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Frontispiece: Luminescent Gold(III) Thiolates: Supramolecular Interactions Trigger and Control Switchable Photoemissions from Bimolecular Excited States
Author(s) -
Currie Lucy,
FernandezCestau Julio,
Rocchigiani Luca,
Bertrand Benoît,
Lancaster Simon J.,
Hughes David L.,
Duckworth Helen,
Jones Saul T. E.,
Credgington Dan,
Penfold Thomas J.,
Bochmann Manfred
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201780164
Subject(s) - stacking , supramolecular chemistry , excited state , luminescence , monomer , pyrazine , photoluminescence , chemistry , crystallography , molecule , photochemistry , picosecond , crystal structure , materials science , stereochemistry , optoelectronics , organic chemistry , polymer , physics , atomic physics , optics , laser
Luminescent Supramolecular Assemblies Gold(III) thiolates supported by pyrazine‐based C^N^C pincer ligands show a variable photoluminescent behaviour that depends strongly on the type of pyrazine π‐stacking. Different types of π‐stacking lead to crystal polymorphs, but are also present in solution. Red emissions occur from a dimeric excited state, while monomeric or weakly stacked molecules give green emissions. The image illustrates that this π‐stacking is reversible, so that the emissions can switch between red and green. For more details, see the Full Paper by Fernandez‐Cestau, Credgington, Penfold, Bochmann et al. on page 105 ff.

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