TY - JOUR
T1 - Intra- and intermolecular photoinduced energy and electron transfer between oligothienylenevinylenes and N-methylfulleropyrrolidine
AU - Apperloo, J.J.
AU - Martineau, C.
AU - Hal, van, P.A.
AU - Roncali, J.
AU - Janssen, R.A.J.
PY - 2002
Y1 - 2002
N2 - The photophys. properties of a homologous series of oligothienylenevinylenes (nTVs) and the inter- and intramol. photoinduced energy- and electron-transfer processes between an nTV as a donor and N-methylfulleropyrrolidine (MP-C60) as an acceptor are described as a function of oligomer length (n = 2, 3, 4, 6, 8, 12) in apolar and polar solvents. Whereas the shorter oligomers fluoresce and have singlet excited-state [nTV(S1)] lifetimes of 280 ps (2TV) and 1360 ps (3TV), the S1 lifetimes of the longer oligomers (n > 3) are extremely short because of a fast thermal decay, resulting in negligible quantum yields for fluorescence and intersystem crossing to the triplet state [nTV(T1)]. Using photoinduced absorption (PIA) spectroscopy, the authors demonstrate, that the nTV(T1) state can be populated indirectly via intermol. triplet energy transfer using photoexcited MP-C60 as a triplet sensitizer for n > 2. This enabled the spectral detn. of the nTV (Tn -> T1) transition as a function of chain length (n = 3-12) in toluene (e = 2.38). In a more polar solvent, o-dichlorobenzene (ODCB, e = 9.93), the MP-C60(T1) state acts both as an oxidizing agent toward the nTVs, resulting in the formation of a metastable radical ion pair (nTV+.bul. + MP-C60-.bul.) for n > 2, and as a triplet sensitizer, to produce the nTV(T1) state. In addn. to the intermol. transfer reactions, the authors investigated the corresponding intramol. photoinduced energy- and electron-transfer reactions in systems in which MP-C60 and nTV (n = 2-4) are covalently linked. The results indicate that, after photoexcitation of the nTV moiety, an ultrafast singlet energy transfer to MP-C60 occurs, followed by an intramol. electron transfer. The intramolecularly charge-sepd. state is the lowest-energy excited state in polar media, e.g., ODCB. In apolar media, e.g., toluene, the formation of the intramolecularly charge-sepd. state occurs only for n > 2 and concurrent with fluorescence and intersystem crossing to the MP-C60(T1) state. The discrimination between energy and electron transfer is rationalized using a continuum model. [on SciFinder (R)]
AB - The photophys. properties of a homologous series of oligothienylenevinylenes (nTVs) and the inter- and intramol. photoinduced energy- and electron-transfer processes between an nTV as a donor and N-methylfulleropyrrolidine (MP-C60) as an acceptor are described as a function of oligomer length (n = 2, 3, 4, 6, 8, 12) in apolar and polar solvents. Whereas the shorter oligomers fluoresce and have singlet excited-state [nTV(S1)] lifetimes of 280 ps (2TV) and 1360 ps (3TV), the S1 lifetimes of the longer oligomers (n > 3) are extremely short because of a fast thermal decay, resulting in negligible quantum yields for fluorescence and intersystem crossing to the triplet state [nTV(T1)]. Using photoinduced absorption (PIA) spectroscopy, the authors demonstrate, that the nTV(T1) state can be populated indirectly via intermol. triplet energy transfer using photoexcited MP-C60 as a triplet sensitizer for n > 2. This enabled the spectral detn. of the nTV (Tn -> T1) transition as a function of chain length (n = 3-12) in toluene (e = 2.38). In a more polar solvent, o-dichlorobenzene (ODCB, e = 9.93), the MP-C60(T1) state acts both as an oxidizing agent toward the nTVs, resulting in the formation of a metastable radical ion pair (nTV+.bul. + MP-C60-.bul.) for n > 2, and as a triplet sensitizer, to produce the nTV(T1) state. In addn. to the intermol. transfer reactions, the authors investigated the corresponding intramol. photoinduced energy- and electron-transfer reactions in systems in which MP-C60 and nTV (n = 2-4) are covalently linked. The results indicate that, after photoexcitation of the nTV moiety, an ultrafast singlet energy transfer to MP-C60 occurs, followed by an intramol. electron transfer. The intramolecularly charge-sepd. state is the lowest-energy excited state in polar media, e.g., ODCB. In apolar media, e.g., toluene, the formation of the intramolecularly charge-sepd. state occurs only for n > 2 and concurrent with fluorescence and intersystem crossing to the MP-C60(T1) state. The discrimination between energy and electron transfer is rationalized using a continuum model. [on SciFinder (R)]
U2 - 10.1021/jp012936f
DO - 10.1021/jp012936f
M3 - Article
SN - 1089-5639
VL - 106
SP - 21
EP - 31
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 1
ER -