Synthesis of functionalized diazocines for application as building blocks in photo- and mechanoresponsive materials.

ABSTRACT: Seven symmetrically 3,3'-substituted diazocines were synthesized. Functional groups include alcohol, azide, amine and vinyl groups, which are suitable for polymer synthesis. Upon irradiation at 385 and 530 nm the diazocines perform a reversible, pincer-type movement switching the 3,3'-distance between 6.1 Å (cis, stable isomer) and 8.2 Å (trans, metastable isomer). Key reactions in the synthesis are an oxidative C-C coupling of 2-nitrotoluenes (75-82% yield) and a reductive ring closure to form the diazocines (56-60% yield). The cyclization of the dinitro compound to the azo compound was improved in yield and reproducibility, by over-reduction to the hydrazine and reoxidation to the azo unit. In contrast to 3,3'- and 4,4'-diaminodiazocine, which have been implemented in macro

SUBMITTER: Moormann W 

PROVIDER: S-EPMC6444418 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature