Skip to main content
. Author manuscript; available in PMC: 2010 Feb 1.
Published in final edited form as: J Inorg Biochem. 2008 Oct 10;103(2):174–181. doi: 10.1016/j.jinorgbio.2008.09.017

Table 1.

Properties of iron-porphyrin complexes.

Complex UV-visible (nm)a 1H NMR (δ)b μeffB)c
(TPP)FeIII(ClO4) (1a) 398 (5.11), 532 74.6, 18.3, 11.9, 11.7
(TMP)FeIII(ClO4) (1b) 399 (5.07), 530 8.4, 3.6, 2.6, −26
(OEP)FeIII(ClO4) (1c) 376 (4.92), 503, 553, 634, 559 47.0, 8.3
(TPP)FeIV(ClO4)2 (2a) 396 (5.14), 532 69.6, 31.6, 16.9 2.96
(TMP)FeIV(ClO4)2 (2b) 397 (5.12), 530 66, 32, 14 3.03
(OEP)FeIV(ClO4)2 (2c) 391 (5.02), 495, 618
(TPP)+•FeIII(ClO4)2 (3a) 393 (5.03), 535, 602, 682 61.8, 32.8, −11.1, −14.2 5.50
(TMP)+•FeIII(ClO4)2 (3b) 392 (4.98), 498, 605, 680 92, 71.7, 31.4, 20.8 5.95
(OEP)+•FeIII(ClO4)2 (3c) 374 (4.85), 502, 595, 648 69.8, 26.9 5.20
a

UV-visible spectral absorbances in CH3CN; log ε of the Soret band in parentheses.

b

NMR spectra in CD3CN solution at −40 °C.

c

Effective magnetic moment determined in CD3CN at −40 °C.