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Monolayer Exchange Chemistry of γ-Fe<sub>2</sub>O<sub>3</sub> Nanoparticles

Andrew K. Boal,Kanad Das,Mark Gray,Vincent M. Rotello-2002-05-16-Chemistry of Materials
108

TL;DRAbstract

Monolayer modification of alkylamine-protected γ-Fe2O3 nanoparticles using functionalized alcohols and diols is presented. the stability of the modified nanoparticles was found to be dependent on the nature of the introduced alcohol: both bidentate surface−ligand bonding and steric blocking by bulky tail groups were necessary to produce systems resistant to agglomeration. EPR, UV−vis, and powder XRD analyses of the pre- and post-modified nanoparticles demonstrated that the core γ-Fe2O3 functionality was unaffected by the change in monolayer composition. Finally, multiple ligands could be readily incorporated into the monolayer using a simultaneous displacement reaction.

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Monolayer modification of alkylamine-protected γ-Fe2O3 nanoparticles using functionalized alcohols and diols is presented. the stability of the modified nanoparticles was found to be dependent on the nature of the introduced alcohol: both bidentate surface−ligand bonding and steric blocking by bulky tail groups were necessary to produce systems resistant to agglomeration. EPR, UV−vis, and powder XRD analyses of the pre- and post-modified nanoparticles demonstrated that the core γ-Fe2O3 functionality was unaffected by the change in monolayer composition. Finally, multiple ligands could be readily incorporated into the monolayer using a simultaneous displacement reaction.

Keywords

MonolayerNanoparticleSteric effectsChemistryLigand (biochemistry)Electron paramagnetic resonanceDenticitySingle displacement reaction

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