N-Heterocyclic carbene-ended polymers as surface ligands of plasmonic metal nanoparticles

被引:24
作者
Thanneeru, Srinivas [1 ]
Ayers, Kaitlynn M. [1 ]
Anuganti, Murali [1 ]
Zhang, Lei [1 ]
Kumar, Challa V. [1 ]
Ung, Gael [1 ]
He, Jie [1 ,2 ]
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Inst Mat Sci, Polymer Program, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
PROTECTED GOLD NANOPARTICLES; SELF-ASSEMBLED MONOLAYERS; COUPLING-CONSTANTS; NHC; VESICLES; FUNCTIONALIZATION; STABILIZATION; COMPLEXES; PALLADIUM; CATALYSIS;
D O I
10.1039/c9tc04776j
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A facile methodology to prepare N-heterocyclic carbene (NHC)-terminated polymers as surface ligands to functionalize gold nanoparticles (AuNPs) is reported. Our method highlights a mild, aerobic synthesis of NHC-functionalized polymers and a simple ligand exchange approach towards surface modification of AuNPs prepared in aqueous solution. Two methods, including end-group functionalization of halogen-ended polymers from a conventional atom transfer radical polymerization (ATRP) and post-polymerization functionalization of imidazole-containing polymers using imidazole-containing ATRP initiator, have been investigated to prepare imidazolium-ended polymers. Using a one-step, oxygen and moisture tolerant procedure, the polymer-NHC-Cu(i) species can be synthesized from imidazolium-ended polymers and readily bind to citrate-capped AuNPs likely through transmetalation, yielding robust polymer-stabilized AuNPs. Our synthetic method significantly simplifies the preparation and use of polymer-NHC ligands for surface functionalization of metal NPs. Our methodology is general and potentially applicable to any polymers prepared by ATRP to functionalize metal NPs via NHC-metal coordination; therefore, it will likely broaden the applications of polymer-NHC ligands for metal nanoparticles in the fields of catalysis and nanomedicine.
引用
收藏
页码:2280 / 2288
页数:9
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