Infrared multiple photon dissociation (IRMPD) is a technique used in mass spectrometry to fragment molecules in the gas phase usually for structural analysis of the original (parent) molecule.[1]
How it works
An infrared laser is directed through a window into the vacuum of the mass spectrometer where the ions are. The mechanism of fragmentation involves the absorption by a given ion of multiple infrared photons. The parent ion becomes excited into more energetic vibrational states until a bond(s) is broken resulting in gas phase fragments of the parent ion. In the case of powerful laser pulses, the dissociation proceeds via inner-valence ionization of electrons.[2][3]
IRMPD is most often used in Fourier transform ion cyclotron resonance mass spectrometry.[4]
Infrared photodissociation spectroscopy
By applying intense tunable IR lasers, like IR-OPOs or IR free electron lasers, the wavelength dependence of the IRMPD yield can be studied.[5] This infrared photodissociation spectroscopy allows for the measurement of vibrational spectra of (unstable) species that can only be prepared in the gas phase. Such species include molecular ions but also neutral species like metal clusters that can be gently ionized after interaction with the IR light for their mass spectrometric detection.[6]
Isotope separation
Due to the relatively large differences in IR absorption frequencies that are due to different resonance frequencies for molecules containing different isotopes, this technique has been suggested as a way to perform Isotope separation with difficult-to-separate isotopes, in a single pass. For example, molecules of UF6 containing U-235 might be ionized completely as a result of such a laser resonance, leaving UF6 containing the heavier U-238 intact.
See also
Infrared spectroscopy
Tandem mass spectrometry
Photodissociation
Blackbody infrared radiative dissociation
Electron capture dissociation
Collision-induced dissociation is another, more common, method to fragment gas phase ions.
References
Little DP, Speir JP, Senko MW, O'Connor PB, McLafferty FW (1994). "Infrared multiphoton dissociation of large multiply charged ions for biomolecule sequencing". Anal. Chem. 66 (18): 2809–15. doi:10.1021/ac00090a004. PMID 7526742.
Talebpour; et al. (1999). "Multiphoton ionization of inner-valence electrons and fragmentation of ethylene in an intense Ti:sapphire laser pulse". Chemical Physics Letters. 313 (5–6): 789–794. Bibcode:1999CPL...313..789T. doi:10.1016/s0009-2614(99)01075-1.
Talebpour; et al. (2000). "Dissociative ionization of benzene in intense ultra-fast laser pulses". J. Phys. B: At. Mol. Opt. Phys. 33 (21): 4615–4626. Bibcode:2000JPhB...33.4615T. doi:10.1088/0953-4075/33/21/307.
Laskin J, Futrell JH (2005). "Activation of large ions in FT-ICR mass spectrometry". Mass Spectrometry Reviews. 24 (2): 135–67. Bibcode:2005MSRv...24..135L. doi:10.1002/mas.20012. PMID 15389858.
Polfer, Nick C.; Oomens, J (2007). "Reaction products in mass spectrometry elucidated with infrared spectroscopy". Physical Chemistry Chemical Physics. 9 (29): 3804–17. Bibcode:2007PCCP....9.3804P. doi:10.1039/b702993b. PMID 17637973.
Gruene P, Rayner DM, Redlich B, van der Meer AF, Lyon JT, Meijer G, Fielicke A (2008). "Structures of Neutral Au7, Au19, and Au20 Clusters in the Gas Phase". Science. 321 (5889): 674–6. Bibcode:2008Sci...321..674G. doi:10.1126/science.1161166. hdl:11858/00-001M-0000-0010-FC2A-A. PMID 18669858.
vte
Mass spectrometry
Mass m/z Mass spectrum MS software Acronyms
Ion source
AMS APCI APLI CI DAPPI DART DESI DIOS EESI EI ESI FAB FD GD IA ICP LAESI MALDI MALDESI MIP PTR SESI SIMS SS SSI SELDI TI TS
Mass analyzer
Sector Wien filter Time-of-flight Quadrupole mass filter Quadrupole ion trap Penning trap FT-ICR Orbitrap
Detector
Electron multiplier Microchannel plate detector Daly detector Faraday cup Langmuir–Taylor detector
MS combination
MS/MS QqQ Hybrid MS GC/MS LC/MS IMS/MS CE-MS
Fragmentation
BIRD CID ECD EDD ETD HCD IRMPD NETD SID
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