| Literature DB >> 27572117 |
Romain Aufaure1, Julie Hardouin2, Nadine Millot3, Laurence Motte1, Yoann Lalatonne4,5, Erwann Guénin6.
Abstract
Inverse electron demand Diels-Alder (iEDDA) was evaluated for the functionalization of gold nanoparticles. The reaction was first modelled with the free coating molecule 1-hydroxy-1,1-methylenebisphosphonate bearing an alkene functionality (HMBPene). A model tetrazine 3,6-dipyridin-2-yl-1,2,4,5-tetrazine (pyTz) was used, kinetic of the reaction was calculated and coupling products were analysed by NMR and HRMS. The reaction was then transposed at the nanoparticle surface. Gold nanoparticles bearing an alkene functionality were obtained using a one-pot methodology with HMBPene and the tetrazine click chemistry was evaluated at their surface using pyTz. The successful coupling was assessed by XPS measurements. This click-methodology was extended to the conjugation of a NIR probe at the NP surface.Entities:
Keywords: bisphosphonate; click chemistry; gold; inverse electron demand Diels-Alder; nanoparticles
Year: 2016 PMID: 27572117 DOI: 10.1002/chem.201602899
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236