How To Make Nitroaromatic Compounds Glow: Next‐Generation Large X‐Shaped, Centrosymmetric Diketopyrrolopyrroles. (10th July 2020)
- Record Type:
- Journal Article
- Title:
- How To Make Nitroaromatic Compounds Glow: Next‐Generation Large X‐Shaped, Centrosymmetric Diketopyrrolopyrroles. (10th July 2020)
- Main Title:
- How To Make Nitroaromatic Compounds Glow: Next‐Generation Large X‐Shaped, Centrosymmetric Diketopyrrolopyrroles
- Authors:
- Skonieczny, Kamil
Papadopoulos, Ilias
Thiel, Dominik
Gutkowski, Krzysztof
Haines, Philipp
McCosker, Patrick M.
Laurent, Adèle D.
Keller, Paul A.
Clark, Timothy
Jacquemin, Denis
Guldi, Dirk M.
Gryko, Daniel T. - Abstract:
- Abstract: Red‐emissive π‐expanded diketopyrrolopyrroles (DPPs) with fluorescence reaching λ=750 nm can be easily synthesized by a three‐step strategy involving the preparation of diketopyrrolopyrrole followed by N‐arylation and subsequent intramolecular palladium‐catalyzed direct arylation. Comprehensive spectroscopic assays combined with first‐principles calculations corroborated that both N‐arylated and fused DPPs reach a locally excited (S1 ) state after excitation, followed by internal conversion to states with solvent and structural relaxation, before eventually undergoing intersystem crossing. Only the structurally relaxed state is fluorescent, with lifetimes in the range of several nanoseconds and tens of picoseconds in nonpolar and polar solvents, respectively. The lifetimes correlate with the fluorescence quantum yields, which range from 6 % to 88 % in nonpolar solvents and from 0.4 % and 3.2 % in polar solvents. A very inefficient (T1 ) population is responsible for fluorescence quantum yields as high as 88 % for the fully fused DPP in polar solvents. Abstract : Go with the glow : A two‐step process has been developed that transforms parent diketopyrrolopyrrole into structures with up to 10 fused rings. The absorptions are bathochromically shifted to the deep‐red region and strong red emission is seen, even in nonpolar solvents, despite the presence of NO2 groups.
- Is Part Of:
- Angewandte Chemie. Volume 132:Number 37(2020)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 132:Number 37(2020)
- Issue Display:
- Volume 132, Issue 37 (2020)
- Year:
- 2020
- Volume:
- 132
- Issue:
- 37
- Issue Sort Value:
- 2020-0132-0037-0000
- Page Start:
- 16238
- Page End:
- 16247
- Publication Date:
- 2020-07-10
- Subjects:
- diketopyrrolopyrroles -- donor–acceptor systems -- dyes/pigments -- fluorescence -- lactams
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202005244 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20935.xml