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Solid‐state nuclear magnetic resonance study of polymorphism in tris(8‐hydroxyquinolinate)aluminium
Author(s) -
Cross Callum,
Cervini Luca,
Halcovitch Nathan R.,
Griffin John M.
Publication year - 2021
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.5147
Subject(s) - chemistry , aluminium , density functional theory , tris , solid state nuclear magnetic resonance , amorphous solid , dispersion (optics) , crystallography , computational chemistry , molecular physics , nuclear magnetic resonance , organic chemistry , optics , physics , biochemistry
Tris(8‐hydroxyquinolinate)aluminium (Alq 3 ) is a metal–organic coordination complex, which is a widely used electroluminescent material in organic light‐emitting diode technology. Crystalline Alq 3 is known to occur in five polymorphic forms (denoted α, β, γ, δ, and ε), although the structures of some of these polymorphs have been the subject of considerable debate. In particular, the structure of α‐Alq 3 , which is a model for the local structure in amorphous films used in devices, is highly complex and has never been conclusively solved. In this work, we use solid‐state nuclear magnetic resonance (NMR) and density functional theory (DFT) calculations to investigate the local structure of four Alq 3 samples. We find that the first structure proposed for α‐Alq 3 is inconsistent with all of the samples studied, and DFT calculations further suggest that this structure is energetically unfavourable. Instead, samples containing the meridional ( mer ) isomeric form are found to contain local structures consistent with ε‐Alq 3 , and a sample containing the facial ( fac ) isomeric form is consistent with a mixture of γ‐Alq 3 and δ‐Alq 3 . We also investigate the influence of different strategies for dispersion correction in DFT geometry optimisations. We find that a recently proposed modified semiempirical dispersion correction scheme gives good agreement with experiment. Furthermore, the DFT calculations also show that distinction between mer and fac isomers on the basis of η Q that has been assumed in previous work is not always justified.