Cargando…

Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis

Multiwalled carbon nanotubes (MWCNTs) were easily and efficiently functionalised with highly cross-linked polyamines. The radical polymerisation of two bis-vinylimidazolium salts in the presence of pristine MWCNTs and azobisisobutyronitrile (AIBN) as a radical initiator led to the formation of mater...

Descripción completa

Detalles Bibliográficos
Autores principales: Campisciano, Vincenzo, Burger, René, Calabrese, Carla, Liotta, Leonarda Francesca, Lo Meo, Paolo, Gruttadauria, Michelangelo, Giacalone, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417923/
https://www.ncbi.nlm.nih.gov/pubmed/36132762
http://dx.doi.org/10.1039/d0na00291g
_version_ 1784776831948292096
author Campisciano, Vincenzo
Burger, René
Calabrese, Carla
Liotta, Leonarda Francesca
Lo Meo, Paolo
Gruttadauria, Michelangelo
Giacalone, Francesco
author_facet Campisciano, Vincenzo
Burger, René
Calabrese, Carla
Liotta, Leonarda Francesca
Lo Meo, Paolo
Gruttadauria, Michelangelo
Giacalone, Francesco
author_sort Campisciano, Vincenzo
collection PubMed
description Multiwalled carbon nanotubes (MWCNTs) were easily and efficiently functionalised with highly cross-linked polyamines. The radical polymerisation of two bis-vinylimidazolium salts in the presence of pristine MWCNTs and azobisisobutyronitrile (AIBN) as a radical initiator led to the formation of materials with a high functionalisation degree. The subsequent treatment with sodium borohydride gave rise to the reduction of imidazolium moieties with the concomitant formation of secondary and tertiary amino groups. The obtained materials were characterised by thermogravimetric analysis (TGA), elemental analysis, solid state (13)C-NMR, Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), potentiometric titration, and temperature programmed desorption of carbon dioxide (CO(2)-TPD). One of the prepared materials was tested as a heterogeneous base catalyst in C–C bond forming reactions such as the Knoevenagel condensation and Henry reaction. Furthermore, two examples concerning a sequential one-pot approach involving two consecutive reactions, namely Knoevenagel and Michael reactions, were reported.
format Online
Article
Text
id pubmed-9417923
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher RSC
record_format MEDLINE/PubMed
spelling pubmed-94179232022-09-20 Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis Campisciano, Vincenzo Burger, René Calabrese, Carla Liotta, Leonarda Francesca Lo Meo, Paolo Gruttadauria, Michelangelo Giacalone, Francesco Nanoscale Adv Chemistry Multiwalled carbon nanotubes (MWCNTs) were easily and efficiently functionalised with highly cross-linked polyamines. The radical polymerisation of two bis-vinylimidazolium salts in the presence of pristine MWCNTs and azobisisobutyronitrile (AIBN) as a radical initiator led to the formation of materials with a high functionalisation degree. The subsequent treatment with sodium borohydride gave rise to the reduction of imidazolium moieties with the concomitant formation of secondary and tertiary amino groups. The obtained materials were characterised by thermogravimetric analysis (TGA), elemental analysis, solid state (13)C-NMR, Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), potentiometric titration, and temperature programmed desorption of carbon dioxide (CO(2)-TPD). One of the prepared materials was tested as a heterogeneous base catalyst in C–C bond forming reactions such as the Knoevenagel condensation and Henry reaction. Furthermore, two examples concerning a sequential one-pot approach involving two consecutive reactions, namely Knoevenagel and Michael reactions, were reported. RSC 2020-07-14 /pmc/articles/PMC9417923/ /pubmed/36132762 http://dx.doi.org/10.1039/d0na00291g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Campisciano, Vincenzo
Burger, René
Calabrese, Carla
Liotta, Leonarda Francesca
Lo Meo, Paolo
Gruttadauria, Michelangelo
Giacalone, Francesco
Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title_full Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title_fullStr Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title_full_unstemmed Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title_short Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
title_sort straightforward preparation of highly loaded mwcnt–polyamine hybrids and their application in catalysis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417923/
https://www.ncbi.nlm.nih.gov/pubmed/36132762
http://dx.doi.org/10.1039/d0na00291g
work_keys_str_mv AT campiscianovincenzo straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT burgerrene straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT calabresecarla straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT liottaleonardafrancesca straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT lomeopaolo straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT gruttadauriamichelangelo straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis
AT giacalonefrancesco straightforwardpreparationofhighlyloadedmwcntpolyaminehybridsandtheirapplicationincatalysis