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Inside Cover: Triazine‐Based Sequence‐Defined Polymers with Side‐Chain Diversity and Backbone–Backbone Interaction Motifs (Angew. Chem. Int. Ed. 12/2016)
Author(s) -
Grate Jay W.,
Mo KaiFor,
Daily Michael D.
Publication year - 2016
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.201601680
Subject(s) - sequence (biology) , polymer , cover (algebra) , macromolecule , non covalent interactions , side chain , chemistry , chain (unit) , nucleophilic substitution , polymer science , polymer chemistry , materials science , hydrogen bond , molecule , organic chemistry , physics , engineering , mechanical engineering , biochemistry , astronomy
Polymer structures with sequence control will enable new macromolecules and materials with useful functions. In their Communication on page 3925 ff., J. W. Grate et al. report how they have harnessed nucleophilic aromatic substitution reactions of cyanuric chloride to develop a new architecture for sequence‐defined polymers with side‐chain diversity and noncovalent backbone–backbone interactions.