Dielectric spectroscopy studies of conformational relaxation dynamics in molecular glass-forming liquids

We review experimental results obtained with broadband dielectric spectroscopy concerning the relaxation times and activation energies of intramolecular conformational relaxation processes in small-molecule glass-formers. Such processes are due to the interconversion between different conformers of...

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Detalles Bibliográficos
Autores: Romanini, Michela|||0000-0002-1685-855X, Macovez, Roberto|||0000-0001-5026-9372, Valenti, Sofia, Noor, Wahi, Tamarit Mur, José Luis|||0000-0002-7965-0000
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/403413
Acceso en línea:https://hdl.handle.net/2117/403413
https://dx.doi.org/10.3390/ijms242417189
Access Level:acceso abierto
Palabra clave:Broadband dielectric spectroscopy
Molecular rotation
Glass manufacture -- Chemistry
Molecular conformers
Secondary relaxations
Activation barrier
Characteristic relaxation time
Internal rotation
Ring buckling
Ring inversion
Rotational isomerism
Rotació molecular
Vidre -- Fabricació -- Química
Àrees temàtiques de la UPC::Física::Física molecular
Descripción
Sumario:We review experimental results obtained with broadband dielectric spectroscopy concerning the relaxation times and activation energies of intramolecular conformational relaxation processes in small-molecule glass-formers. Such processes are due to the interconversion between different conformers of relatively flexible molecules, and generally involve conformational changes of flexible chain or ring moieties, or else the rigid rotation of planar groups, such as conjugated phenyl rings. Comparative analysis of molecules possessing the same (type of) functional group is carried out in order to test the possibility of assigning the dynamic conformational isomerism of given families of organic compounds to the motion of specific molecular subunits. These range from terminal halomethyl and acetyl/acetoxy groups to both rigid and flexible ring structures, such as the planar halobenzene cycles or the buckled saccharide and diazepine rings. A short section on polyesters provides a generalisation of these findings to synthetic macromolecules.