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Functionalization of Single-Walled Carbon Nanotubes with End-Capped Polystyrene via a Single-Step Diels-Alder Cycloaddition.


ABSTRACT: A facile, single-step, [4+2] Diels-Alder cycloaddition reaction for the surface functionalization of single-walled carbon nanotubes (SWNTs) with end-capped polystyrene chains is presented. The thermal cycloaddition reaction took place at high temperature (~230 °C) without any catalyst between the sp2 network of carbon nanotubes, which acted as dienophile, and the diphenylethylene cyclobutene (DPE-CB) terminal group of the polystyrene chain. Anionic polymerization was employed for the synthesis of the polystyrene macromolecule, and successful and quantitative end-capping reaction with the DPE-CB molecule was confirmed by matrix-assisted laser desorption/ionization time of flight mass spectroscopy. Thermogravimetric analysis revealed the wt % of the grafted macromolecule on the CNT surface as well as the grafting density of the polymer chains on the SWNTs (0.027 chains nm-2). Direct evidence for the surface functionalization and the presence of thin polystyrene film was obtained by transmission electron microscopy (TEM) and by atomic force microscopy (AFM).

SUBMITTER: Stathouraki MM 

PROVIDER: S-EPMC8038725 | biostudies-literature | 2021 Apr

REPOSITORIES: biostudies-literature

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Functionalization of Single-Walled Carbon Nanotubes with End-Capped Polystyrene via a Single-Step Diels-Alder Cycloaddition.

Stathouraki Maria-Malvina MM   Pantazidis Christos C   Mygiakis Emmanouil E   Avgeropoulos Apostolos A   Sakellariou Georgios G  

Polymers 20210406 7


A facile, single-step, [4+2] Diels-Alder cycloaddition reaction for the surface functionalization of single-walled carbon nanotubes (SWNTs) with end-capped polystyrene chains is presented. The thermal cycloaddition reaction took place at high temperature (~230 °C) without any catalyst between the <i>sp</i><sup>2</sup> network of carbon nanotubes, which acted as dienophile, and the diphenylethylene cyclobutene (DPE-CB) terminal group of the polystyrene chain. Anionic polymerization was employed f  ...[more]

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