| Literature DB >> 29924884 |
Antonin Desmecht1, Timothy Steenhaut1, Florence Pennetreau1, Sophie Hermans1, Olivier Riant1.
Abstract
Polyamidoamine (PAMAM) dendrimers were covalently immobilized on multi-walled carbon nanotubes (MWNT) by two "grafting to" strategies. We demonstrate the existence of non-covalent interactions between the two components but outline the superiority of our two grafting approaches, namely xanthate and click chemistry. MWNT surfaces were functionalized with activated ester and propargylic moieties prior to their reaction with PAMAM or azido-PAMAM dendrimers, respectively. The grafting of PAMAM generations 0 to 3 was evaluated with X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and transmission electron microscopy (TEM). The versatility of our hybrids was demonstrated by post-functionalization sequences involving copper alkyne-azide cycloaddition (CuAAC). We synthesized homogeneous supported iridium complexes at the extremities of the dendrimers. In addition, our materials were used as templates for the encapsulation of Pd nanoparticles (NPs), validating our nanocomposites for catalytic applications. The palladium-based catalyst was active for carbonylative coupling over five consecutive runs without loss of activity.Entities:
Keywords: PAMAM dendrimer; carbon nanotubes; catalysis; click chemistry; functionalization
Year: 2018 PMID: 29924884 DOI: 10.1002/chem.201802301
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236