2008
DOI: 10.1002/ejic.200800227
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Functionalization of Gold Nanoparticles by Iron(III) Complexes Derived from Schiff Base Ligands

Abstract: A series of iron(III) complexes derived from a variety of pentadentate Schiff base ligands, namely salten [H2salten = bis(3‐salicylideneaminopropyl)amine] derivatives, have been synthesized and further used to stabilize and functionalize gold nanoparticles (Au‐NPs). The iron complexes have been specifically designed to interact with the Au‐NPs through an ambidentate thiocyanate ligand or through a pendant thiol group carried by the salten derivative ligand. The gold nanocomposites have been synthesized either … Show more

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Cited by 22 publications
(19 citation statements)
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“…In the past four years, we have studied the direct synthesis of gold NPs coated by metallic complexes [25][26][27]. The interaction between the metallic complexes and the surface was not ensured by the conventional thiol function but by the nitrogen atom(s) of pyridine, 1,10-phenanthroline (phen) and more recently thiocyanate pendant groups [28]. Moreover, the usual long alkyl chain was replaced by a fully conjugated system between the metallic NPs and the metallic center in the complex.…”
Section: Introductionmentioning
confidence: 99%
“…In the past four years, we have studied the direct synthesis of gold NPs coated by metallic complexes [25][26][27]. The interaction between the metallic complexes and the surface was not ensured by the conventional thiol function but by the nitrogen atom(s) of pyridine, 1,10-phenanthroline (phen) and more recently thiocyanate pendant groups [28]. Moreover, the usual long alkyl chain was replaced by a fully conjugated system between the metallic NPs and the metallic center in the complex.…”
Section: Introductionmentioning
confidence: 99%
“…The second approach is based on the use of a charged complex. Stabilization of the particles is done by electrostatic repulsion [196].…”
Section: Carboxylates and Base Shiff Coordination Complexesmentioning
confidence: 99%
“…In some cases, tight chemisorption of proteins on Au NPs can originate from the binding of thiol groups from cysteine residues present in the proteins (e.g., serum albumin) to the Au surface. If no thiolated residues are available in the native proteins, thiol groups can be incorporated by chemical means, for example, with 2-iminothiolane or through genetic engineering [24][25][26][27]. Some proteins and enzymes preserve their native structures and activities when they are physically adsorbed on nanoparticles.…”
Section: Functionalization Of Nanoparticles With Biomolecules By Chemmentioning
confidence: 99%