A detailed study on the thermal, photo-physical and electrochemical properties and OFET applications of D–π–A–π–D structured unsymmetrical diketopyrrolopyrrole materials. Issue 115 (4th November 2015)

• Record Type: Journal Article
• Authors: Bharath, D.; Chithiravel, S.; Sasikumar, M.; Chereddy, Narendra Reddy; Shanigaram, Balaiah; Bhanuprakash, K.; Krishnamoorthy, K.; Rao, V. Jayathirtha
• Is Part Of: RSC advances. Volume 5:Issue 115(2015)
• Page Start: 94859
• Page End: 94865
• Publication Date: 2015-11-04
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra16653e
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Seven unsymmetrical DPP-derivatives with a D–π–A–π–D architecture have been synthesized and the effect of the electron donating ability and extent of electronic conjugation of the end capping units on their properties are explored. Abstract : A series of seven unsymmetrical diketopyrrolopyrrole (DPP) derivatives with donor–pi–acceptor–pi–donor (D–π–A–π–D) architecture have been designed, synthesized and well characterised. The effect of the electron donating capacity and extent of electronic conjugation of the end-capping units on the thermal, photo-physical and electrochemical properties of the synthesized materials was thoroughly investigated using various experimental techniques and theoretical calculations. Organic field-effect transistors (OFETs) were fabricated using these materials to obtain their hole/electron transporting characteristics. All these materials showed moderate to good hole transporting ability, and the OFET fabricated using the DPP-derivative with benzofuran and pyrene end groups exhibited a hole mobility of 6.7 × 10 −4 cm 2 V −1 s −1 with V T of −9 V. The observed photo-physical, electrochemical, thermal, and charge carrier properties of the synthesized DPP-derivatives indicated their applicability in various areas like organic photovoltaics, disposable electronics and biomedical devices.