Back to Search Start Over

Strategies for the Controlled Covalent Double Functionalization of Graphene Oxide

Authors :
Cécilia Ménard-Moyon
Shi Guo
Jésus Raya
Alberto Bianco
Isabella Anna Vacchi
Immunopathologie et chimie thérapeutique (ICT)
Institut de biologie moléculaire et cellulaire (IBMC)
Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)
Institut de Chimie de Strasbourg
Centre National de la Recherche Scientifique (CNRS)-Université Louis Pasteur - Strasbourg I-Institut de Chimie du CNRS (INC)
Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
Source :
Chemistry – A European Journal, Chemistry, Chemistry, 2020, ⟨10.1002/chem.201905785⟩
Publication Year :
2020

Abstract

Graphene oxide (GO) is a versatile platform with unique properties that have found broad applications in the biomedical field. Double functionalization is a key aspect in the design of multifunctional GO with combined imaging, targeting, and therapeutic properties. Compared to noncovalent functionalization, covalent strategies lead to GO conjugates with a higher stability in biological fluids. However, only a few double covalent functionalization approaches have been developed so far. The complexity of GO makes the derivatization of the oxygenated groups difficult to control. The combination of a nucleophilic epoxide ring opening with the derivatization of the hydroxyl groups through esterification or Williamson reaction was investigated. The conditions were selective and mild, thus preserving the structure of GO. Our strategy of double functionalization holds great potential for different applications in which the derivatization of GO with different molecules is needed, especially in the biomedical field.

Details

ISSN :
09476539 and 15213765
Database :
OpenAIRE
Journal :
Chemistry – A European Journal
Accession number :
edsair.doi.dedup.....bc89e75820e3484653b583770edb91da
Full Text :
https://doi.org/10.1002/chem.201905785