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Frontispiece: Thermally Adjustable Dynamic Disulfide Linkages Mediated by Highly Air‐Stable 2,2,6,6‐Tetramethylpiperidine‐1‐sulfanyl (TEMPS) Radicals
Author(s) -
Takahashi Akira,
Goseki Raita,
Otsuka Hideyuki
Publication year - 2017
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201780861
Subject(s) - sulfanyl , homolysis , radical , dissociation (chemistry) , covalent bond , disulfide bond , chemistry , dynamic covalent chemistry , photochemistry , polymer , polymer chemistry , stereochemistry , organic chemistry , molecule , biochemistry , supramolecular chemistry
Polymers The dynamic covalent chemistry of 2,2,6,6‐tetramethylpiperidine‐1‐sulfanyl dimers derived from the thermally reversible homolytic dissociation of disulfide linkages is described by H. Otsuka et al. in their Communication on page 2016 ff.