TY - JOUR
T1 - Crystal structure and optical properties of n-pyrrole end-capped thiophene/phenyl co-oligomer
T2 - Strong h-type excitonic coupling and emission self-waveguiding
AU - Tavazzi, Silvia
AU - Miozzo, Luciano
AU - Silvestri, Leonardo
AU - Mora, Stefano
AU - Spearman, Peter
AU - Moret, Massimo
AU - Rizzato, Silvia
AU - Braga, Daniele
AU - Diagne Diaw, Abdou Karim
AU - Gningue-Sall, Diariatou
AU - Aaron, Jean Jacques
AU - Yassar, Abderrahim
PY - 2010/5/5
Y1 - 2010/5/5
N2 - In view of their exploitation in working devices, mainly for their emission properties, the interest in crystals of thiophene/phenylene co-oligomers has recently increased. Here, we describe the strategies for the organic synthesis and crystal growth of a novel oligothiophene-based co-oligomer (thiophene/phenyl co-oligomer end-capped with pyrrole) designed to explore the effect of an electron-rich aromatic ring, such as pyrrole, to end-cap oligothiophenes. The growth by the melted material is also discussed and suggested for implementation in real devices. The UV-visible optical characterization is provided, and the results (absorption and emission excitonic transitions, H-type aggregation, self-waveguiding of the emitted light) are interpreted on the basis of the crystallographic data in the regime of strong intermolecular coupling.
AB - In view of their exploitation in working devices, mainly for their emission properties, the interest in crystals of thiophene/phenylene co-oligomers has recently increased. Here, we describe the strategies for the organic synthesis and crystal growth of a novel oligothiophene-based co-oligomer (thiophene/phenyl co-oligomer end-capped with pyrrole) designed to explore the effect of an electron-rich aromatic ring, such as pyrrole, to end-cap oligothiophenes. The growth by the melted material is also discussed and suggested for implementation in real devices. The UV-visible optical characterization is provided, and the results (absorption and emission excitonic transitions, H-type aggregation, self-waveguiding of the emitted light) are interpreted on the basis of the crystallographic data in the regime of strong intermolecular coupling.
U2 - 10.1021/cg100113h
DO - 10.1021/cg100113h
M3 - Article
AN - SCOPUS:77952031984
SN - 1528-7483
VL - 10
SP - 2342
EP - 2349
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 5
ER -