Optical and electrochemical properties of hydrogen-bonded phenol-pyrrolidino[60]fullerenes

Gary F. Moore, Jackson D. Megiatto, Michael Hambourger, Miguel Gervaldo, Gerdenis Kodis, Thomas A Moore, John Devens Gust, Ana L Moore

Research output: Contribution to journalArticle

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Abstract

We report the photophysical and electrochemical properties of phenol-pyrrolidino[60]fullerenes 1 and 2, in which the phenol hydroxyl group is ortho and para to the pyrrolidino group, respectively, as well as those of a phenyl-pyrrolidino[60]fullerene model compound, 3. For the ortho analog 1, the presence of an intramolecular hydrogen bond is supported by 1H NMR and FTIR characterization. The redox potential of the phenoxyl radical-phenol couple in this architecture is 240 mV lower than that observed in the associated para compound 2. Further, the C60 excited-state lifetime of the hydrogen-bonded compound 1 in benzonitrile is 260 ps, while the corresponding lifetime for 2 is identical to that of the model compound 3 at 1.34 ns. Addition of excess organic acid to a benzonitrile solution of 1 gives rise to a new species, 4, with an excited-state lifetime of 1.40 ns. In nonpolar aprotic solvents such as toluene, all three compounds have a C60 excited-state lifetime of ∼1 ns. These results suggest that the presence of an intramolecular H-bond in 1 poises the potential of phenoxyl radical-phenol redox couple at a value that it is thermodynamically capable of reducing the photoexcited fullerene. This is not the case for the para analog 2 nor is it the case for the protonated species 4. This work illustrates that in addition to being used as light activated electron acceptors, pyrrolidino fullerenes are also capable of acting as built-in proton-accepting units that influence the potential of an attached donor when organized in an appropriate molecular design.

Original languageEnglish
Pages (from-to)1018-1025
Number of pages8
JournalPhotochemical and Photobiological Sciences
Volume11
Issue number6
DOIs
Publication statusPublished - Jun 1 2012

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Phenol
Electrochemical properties
phenols
fullerenes
Hydrogen
Optical properties
Excited states
Fullerenes
optical properties
life (durability)
hydrogen
Oxidation-Reduction
analogs
excitation
Organic acids
Toluene
Fourier Transform Infrared Spectroscopy
Hydroxyl Radical
toluene
Protons

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Medicine(all)

Cite this

Optical and electrochemical properties of hydrogen-bonded phenol-pyrrolidino[60]fullerenes. / Moore, Gary F.; Megiatto, Jackson D.; Hambourger, Michael; Gervaldo, Miguel; Kodis, Gerdenis; Moore, Thomas A; Gust, John Devens; Moore, Ana L.

In: Photochemical and Photobiological Sciences, Vol. 11, No. 6, 01.06.2012, p. 1018-1025.

Research output: Contribution to journalArticle

Moore, Gary F. ; Megiatto, Jackson D. ; Hambourger, Michael ; Gervaldo, Miguel ; Kodis, Gerdenis ; Moore, Thomas A ; Gust, John Devens ; Moore, Ana L. / Optical and electrochemical properties of hydrogen-bonded phenol-pyrrolidino[60]fullerenes. In: Photochemical and Photobiological Sciences. 2012 ; Vol. 11, No. 6. pp. 1018-1025.
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