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Bulky Isopropyl Group Loaded Tetraaryl Pyrene Based Azo-Linked Covalent Organic Polymer for Nitroaromatics Sensing and CO(2) Adsorption

[Image: see text] An azo-linked covalent organic polymer, Py-azo-COP, was synthesized by employing a highly blue-fluorescent pyrene derivative that is multiply substituted with bulky isopropyl groups. Py-azo-COP was investigated for its sensing and gas adsorption properties. Py-azo-COP shows selecti...

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Detalles Bibliográficos
Autores principales: Gupta, Sandeep K., Kaleeswaran, Dhananjayan, Nandi, Shyamapada, Vaidhyanathan, Ramanathan, Murugavel, Ramaswamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641411/
https://www.ncbi.nlm.nih.gov/pubmed/31457676
http://dx.doi.org/10.1021/acsomega.7b00515
Descripción
Sumario:[Image: see text] An azo-linked covalent organic polymer, Py-azo-COP, was synthesized by employing a highly blue-fluorescent pyrene derivative that is multiply substituted with bulky isopropyl groups. Py-azo-COP was investigated for its sensing and gas adsorption properties. Py-azo-COP shows selective sensing toward the electron-deficient polynitroaromatic compound picric acid among the many other competing analogs that were investigated. Apart from its chemosensing ability, Py-azo-COP (surface area 700 m(2) g(–1)) exhibits moderate selectivity toward adsorption of CO(2) and stores up to 8.5 wt % of CO(2) at 1 bar and 18.2 wt % at 15.5 bar at 273 K, although this is limited due to the electron-rich −N=N– linkages being flanked by isopropyl groups. Furthermore, the presence of a large number of isopropyl groups imparts hydrophobicity to Py-azo-COP, as confirmed by the increased adsorption of toluene compared to that of water in the pores of the COP.