Electrochemistry and spectra of six coordinated high-spin bis(tetrahydrofurane) protoporphyrinato IX - iron encapsulated in aqueous surfactant micelles

Authors
Citation
Dk. Das et Ok. Medhi, Electrochemistry and spectra of six coordinated high-spin bis(tetrahydrofurane) protoporphyrinato IX - iron encapsulated in aqueous surfactant micelles, I J CHEM A, 37(11), 1998, pp. 980-984
Citations number
21
Categorie Soggetti
Chemistry
Journal title
INDIAN JOURNAL OF CHEMISTRY SECTION A-INORGANIC BIO-INORGANIC PHYSICAL THEORETICAL & ANALYTICAL CHEMISTRY
ISSN journal
03764710 → ACNP
Volume
37
Issue
11
Year of publication
1998
Pages
980 - 984
Database
ISI
SICI code
0376-4710(199811)37:11<980:EASOSC>2.0.ZU;2-M
Abstract
The optical spectra of the bis (tetrahydrofurane) adduct of iron(III) and i ron(II) protoporphyrinato IX in aqueous solutions of anionic (SDS), cationi c (CTAB), and neutral (Triton X-100) surfactant micelles are typical of six -coordinated high-spin (6 cHS) ferrous and ferric hemes. The characteristic spectral bands in the ferric form are observed at. 400, 575 nm and 598 nm while these in the ferrous form are found at 420, 540 nm and 567 nm. The 6 cHS ferrous heme is very rare and the complex reported here is the first ex ample in aqueous solutions. The mid-point potential of the bis(thf) adducts of heme are -0.35 V, -0.36 V and -3.0V vs. Ag-AgCl in SDS, TX-100 and CTAB micelles, respectively. Binding of thf to iron porphyrin in SDS micelles g ives a 67 mV anodic shift of the potential. As the high-spin iron is brough t into the porphyrin plane in the six-coordinated bis (thf) complexes, the ferrous porphyrin is preferentially stabilised compared to the ferric hemin . The displcement of the iron atom to the porphyrin plane influence the cha rge transfer bands and the mid-point potential to a significant extent.