journal article·2006-12-01

Dendron-Functionalized Superparamagnetic Nanoparticles with Switchable Solubility in Organic and Aqueous Media: Matrices for Homogeneous Catalysis and Potential MRI Contrast Agents

Chuansong Duanmu, Indrajit Saha, Yan Zheng, Boyd M. Goodson, Yong Gao

Chemistry of Materials· Volume 18· Issue 25
Publisher page

Abstract

Maghemite nanoparticles protected with a shell of Simanek (melamine) dendrons of three different generations were achieved via multiple-step syntheses. The resulting nanoclusters exhibited switchable solubility in various solvents and were examined as soluble matrices for supporting magnetically recoverable homogeneous Pd catalysts in organic solvents and as potential MRI contrast agents in aqueous media. Successful promotion of Suzuki reactions and the observation of generation-dependent dendritic effects with strong MR relaxivities suggest broad application possibilities for dendron-maghemite nanoparticles across many fields.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Dendrimers and Hyperbranched Polymers · Synthesis and Characterization of Heterocyclic Compounds · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Biochemistry, Southern Illinois University, Carbondale, Illinois 62901-4409

References (23)

Show source-provided references
1. Hagen J. · 1999
2. Cole-Hamilton D. · J. Science · 2003 · 299 · 1706
3. Zheng Y. · J. Org. Chem. · 2006 · 71 · 53710.1021/jo051861z ↗
4. Stevens P. D. · Org. Lett. · 2005 · 7 · 208510.1021/ol050218w ↗
5. Hu A. · J. Am. Chem. Soc. · 2005 · 127 · 1248610.1021/ja053881o ↗
6. For · J. Chem. Rev. · 2001 · 101 · 381910.1021/cr990116h ↗
7. Weissleder R. · Nat. Biotechnol. · 2005 · 23 · 141810.1038/nbt1159 ↗
8. Bulte J. W. M. · Nat. Biotechnol. · 2001 · 19 · 114110.1038/nbt1201-1141 ↗
9. Frank J. A. · Radiology · 2003 · 228 · 48010.1148/radiol.2281020638 ↗
10. Kalish H. · Magn. Reson. Med. · 2003 · 50 · 27510.1002/mrm.10556 ↗
11. Frank J. A. · Acad. Radiol. · 2002 · 9 · S48410.1016/S1076-6332(03)80271-4 ↗
12. Bulte J. W. M. · Magn. Reson. Med. · 1999 · 42 · 37910.1002/(SICI)1522-2594(199908)42:2<379::AID-MRM20>3.0.CO;2-L ↗
13. Bowen C. V. · Magn. Reson. Med. · 2002 · 48 · 5210.1002/mrm.10192 ↗
14. Bjornerud A. · Magn. Reson. Med. · 2002 · 47 · 46110.1002/mrm.10066 ↗
15. Morales M. P. · J. Magn. Magn. Mater. · 2003 · 266 · 10210.1016/S0304-8853(03)00461-X ↗
16. For · Mol. Pharm. · 2005 · 2 · 30210.1021/mp050019e ↗
17. The · Adv. Mater. · 2005 · 17 · 142910.1002/adma.200401991 ↗
18. Lim J. · Mol. Pharm. · 2005 · 2 · 27310.1021/mp050030e ↗
19. Zhang W. · Org. Lett. · 2000 · 2 · 84310.1021/ol005585g ↗
20. Park J. · Nat. Mater. · 2004 · 3 · 89110.1038/nmat1251 ↗
21. Some · Science · 2001 · 291 · 211510.1126/science.1057553 ↗
22. For · J. Am. Chem. Soc. · 2004 · 126 · 720610.1021/ja049195r ↗
23. For · Tetrahedron Lett. · 1979 · 20 · 343710.1016/S0040-4039(01)95429-2 ↗