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Cyanogen isocyanate (NC–NCO) revisited: thermal and chemical reactivity of a hydrogen-free precursor to C–N–(O) polymers
Carsten Ludwig Schmidt,Martin Jansen
Journal of Materials Chemistry Pub Date : 11/06/2009 00:00:00 , DOI:10.1039/B914380G
Abstract

The first inorganic polyisocyanate, (NC–NCO)x, has been prepared and investigated. By polyaddition (polymerisation) of the reactive monomer cyanogen isocyanate (NCNCO) at low temperatures, the moisture-sensitive polymer was obtained as a phase pure solid. Using several analytical techniques (UV, IR, NMR, MS, DSC, TGA), the formation and the principal connectivity patterns of the hydrogen-free amorphous inorganic network have been settled. From the experimental results, a close structural relation to the organic “nylons” was deduced. Upon thermal impact, this inorganic macromolecule behaves like a typical thermosetting material. Exposing polymeric C2N2O to a temperature between 400 and 500 °C leads to quantitative removal of oxygen in the form of CO2. Depolymerisation and fragmentation at higher temperatures resulted in a virtually complete mass loss due to release of gaseous species. Some preliminary results concerning the high-pressure transformation towards a crystalline “C2N2O” (carbon oxynitride) are also given.

Graphical abstract: Cyanogen isocyanate (NC–NCO) revisited: thermal and chemical reactivity of a hydrogen-free precursor to C–N–(O) polymers
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