Thiol-ene induced diphosphonic acid functionalization of superparamagnetic iron oxide nanoparticles

Multifunctional organic molecules represent an interesting challenge for nanoparticle functionalization due to the potential for undesirable interactions between the substrate material and the variable functionalities, making it difficult to control the final orientation of the ligand. In the presen...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 26(2010), 14 vom: 20. Juli, Seite 12285-92
1. Verfasser: Rutledge, Ryan D (VerfasserIn)
Weitere Verfasser: Warner, Cynthia L, Pittman, Jonathan W, Addleman, R Shane, Engelhard, Mark, Chouyyok, Wilaiwan, Warner, Marvin G
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Diphosphonates Ferric Compounds Ligands Sulfhydryl Compounds ferric oxide 1K09F3G675
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520 |a Multifunctional organic molecules represent an interesting challenge for nanoparticle functionalization due to the potential for undesirable interactions between the substrate material and the variable functionalities, making it difficult to control the final orientation of the ligand. In the present study, UV-induced thiol-ene click chemistry has been utilized as a means of directed functionalization of bifunctional ligands on an iron oxide nanoparticle surface. Allyl diphosphonic acid ligand was covalently deposited on the surface of thiol-presenting iron oxide nanoparticles via the formation of a UV-induced thioether. This method of thiol-ene click chemistry offers a set of reaction conditions capable of controlling the ligand deposition and circumventing the natural affinity exhibited by the phosphonic acid moiety for the iron oxide surface. These claims are supported via a multimodal characterization platform which includes thermogravimetric analysis, X-ray photoelectron spectroscopy, and metal contact analysis and are consistent with a properly oriented, highly active ligand on the nanoparticle surface. These experiments suggest thiol-ene click chemistry as both a practical and generally applicable strategy for the directed deposition of multifunctional ligands on metal oxide nanoparticle surfaces 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
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650 7 |a Ferric Compounds  |2 NLM 
650 7 |a Ligands  |2 NLM 
650 7 |a Sulfhydryl Compounds  |2 NLM 
650 7 |a ferric oxide  |2 NLM 
650 7 |a 1K09F3G675  |2 NLM 
700 1 |a Warner, Cynthia L  |e verfasserin  |4 aut 
700 1 |a Pittman, Jonathan W  |e verfasserin  |4 aut 
700 1 |a Addleman, R Shane  |e verfasserin  |4 aut 
700 1 |a Engelhard, Mark  |e verfasserin  |4 aut 
700 1 |a Chouyyok, Wilaiwan  |e verfasserin  |4 aut 
700 1 |a Warner, Marvin G  |e verfasserin  |4 aut 
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