The cathodic behaviour of poly(alkyl) and (aryl) sulfones revisited. Mechanistic and theoretical approaches
Literature Information
Jean-Francois Bergamini, Philippe Hapiot, Corinne Lagrost, Loredana Preda, Jacques Simonet, Elena Volanschi
A series of aromatic sulfones activated by 2, 3 or 4 sulfonyl groups were reduced electrochemically in aprotic media. The electrochemical behaviour is strongly directed by the nature and the number of the substituents bound to the aromatic ring. From the analyses of cyclic voltammetry experiments, the kinetics and thermodynamic parameters were evaluated for each system and a theoretical study at the B3LYP/6-31G* level was performed simultaneously to understand the reactivity of the radical anions stemmed from these aromatic sulfones.
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











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