber,^a Mikko Riese,^a,b Frank Witte^a and Jürgen Grotemeyer^a,*
^aUniversity of Kiel, Ludewig-Meyn-Str. 8, Kiel, Germany. E-mail: grote@phc.uni-kiel.de
^bThe Photon Science Institute, Alan Turing Building, Oxford Road, Manchester M13 9PL, United Kingdom. E-mail: mikko.riese@manchester.ac.uk

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Pages 361–365

doi: 10.1255/ejms.942

Letter: Collision energy and cone voltage optimisation for glycopeptide analysis

Judit Krenyacz, László Drahos and Károly Vékey
Chemical Research Center, Hungarian Academy of Sciences, H-1025 Budapest, Pusztaszeri út 59-67, Hungary

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