Dendritic functionalization of monolayer-protected gold nanoparticles
Source abstract
Abstract
Abstract This paper describes the facile synthesis of nanoparticle-cored dendrimers (NCDs) and nanoparticle megamers from monolayer-protected gold clusters using either single or multi-step reactions. First, 11-mercaptoundecanoic acid/hexanethiolate-protected gold clusters were synthesized using the Schiffrin reaction followed by the ligand place-exchange reaction. A convergent approach for the synthesis of nanoparticle-cored dendrimers uses a single step reaction that is an ester coupling reaction of hydroxy-functionalized dendrons with carboxylic acid-functionalized gold clusters. A divergent approach, which is based on multi-step reactions, employs the repetition of an amide coupling reaction and a Michael addition reaction to build polyamidoamine dendritic architectures around a nanoparticle core. Nanoparticle megamers, which are large dendrimer-induced nanoparticle aggregates with an average diameter of more than 300 nm, were prepared by the amide coupling reaction between polyamiodoamine [G-2] dendrimers and carboxylic acid-functionalized gold clusters. 1H NMR spectroscopy, FT-IR spectroscopy, thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) were used for the characterization of these hybrid nanoparticles.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Dendrimers and Hyperbranched Polymers · Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (25)
Show source-provided references
1. Scott · J. Phys. Chem. B · 2005 · 109 · 69210.1021/jp0469665 ↗
2. Wilson · J. Am. Chem. Soc. · 2005 · 127 · 101510.1021/ja045224m ↗
3. Narayanan · J. Phys. Chem. B · 2004 · 108 · 857210.1021/jp037169u ↗
4. Pérignon · Chem. Mater. · 2004 · 16 · 485610.1021/cm048821g ↗
5. Esumi · Langmuir · 2004 · 20 · 23710.1021/la035440t ↗
6. Rahim · Nano Lett. · 2001 · 1 · 49910.1021/nl015574w ↗
7. Kim · Chem. Commun. · 2001 · 20 · 66710.1039/b100575h ↗
8. Gopidas · J. Am. Chem. Soc. · 2003 · 125 · 649110.1021/ja029544m ↗
9. Gopidas · J. Am. Chem. Soc. · 2003 · 125 · 1416810.1021/ja036626h ↗
10. Gopidas · Nano Lett. · 2003 · 3 · 175710.1021/nl0348490 ↗
11. Wang · J. Am. Chem. Soc. · 2002 · 124 · 229310.1021/ja016711u ↗
12. Daniel · J. Am. Chem. Soc. · 2003 · 125 · 261710.1021/ja021325d ↗
13. Astruc · Chem. Commun. · 2004 · 23 · 263710.1039/b410399h ↗
14. Daniel · Chem. Rev. · 2004 · 104 · 29310.1021/cr030698+ ↗
15. Y.-S. Shon, Metal Nanoparticles Protected with Monolayers: Synthetic Methods. Dekker Encyclopedia of Nanoscience and Nanotechnology, 2004, E-ENN-120034034.10.1201/9781439834398.ch151 ↗
16. Choo · Langmuir · 2003 · 19 · 855510.1021/la035017k ↗
17. Brust · Chem. Commun. · 1994 · 13 · 80110.1039/C39940000801 ↗
18. Hostetler · Langmuir · 1998 · 14 · 1710.1021/la970588w ↗
19. Hostetler · Langmuir · 1999 · 15 · 378210.1021/la981598f ↗
20. Donkers · Langmuir · 2004 · 20 · 470310.1021/la0497494 ↗
21. Ionita · Langmuir · 2004 · 20 · 1153610.1021/la048121q ↗
22. Fréchet · 2001
23. Tomalia · High Perform. Polym. · 2001 · 13 · S110.1088/0954-0083/13/2/301 ↗
24. Tomalia · Pure Appl. Chem. · 2000 · 72 · 234310.1351/pac200072122343 ↗
25. Khopade · Macromol. Rapid Commun. · 2005 · 26 · 44510.1002/marc.200400523 ↗