Mossbauer spectroscopic studies of the six-coordinate heme-nitric oxide complex of iron(III) octaethylporphyrin N-methylimidazole, the first model ofthe nitrophorin-NO complexes

Citation
V. Schunemann et al., Mossbauer spectroscopic studies of the six-coordinate heme-nitric oxide complex of iron(III) octaethylporphyrin N-methylimidazole, the first model ofthe nitrophorin-NO complexes, ISR J CHEM, 40(1), 2000, pp. 9-14
Citations number
49
Categorie Soggetti
Chemistry
Journal title
ISRAEL JOURNAL OF CHEMISTRY
ISSN journal
00212148 → ACNP
Volume
40
Issue
1
Year of publication
2000
Pages
9 - 14
Database
ISI
SICI code
0021-2148(2000)40:1<9:MSSOTS>2.0.ZU;2-N
Abstract
The NO, N-methylimidazole complex of isotopically enriched octaethylporphyr inatoiron(III) chloride, [(OEPFe)-Fe-57(NO)(N-MeIm)Cl-+(-) has been prepare d in dimethylacetamide solution and studied by low-temperature Mossbauer sp ectroscopy in the presence and absence of a magnetic field. This complex is a model for the Fe(III)-NO complexes of the nitrophorins of the blood-suck ing insect, Rhodnius prolixus, where NO is released from the histidine-coor dinated ferrihemin center of each of the proteins upon the insect's injecti on of the saliva into the victim. The [OEPFe(NO)(N-MeIm)]Cl-+(-) complex is EPR silent and behaves as a diamagnetic species, with quadrupole splitting Delta E-Q = 1.64 mm s(-1), asymmetry parameter eta = 0.4, isomer shift del ta = 0.02 mm s(-1), and linewidth Gamma = 0.3 mm s(-1). Two electron config urations, Fe(III)-NO (low-spin d(5), strongly antiferromagnetically coupled to NO), or Fe(II)-NO+ (low-spin d(6), purely diamagnetic), are possible. W hich is the actual configuration cannot be determined until detailed molecu lar calculations are carried out. The low-spin OEPFe(III)-bis-N-methylimida zole complex also present in this sample has EPR g-values, quadrupole split ting, isomer shift, and hyperfine splittings typical of rhombic low-spin fe rriheme centers.