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Entropy-Driven Selectivity for Chain Scission: Where Macromolecules Cleave

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Authors

Pahnke, Kai
Brandt, Josef
Gryn'ova, Ganna
Lin, Ching Y
Altintas, Ozcan
Schmidt, Friedrich G
Lederer, Albena
Coote, Michelle
Barner-Kowollik, Christopher

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Publisher

Wiley

Abstract

We show that, all other conditions being equal, bond cleavage in the middle of molecules is entropically much more favored than bond cleavage at the end. Multiple experimental and theoretical approaches have been used to study the selectivity for bond cleavage or dissociation in the middle versus the end of both covalent and supramolecular adducts and the extensive implications for other fields of chemistry including, e.g., chain transfer, polymer degradation, and control agent addition are discussed. The observed effects, which are a consequence of the underlying entropic factors, were predicted on the basis of simple theoretical models and demonstrated via high-temperature (HT) NMR spectroscopy of self-assembled supramolecular diblock systems as well as temperature-dependent size-exclusion chromatography (TD SEC) of covalently bonded Diels-Alder step-growth polymers.

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Citation

Source

Angewandte Chemie (International ed. in English)

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Access Statement

Open Access

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