Porphyrin pyrrole sequencing: Low-energy collision-induced dissociation of (M + 7H) sup + generated in situ during ammonia chemical ionization
Journal Article
·
· Analytical Chemistry (Washington); (United States)
- Oak Ridge National Laboratory, TN (USA)
- Univ. of Tennessee, Knoxville (USA)
A method for pyrrole sequencing of porphyrins, based on high-pressure ammonia chemical ionization mass spectrometry/mass spectrometry (CI-MS/MS), is presented. High-pressure ammonia CI of porphyrins promotes formation of reduced molecular species and tri-, di-, and monopyrrolic fragment ions. The masses and pattern of the pyrrolic fragment ions can be used to determine the pyrrole sequence of the porphyrin. However, because of the complex ion source chemistry involved, these CI mass spectra are difficult to reproduce and are complicated by a plethora of structurally uninformative peaks. As such, pyrrole sequence elucidation based on the CI mass spectrum alone can be arduous, especially in the case of asymmetrically substituted porphyrins. In this paper, the MS/MS daughter ion spectrum of in situ formed (M + 7H){sup +} (i.e., the protonated porphyrinogen) is used to determine the porphyrin pyrrole sequence. Low-energy (30-100 eV) collision-induced dissociation (CID) of (M + 7H){sup +}, using a hybrid mass spectrometer of BEqQ geometry, yields, specific patterns of tri-, di-, and monopyrrolic daughter ions from which the pyrrole sequence of the porphyrin and combined mass of the substituents on the individual pyrroles can be determined. Several porphyrins of different pyrrole sequence are used to demonstrate the CI-MS/MS sequencing method. The capability of the CI-MS/MS method to sequence the pyrroles of porphyrins within a simple mixture of nonisobaric porphyrins is also demonstrated.
- OSTI ID:
- 5468263
- Journal Information:
- Analytical Chemistry (Washington); (United States), Journal Name: Analytical Chemistry (Washington); (United States) Vol. 62:8; ISSN ANCHA; ISSN 0003-2700
- Country of Publication:
- United States
- Language:
- English
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Structure elucidation of geoporphyrins by desorption tandem mass spectrometry: Carbon-number, pyrrolic structure, and sequence information from one experiment
Journal Article
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· Energy and Fuels; (USA)
·
OSTI ID:6125957
Mechanism of porphyrin reduction and decomposition in a high-pressure chemical ionization plasma
Journal Article
·
Wed Aug 02 00:00:00 EDT 1989
· Journal of the American Chemical Society; (USA)
·
OSTI ID:7155559
Structure elucidation of geoporphyrins by desorption tandem mass spectrometry: Carbon-number, pyrrolic structure, and sequence information from one experiment
Conference
·
Tue Feb 28 23:00:00 EST 1989
· American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA)
·
OSTI ID:7183256
Related Subjects
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400102* -- Chemical & Spectral Procedures
AMMONIA
AZOLES
CARBOXYLIC ACIDS
DATA
EXPERIMENTAL DATA
HETEROCYCLIC ACIDS
HETEROCYCLIC COMPOUNDS
HYDRIDES
HYDROGEN COMPOUNDS
INFORMATION
IONIZATION
MASS SPECTROSCOPY
NITROGEN COMPOUNDS
NITROGEN HYDRIDES
NUMERICAL DATA
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PORPHYRINS
PYRROLES
SPECTROSCOPY
400102* -- Chemical & Spectral Procedures
AMMONIA
AZOLES
CARBOXYLIC ACIDS
DATA
EXPERIMENTAL DATA
HETEROCYCLIC ACIDS
HETEROCYCLIC COMPOUNDS
HYDRIDES
HYDROGEN COMPOUNDS
INFORMATION
IONIZATION
MASS SPECTROSCOPY
NITROGEN COMPOUNDS
NITROGEN HYDRIDES
NUMERICAL DATA
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PORPHYRINS
PYRROLES
SPECTROSCOPY