English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Plus monthly

Global: Zendy Tools annual

Global: Zendy Tools monthly

Global: Zendy Free Plan

The effect of packing on the solid state fluorescent propensities of peptidic luminophores has been investigated. A series of peptides containing 6-nitro-coumarin-3-carboxylic acid and α-aminoisobutyric acid (Aib) has been synthesized to study the structure–property relationship and stimuli responsive emission properties of the luminophores. In spite of the presence of a coumarin chromophore, peptide 2 exhibits no solid state fluorescence. The alkyl chains of Aib affect the solid state molecular packing modes and optoelectronic properties significantly. However, the fluorescence microscopy confirmed the change of blue fluorescence of peptide 3 in crystal and in amorphous states. The X-ray crystallography sheds some light on the molecular orientation, packing and the diverse degree of π–π stacking orbital overlap of adjacent coumarin chromophores of the peptide 3. Irrespective of coumarin chromophore, the peptides exhibit different packing-induced solid state emission properties varying from one peptide to another, which highlights the effect of Aib side chains.

Packing-induced solid-state fluorescence and thermochromic behavior of peptidic luminophores