Diketopyrrolopyrrole-based functional supramolecular polymers: next-generation materials for optoelectronic applications

Ghosh, Samrat; Shankar, Sreejith; Philips, Divya Susan; Ajayaghosh, Ayyappanpillai

doi:10.1016/j.mtchem.2020.100242

Cited by 50 publications

(60 citation statements)

References 153 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Organic polymer photoelectric materials have received extensive attention from researchers, thanks to its broad application prospects [1][2][3][4][5][6][7][8][9][10]. For many years, scientists have studied the synthesis, structure, conductive mechanism, performance, and application of conductive polymer.…”

Section: Introductionmentioning

confidence: 99%

Electroluminescent Polymer Materials and Their Applications

Tao¹,

Li²,

Li³

et al. 2021

ACSM

View full text Add to dashboard Cite

This paper mainly introduces the light-emitting mechanism, preparation technology, and application status of electroluminescent polymer materials. As an important category of conductive polymer, electroluminescent polymer materials are also known as organic electroluminescent (EL) diode materials or organic light-emitting diode (OLED) materials. Compared with traditional display materials and devices, OLED materials boast a high light-emitting efficiency, an easily adjustable wavelength, a long service life, and an excellent machining performance. In the light of these advantages, this paper summarizes the progresses and future trends of OLED materials and devices in green lighting and panel display.

show abstract

Section: Introductionmentioning

confidence: 99%

Electroluminescent Polymer Materials and Their Applications

Tao¹,

Li²,

Li³

et al. 2021

ACSM

View full text Add to dashboard Cite

show abstract

“…[22,23] Ajayaghosh et al designed aseries of diketopyrrolopyrrole-based NIR absorption or emissiono ptoelectronic functional materials by D-A strategy. [24,25] Zhu et al reported minireviews using aq uinoline-malononitrile core as a buildingb lock for diversity-oriented synthesis of AIE luminogens (AIEgens). [26] Our group is also devoted to designing AIEgens with long wavelength emission and ah igh quantum yield in the aggregated state based on multiarylpyrroles (MAPs) as the backbone.…”

Section: Introductionmentioning

confidence: 99%

“…Ajayaghosh et al. designed a series of diketopyrrolopyrrole‐based NIR absorption or emission optoelectronic functional materials by D‐A strategy [24, 25] . Zhu et al.…”

Section: Introductionmentioning

confidence: 99%

The Aggregation Regularity Effect of Multiarylpyrroles on Their Near‐Infrared Aggregation‐Enhanced Emission Property

Ren

Shi

et al. 2020

Chemistry A European J

View full text Add to dashboard Cite

Increasing the quantum yield of near-infrared (NIR) emissive dyes is criticalf or biological applications because thesef luorescent dyes generally show decreased emission efficiency under aqueous conditions. In this work, we designed and synthesized several multiarylpyrrole (MAP) derivatives, in which af uranylidene (FE) group at the 3-position of the pyrrole forms donor-p-acceptor molecules, MAP-FE, with aN IR emissive wavelength and aggregation-enhanced emission (AEE) features. Different alkyl chains of MAP-FEs linked to phenylg roups at the 2,5-position of the pyrrole ring resulted in different emissive wavelengths and quantum yields in aggregated states, such as powders or single crystals. Powder XRD dataa nd single crystal analysis elucidated thatt he different lengths of alkyl chains had a significant impact on the regularity of MAP-FEs when they were forced to aggregate or precipitate, which affected the intermolecular interaction and the restriction degree of the rotatingp arts, which are essential components.T herefore, an increasing number of NIR dyes could be developed by this designs trategy to produce efficient NIR dyes with AEE. Moreover, this method can provide general guidance for other relatedf ields, such as organic solarc ells and organic light-emitting materials, because they are all applied in the aggregated state.

show abstract

“…They also lend themselves to tunability in terms of their optical properties. The Diketopyrrolopyrrole (DPP) family of materials has found wide-range applicability in the field of organic field-effect transistors, 9 organic solar cells, 10 organic light emitting diodes, 11 photocatalysis 12 and fluorescent sensors. 13 The photophysics of DPP based materials is on the other hand, is an active area of research owing to the flexibility in the conformational possibilities as well as their tunability from their functionalization.…”

Section: Introductionmentioning

confidence: 99%

Tuning the Formation of J and H Aggregates in Diketopyrrolopyrrole Materials

Gupta¹,

Sarkalya²,

Ganduri³

et al. 2020

Preprint

View full text Add to dashboard Cite

<div>The aggregation of molecules in devices plays a central role in determining their functional</div><div>properties. In the aggregated state, pi conjugated chromophores can exhibit enhanced emission</div><div>in comparison to their dilute solution. Here we synthesize and characterize a diketopyrrolopyrrole</div><div>(DPP) based donor-acceptor molecule in terms of its optical properties in</div><div>solution and thin film. Temperature and concentration dependent photoluminescence studies</div><div>reveal the presence of both H and J aggregates in thin film, which is corroborated by</div><div>computational investigations of the coulombic coupling in the crystal structure of the DPP</div><div>derivative. We find that the type of aggregate formed is extremely sensitive to the variation</div><div>in the shearing angle between the monomers in the crystal structure geometry.</div>

show abstract

Diketopyrrolopyrrole-based functional supramolecular polymers: next-generation materials for optoelectronic applications

Cited by 50 publications

References 153 publications

Electroluminescent Polymer Materials and Their Applications

Electroluminescent Polymer Materials and Their Applications

The Aggregation Regularity Effect of Multiarylpyrroles on Their Near‐Infrared Aggregation‐Enhanced Emission Property

Tuning the Formation of J and H Aggregates in Diketopyrrolopyrrole Materials

Contact Info

Product

Resources

About