skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Photoinduced charge separation and stabilization in clusters of a fullerene-aniline dyad

Journal Article · · Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical
DOI:https://doi.org/10.1021/jp9915679· OSTI ID:20001119

Fullerene-bridge-aniline dyad and the model fulleropyrrolidine compound form stable, optically transparent clusters in mixtures (3:1) of acetonitrile and toluene. Ground- and excited-state properties of the clusters of the dyad and the model compound are compared with their corresponding monomeric forms. Clustering of the dyad as well as the model compound exhibits a red-shifted emission maximum ({lambda}{sub max} {approximately}738 nm) compared to their monomeric forms ({lambda}{sub max} {approximately}714 nm). The electron transfer from the appended electron donor moiety to the parent fullerene core in the dyad cluster is evident from the decreased ({approximately}80%) fluorescence yield. The formation of fullerene radical anion (absorption maximum at 1010nm) with a lifetime of several hundreds of microseconds was further confirmed using nanosecond laser (337 nm) flash photolysis experiments. In contrast, the dyad molecules in their monomeric form did not yield any detectable yield of C{sub 60} radical anion following laser pulse excitation. The failure to observe any charge-transfer intermediates following laser pulse excitation. The failure to observe any charge-transfer intermediates following laser pulse excitation, even in polar solvents such as benzonitrile or nitromethane, suggested that fast back-electron-transfer process must be operative in the monomeric dyad system. On the other hand, clustering of the fullerene-based dyads in a mixed-solvent system can provide a unique way to decrease the rate of back electron transfer, thus stabilizing the electron-transfer products.

Research Organization:
Regional Research Lab., Trivandrum (IN)
Sponsoring Organization:
USDOE
OSTI ID:
20001119
Journal Information:
Journal of Physical Chemistry B: Materials, Surfaces, Interfaces, amp Biophysical, Vol. 103, Issue 42; Other Information: PBD: 21 Oct 1999; ISSN 1089-5647
Country of Publication:
United States
Language:
English

Similar Records

Intramolecular electron transfer in fullerene/ferrocene based donor-bridge-acceptor dyads
Journal Article · Wed Feb 05 00:00:00 EST 1997 · Journal of the American Chemical Society · OSTI ID:20001119

Intramolecular energy transfer in fullerene pyrazine dyads
Journal Article · Thu Nov 26 00:00:00 EST 1998 · Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, amp General Theory · OSTI ID:20001119

Reduction potential of the sulfhydryl radical: Pulse radiolysis and laser flash photolysis studies of the formation and reactions of {sm_bullet}SH and HSSH{sm_bullet}{sup {minus}} in aqueous solutions
Journal Article · Thu Jul 08 00:00:00 EDT 1999 · Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, amp General Theory · OSTI ID:20001119