2022
DOI: 10.1007/s10853-021-06602-w
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A systematic review on 1,8-naphthalimide derivatives as emissive materials in organic light-emitting diodes

Abstract: Organic light-emitting devices (OLEDs) have garnered significant research attention owing to their immense application prospects in leading technologies for full-color flat panel displays and eco-friendly solid-state lighting. They demonstrate exceptional features such as mercury-free construction, wide viewing angle, superior color quality and captivating flexibility. The requirements of light-emitting organic materials pertaining to high stability, lifetime and luminescence quantum yield, combined with the f… Show more

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Cited by 40 publications
(34 citation statements)
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“…Distillation (340 C, 1-3 torr) provided a crude product (225 g, 81.6%); recrystallization (EtOH) yielded 2 as colorless platelets (192 g, 60%). 1 H NMR (500 MHz, 25 C, CDCl 3 ; d, ppm): 7.45 (d, J ¼ 8.5 Hz, 4H), 7.01 (d, J ¼ 8.5 Hz, 4H), 3.68 (s, 4H).…”
Section: 3-bis(p-bromophenyl)-2-propanone (2)mentioning
confidence: 99%
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“…Distillation (340 C, 1-3 torr) provided a crude product (225 g, 81.6%); recrystallization (EtOH) yielded 2 as colorless platelets (192 g, 60%). 1 H NMR (500 MHz, 25 C, CDCl 3 ; d, ppm): 7.45 (d, J ¼ 8.5 Hz, 4H), 7.01 (d, J ¼ 8.5 Hz, 4H), 3.68 (s, 4H).…”
Section: 3-bis(p-bromophenyl)-2-propanone (2)mentioning
confidence: 99%
“…Aer cooling to room temperature over 3 h, the dark red crystals were ltered off, washed with MeOH, and dried in vacuo (0.995 g, 74%). 1…”
Section: 3-bis(p-bromophenyl)-2-propanone (2)mentioning
confidence: 99%
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“…In literature, Supramolecular self‐assembly is being explored to design functional material for NACs because large surface‐to‐volume ratio and the effective π‐π stacking between these molecules provides ordered molecular organization which enables long‐range exciton migration and their quick annihilation by explosive quencher [24] . In this context, 1,8‐naphthalimide derivatives which have strong tendency to form intermolecular π‐π stacking to control photophysical properties, and possibility of synthetic modifications either on the naphthalene ring or at the N‐imide position with different functional group emerged as promising scaffold [25–28] . The 1,8‐naphthalimide derivatives have absorbance and fluorescence maxima in the visible and red region, high fluorescence quantum yield, good cell permeability properties which are suitable for practical application in biological system and presence of electron withdrawing imide group with planar structure facilitate intramolecular charge transfer in solution [25] .…”
Section: Introductionmentioning
confidence: 99%
“…[24] In this context, 1,8naphthalimide derivatives which have strong tendency to form intermolecular π-π stacking to control photophysical properties, and possibility of synthetic modifications either on the naphthalene ring or at the N-imide position with different functional group emerged as promising scaffold. [25][26][27][28] The 1,8naphthalimide derivatives have absorbance and fluorescence maxima in the visible and red region, high fluorescence quantum yield, good cell permeability properties which are suitable for practical application in biological system and presence of electron withdrawing imide group with planar structure facilitate intramolecular charge transfer in solution. [25] Moreover, strong intermolecular H-type π-π stacking interaction of planar unsubstituted 1,8-naphthalimide core result in the formation of excimers.…”
Section: Introductionmentioning
confidence: 99%