Photophysics and redox properties of rylene imide and diimide dyes alkylated ortho to the imide groups

Joseph E. Bullock, Michael T. Vagnini, Charusheela Ramanan, Dick T Co, Thea M. Wilson, Jay W. Dicke, Tobin J Marks, Michael R Wasielewski

Research output: Contribution to journalArticle

74 Citations (Scopus)

Abstract

Ruthenium-catalyzed C-H bond activation was used to directly attach phenethyl groups derived from styrene to positions ortho to the imide groups in a variety of rylene imides and diimides including naphthalene-1,8- dicarboximide (NMI), naphthalene-1,4:5,8-bis(dicarboximide) (NI), perylene-3,4-dicarboximide (PMI), perylene-3,4:9,10-bis(dicarboximide) (PDI), and terrylene-3,4:11,12- bis(dicarboximide) (TDI). The monoimides were dialkylated, while the diimides were tetraalkylated, with the exception of NI, which could only be dialkylated due to steric hindrance. The absorption, fluorescence, transient absorption spectra, and lowest excited singlet state lifetimes of these chromophores, with the exception of NI, are nearly identical to those of their unsubstituted parent chromophores. The reduction potentials of the dialkylated chromophores are ∼100 mV more negative and oxidation potentials are ∼40 mV less positive than those of the parent compounds, while the corresponding potentials of the tetraalkylated compounds are ∼200 mV more negative and ∼100 mV less positive than those of their parent compounds, respectively. Continuous wave electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) data on the radical anion of PDI reveals spin density on the perylene-core protons as well as on the β-protons of the phenethyl groups. The phenethyl groups enhance the otherwise poor solubility of the bis(dicarboximide) chromophores and only weakly perturb the photophysical and redox properties of the parent molecules, rendering these derivatives and related molecules of significant interest to solar energy conversion.

Original languageEnglish
Pages (from-to)1794-1802
Number of pages9
JournalJournal of Physical Chemistry B
Volume114
Issue number5
DOIs
Publication statusPublished - Feb 11 2010

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Imides
Perylene
imides
Chromophores
chromophores
Coloring Agents
Dyes
dyes
Naphthalene
naphthalene
Protons
solar energy conversion
Molecules
Styrene
Ruthenium
protons
Energy conversion
Excited states
styrenes
Solar energy

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Materials Chemistry
  • Surfaces, Coatings and Films

Cite this

Photophysics and redox properties of rylene imide and diimide dyes alkylated ortho to the imide groups. / Bullock, Joseph E.; Vagnini, Michael T.; Ramanan, Charusheela; Co, Dick T; Wilson, Thea M.; Dicke, Jay W.; Marks, Tobin J; Wasielewski, Michael R.

In: Journal of Physical Chemistry B, Vol. 114, No. 5, 11.02.2010, p. 1794-1802.

Research output: Contribution to journalArticle

Bullock, Joseph E. ; Vagnini, Michael T. ; Ramanan, Charusheela ; Co, Dick T ; Wilson, Thea M. ; Dicke, Jay W. ; Marks, Tobin J ; Wasielewski, Michael R. / Photophysics and redox properties of rylene imide and diimide dyes alkylated ortho to the imide groups. In: Journal of Physical Chemistry B. 2010 ; Vol. 114, No. 5. pp. 1794-1802.
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