Energetic Nitrogen-Rich Polymers with a Tetrazene-Based Backbone.

Angew Chem Int Ed Engl

Univ. Lyon, Univ. Claude Bernard Lyon 1, CNRS, CNES, ArianeGroup, LHCEP, UMR 5278, Bât. Raulin, 2 rue Victor Grignard, 69622, Villeurbanne, France.

Published: January 2021

New energetic polymers were synthesized from monomers containing a trans-2-tetrazene unit. In contrast to traditional binders, such as inert hydroxytelechelic polybutadiene or glycidyl azide polymers-in which the energetic features are on the side chains-the energetic groups in the polytetrazenes are incorporated directly in the polymer backbone. Thermal analyses demonstrated that decomposition occurs at approximately 130 °C, regardless of the polymer structure. Glass-transition temperatures ranged from -34.2 to 0.2 °C and could be lowered further (to -61 °C) with the help of a new diazidotetrazene energetic plasticizer. Interestingly, hexafluoroisopropanol (HFIP) enabled complete, room-temperature depolymerization within 1 week. This depolymerization should enable the recycling of unused pyrotechnic compositions based on these new binders.

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http://dx.doi.org/10.1002/anie.202008562DOI Listing

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