Abstract:A new diketopyrrolopyrrole derivative 1 exhibits excellent hole mobilities of 0.7 cm(2) V(-1) s(-1) and a current on/off ratio of 10(6) under ambient conditions in bottom-gate, top-contact organic thin film transistors (OTFTs) fabricated by vacuum deposition.
“…Additionally, owing to their reversible redox behaviour, these chromophores recorded different hyperpolarizability values in each of the two redox states and a high on/off (β on /β off ) ratio. Among the various known acceptors such as thiazole, 32 and benzodiazthiazole, 33 diketopyrrolopyrrole unit [34][35][36] has emerged a promising candidate for optoelectronics 37 and organic photovoltaics 34,38 such as organic light emitting diodes (OLEDs), [39][40][41] organic field effect transistors (OFETs), [42][43][44] organic solar cells (OSCs), [45][46][47] dye sensitized solar cells (DSSCs) [48][49] etc. This sub-unit has two amide groups that make it a strong acceptor, and consequently the energy of the lowest unoccupied molecular orbital (LUMO) of D-A or D-π-A systems, wherein appropriately substituted diketopyrrolopyrrole is used as acceptor, is considerably lowered.…”
A set of new ferrocene-diketopyrrolopyrrole (Fc-DPP) conjugated dyads was synthesized and their optical, nonlinear optical (NLO) and electrochemical properties were investigated. The second-order nonlinear polarizabilities were determined using Hyper-Rayleigh Scattering with femtosecond pulsed laser light at 840 nm. The dyads depicted structure dependent NLO response, which could be explained by correlating optical as well as electrochemical data. In the latter case, it is shown that the amplitude of the Fc based one-electron redox process of D-π-A type dyads is doubled in the dyads of the type D-π-A-π-D, where the acceptor (DPP) is flanked by two Fc donors.
Please do not adjust marginsPlease do not adjust margins diisopropyl succinate (8.10 g, 40 mmol) over a period of 1 h. Reaction mixture was heated at 85 °C for 2 h, after which it was cooled to 50 °C and 50 ml methanol was added. The reaction mixture was neutralized using glacial acetic acid and stirred for 15 min. and then cooled to ambient temperature and the contents were filtered over sintered glass (G4) funnel. Residue was washed twice with hot methanol and de-ionized water to yield analytically pure dark red solid 1 (61%). Mp> 300 o C IR (KBr): ν max 1628, 1648, 3153 and 3417 cm -1 .
“…Additionally, owing to their reversible redox behaviour, these chromophores recorded different hyperpolarizability values in each of the two redox states and a high on/off (β on /β off ) ratio. Among the various known acceptors such as thiazole, 32 and benzodiazthiazole, 33 diketopyrrolopyrrole unit [34][35][36] has emerged a promising candidate for optoelectronics 37 and organic photovoltaics 34,38 such as organic light emitting diodes (OLEDs), [39][40][41] organic field effect transistors (OFETs), [42][43][44] organic solar cells (OSCs), [45][46][47] dye sensitized solar cells (DSSCs) [48][49] etc. This sub-unit has two amide groups that make it a strong acceptor, and consequently the energy of the lowest unoccupied molecular orbital (LUMO) of D-A or D-π-A systems, wherein appropriately substituted diketopyrrolopyrrole is used as acceptor, is considerably lowered.…”
A set of new ferrocene-diketopyrrolopyrrole (Fc-DPP) conjugated dyads was synthesized and their optical, nonlinear optical (NLO) and electrochemical properties were investigated. The second-order nonlinear polarizabilities were determined using Hyper-Rayleigh Scattering with femtosecond pulsed laser light at 840 nm. The dyads depicted structure dependent NLO response, which could be explained by correlating optical as well as electrochemical data. In the latter case, it is shown that the amplitude of the Fc based one-electron redox process of D-π-A type dyads is doubled in the dyads of the type D-π-A-π-D, where the acceptor (DPP) is flanked by two Fc donors.
Please do not adjust marginsPlease do not adjust margins diisopropyl succinate (8.10 g, 40 mmol) over a period of 1 h. Reaction mixture was heated at 85 °C for 2 h, after which it was cooled to 50 °C and 50 ml methanol was added. The reaction mixture was neutralized using glacial acetic acid and stirred for 15 min. and then cooled to ambient temperature and the contents were filtered over sintered glass (G4) funnel. Residue was washed twice with hot methanol and de-ionized water to yield analytically pure dark red solid 1 (61%). Mp> 300 o C IR (KBr): ν max 1628, 1648, 3153 and 3417 cm -1 .
“…Recently, our group reported a p-channel, symmetrically functionalized (with thiophenyl group) molecular DPP derivative for OFETs with a highest hole mobility of 0.4 cm 2 /Vs [17]. Suraru et al has also reported a p-channel small molecular DPP derivative functionalized with cyanyl group for OFETs with field-effect mobility of 0.7 cm 2 /Vs [18]. OFETs based on n-channel DPP-T-DCV (functionalized with dicyanovinyl group) has been reported by Yoon et al with an electron mobility of 0.96 cm 2 /Vs (single crystalline) and 0.64 cm 2 /Vs (film) [19].…”
“…The 1,4-diketo-3,6-diphenylpyrrolo [3,4-c]pyrrole (DPP) derivatives have excellent chemical, thermal and photochemical stabilities and have attracted wide attention in the field of functional materials such as field-effect transistor [35][36][37][38] and polymer solar cells [39][40][41]. On the one hand, unmodified DPP emits green fluorescence but it can reach the near-infrared region after modification.…”
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