TY - JOUR
T1 - Collision energetics in a tandem time-of-flight (TOF/TOF) mass spectrometer with a curved-field reflectron
AU - Ilchenko, Serguei
AU - Cotter, Robert J.
N1 - Funding Information:
This work was supported by a grant to RJC (GM64402) from the National Institutes of Health and a contract (N01 HV28180) to J. Van Eyk from the National Heart Lung and Blood Institute.
PY - 2007/9/1
Y1 - 2007/9/1
N2 - Collisions of fullerene ions (C60+) with helium and neon were carried out over a range of laboratory energies (3-20 keV) on a unique tandem time-of-flight (TOF/TOF) mass spectrometer equipped with a curved-field reflectron (CFR). The CFR enables focusing of product ions over a wide kinetic energy range. Thus, ions extracted from a laser desorption/ionization (LDI) source are not decelerated prior to collision, and collision energies in the laboratory frame are determined by the source extraction voltages. Comparison of product ion mass spectra obtained following collisions with inert gases show a time (and apparent mass) shift for product ions relative to those observed in spectra obtained by metastable dissociation (unimolecular decay), consistent with impulse collision models, in which interactions of helium with fullerene in the high energy range are primarily with a single carbon atom. In addition, within a narrow range of kinetic energies an additional peak corresponding to the capture of helium is observed for fragment ions C50+, C52+, C54+, C56+ and C58+.
AB - Collisions of fullerene ions (C60+) with helium and neon were carried out over a range of laboratory energies (3-20 keV) on a unique tandem time-of-flight (TOF/TOF) mass spectrometer equipped with a curved-field reflectron (CFR). The CFR enables focusing of product ions over a wide kinetic energy range. Thus, ions extracted from a laser desorption/ionization (LDI) source are not decelerated prior to collision, and collision energies in the laboratory frame are determined by the source extraction voltages. Comparison of product ion mass spectra obtained following collisions with inert gases show a time (and apparent mass) shift for product ions relative to those observed in spectra obtained by metastable dissociation (unimolecular decay), consistent with impulse collision models, in which interactions of helium with fullerene in the high energy range are primarily with a single carbon atom. In addition, within a narrow range of kinetic energies an additional peak corresponding to the capture of helium is observed for fragment ions C50+, C52+, C54+, C56+ and C58+.
KW - Collision energetics
KW - Curved-field reflectron
KW - Fullerenes
KW - Impulse collision theory
KW - Time-of-flight mass spectrometry
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U2 - 10.1016/j.ijms.2007.06.006
DO - 10.1016/j.ijms.2007.06.006
M3 - Article
C2 - 21731425
AN - SCOPUS:34447534547
SN - 1387-3806
VL - 265
SP - 372
EP - 381
JO - International Journal of Mass Spectrometry and Ion Processes
JF - International Journal of Mass Spectrometry and Ion Processes
IS - 2-3
ER -