Self‐assembly of chiral diketopyrrolopyrrole chromophores giving supramolecular chains in monolayers and twisted microtapes

Author:

Humphreys Joshua12ORCID,Killalea C. Elizabeth12ORCID,Pop Flavia12ORCID,Davies E. Stephen2,Siligardi Giuliano3ORCID,Amabilino David B.124ORCID

Affiliation:

1. The GSK Carbon Neutral Laboratories for Sustainable Chemistry The University of Nottingham Jubilee Campus Nottingham UK

2. School of Chemistry University of Nottingham Nottingham UK

3. Diamond Light Source, Harwell Science and Innovation Campus Didcot Oxfordshire UK

4. Institut de Ciència de Materials de Barcelona (ICMAB‐CSIC) Campus Universitari de Cerdanyola Barcelona Spain

Abstract

AbstractChiral diketopyrrolopyrroles appended with enantiomeric ethyl lactate functions through an ether linkage to the aryl backbone of the chromophore were synthesized via the Mitsunobu reaction. The molecules have good solubility and excellent optical properties, high molar absorption coefficients, and fluorescence quantum yields. Helical aggregates with circular dichroism arising from the supramolecular arrangement are seen in both solution and thin films, and the aggregates also display circularly polarized luminescence (glum ≈ ±0.1). The molecules assemble to give monolayers on graphite and precipitate from solution forming supramolecular twisted tapes hundreds of microns long.

Funder

Engineering and Physical Sciences Research Council

University of Nottingham

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

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