Slow electron transfer rates for fluorinated cobalt porphyrins: Electronic and conformational factors modulating metalloporphyrin ET

Haoran Sun, Valeriy V. Smirnov, Stephen G. DiMagno

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

The electron transfer (ET) properties of a series of closely related cobalt porphyrins, [2,3,7,8,12,13,17,18-octafluoro-5,10,15,20-tetrakis(pentafluorophenyl) porphyrinato]cobalt, CoF28TPP, [2,3,7,8,12,13,17,18-octafluoro-5,10,15,20-tetraphenyl)porphyrinato]cobalt, CoF8TPP, 5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato]cobalt, CoF20TPP, and [5,10,15,20-tetraphenylporphyrinato]cobalt, CoTPP, were investigated by cyclic voltammetry, cyclic voltammetric digital simulation, in situ UV-vis and IR spectroelectrochemistry, kinetic ET studies, bulk electrolysis, 19F NMR spectroscopy, X-ray crystallography, and molecular modeling. In benzonitrile containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as supporting electrolyte, the ET rate constants for the Co2+/3+ redox couples were found to be strongly substituent dependent; the heterogeneous ET rate constant (kel) varied by a factor of 104, and the ET self-exchange rate constants (kex) varied over 7 orders of magnitude for the compounds studied. The remaining observed ring oxidation and metal and ring reduction events exhibited nearly identical kel values for all compounds. UV-vis and IR spectroelectrochemistry, bulk electrolysis, and 19F NMR spectroscopic studies support attribution of different ET rates to widely varying inner sphere reorganization energies (λi) for these closely related compounds. Structural and semiempirical (PM3) studies indicate that the divergent kinetic behavior of CoTPP, CoF8TPP, CoF 20TPP, and CoF28TPP first oxidations arises mainly from large nuclear reorganization energies primarily associated with core contraction and dilation. Taken together, these studies provide rational design principles for modulating ET rate constants in cobalt porphyrins over an even larger range and provide strategies for similar manipulation of ET rates in other porphyrin-based systems: substituents that lower C-C, C-N, and N-M vibrational frequencies or minimize porphyrin orbital overlap with the metal-centered orbital undergoing a change in electron population will increase kET. The heme ruffling apparent in electron transfer proteins such as cytochrome c is interpreted as nature's exploitation of this design strategy.

Original languageEnglish (US)
Pages (from-to)6032-6040
Number of pages9
JournalInorganic Chemistry
Volume42
Issue number19
DOIs
StatePublished - Sep 22 2003

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

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