Synthesis and characterization of a new NLO-active donor-acceptor-type conjugated polymer derived from 3,4-diphenylthiophene

A new donor-acceptor-type conjugated polymer (P1) carrying 3,4-diphenylthiophene, 2,5-dihexyloxybenzene, and 1,3,4-oxadiazole units was synthesized through multistep reactions. The polymer was prepared using a polyhydrazide precursor route. The polymer has a well-defined structure and exhibits good...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of polymer research 2010-07, Vol.17 (4), p.495-502
Hauptverfasser: Manjunatha, M. G, Adhikari, Airody Vasudeva, Hegde, Pramod Kumar, Suchand Sandeep, C. S, Philip, Reji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:A new donor-acceptor-type conjugated polymer (P1) carrying 3,4-diphenylthiophene, 2,5-dihexyloxybenzene, and 1,3,4-oxadiazole units was synthesized through multistep reactions. The polymer was prepared using a polyhydrazide precursor route. The polymer has a well-defined structure and exhibits good thermal stability, with a decomposition onset temperature in nitrogen of 300 °C. Cyclic voltammetry experiments revealed that the polymer has low-lying LUMO (−3.68 eV) and high-lying HOMO (−5.78 eV) energy levels. The electrochemical band gap was found to be 2.10 eV. The UV-visible absorption spectrum of the polymer presented a maximum at 373 nm, and it displayed bluish-green fluorescence in dilute chloroform solution. The nonlinear optical properties of the new polymer were investigated at 532 nm using the Z-scan technique with nanosecond laser pulses. The polymer exhibited strong optical limiting behavior due to excited state absorption, which was phenomenologically similar to a three-photon absorption (3PA) process. The 3PA coefficient γ was found to be 7 × 10⁻²² m³/W². The studies show that the new polymer (P1) is a promising material for developing efficient photonic devices.
ISSN:1022-9760
1572-8935
DOI:10.1007/s10965-009-9336-1