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