Dithiocarbamates as Capping Ligands for Water-Soluble Quantum Dots
Source abstract
Abstract
We investigated the suitability of dithiocarbamate (DTC) species as capping ligands for colloidal CdSe-ZnS quantum dots (QDs). DTC ligands are generated by reacting carbon disulfide (CS(2)) with primary or secondary amines on appropriate precursor molecules. A biphasic exchange procedure efficiently replaces the existing hydrophobic capping ligands on the QD surface with the newly formed DTCs. The reaction conversion is conveniently monitored by UV-vis absorption spectroscopy. Due to their inherent water solubility and variety of side chain functional groups, we used several amino acids as precursors in this reaction/exchange procedure. The performance of DTC-ligands, as evaluated by the preservation of luminescence and colloidal stability, varied widely among amino precursors. For the best DTC-ligand and QD combinations, the quantum yield of the water-soluble QDs rivaled that of the original hydrophobic-capped QDs dispersed in organic solvents. The mean density of DTC-ligands per nanocrystal was estimated through a mass balance calculation which suggested nearly complete coverage of the available nanocrystal surface. The accessibility of the QD surface was evaluated by self-assembly of His-tagged dye-labeled proteins and peptides using fluorescence resonance energy transfer. DTC-capped QDs were also exposed to cell cultures to evaluate their stability and potential use for biological applications. In general, DTC-capped CdSe-ZnS QDs have many advantages over other water-soluble QD formulations and provide a flexible chemistry for controlling the QD surface functionalization. Despite previous literature reports of DTC-stabilized nanocrystals, this study is the first formal investigation of a biphasic exchange method for generating biocompatible core-shell QDs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011-2230
References (47)
Show source-provided references
1. Medintz I. L. · Int. J. Nanomed. · 2008 · 3 · 151
2. Xing Y. · Cancer Biomarkers · 2008 · 4 · 30710.3233/CBM-2008-4603 ↗
3. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
4. Robel I. · J. Am. Chem. Soc. · 2006 · 128 · 238510.1021/ja056494n ↗
5. McDonald S. A. · Nat. Mater. · 2005 · 4 · 13810.1038/nmat1299 ↗
6. Dabbousi B. O. · J. Phys. Chem. B · 1997 · 101 · 946310.1021/jp971091y ↗
7. Cordero S. R. · J. Phys. Chem. B · 2000 · 104 · 1213710.1021/jp001771s ↗
8. Wang Q. · J. Am. Chem. Soc. · 2007 · 129 · 638010.1021/ja071434y ↗
9. Mattoussi H. · J. Am. Chem. Soc. · 2000 · 122 · 1214210.1021/ja002535y ↗
10. Gao X. · Nat. Biotechnol. · 2004 · 22 · 96910.1038/nbt994 ↗
11. Bruchez M. · Science · 1998 · 281 · 201310.1126/science.281.5385.2013 ↗
12. Gerion D. · J. Phys. Chem. B · 2001 · 105 · 886110.1021/jp0105488 ↗
13. Dubertret B. · Science · 2002 · 298 · 175910.1126/science.1077194 ↗
14. Chan W. C. W. · Science · 1998 · 281 · 201610.1126/science.281.5385.2016 ↗
15. Oh J. K. · J. Mater. Chem. · 2010 · 20 · 843310.1039/c0jm01084g ↗
16. Pathak S. · J. Am. Chem. Soc. · 2001 · 123 · 410310.1021/ja0058334 ↗
17. Mattoussi H. · Phys. Status Solidi B · 2001 · 224 · 27710.1002/1521-3951(200103)224:1<277::AID-PSSB277>3.0.CO;2-C ↗
18. Aldana J. · J. Am. Chem. Soc. · 2001 · 123 · 884410.1021/ja016424q ↗
19. Hanaki K. · Biochem. Biophys. Res. Commun. · 2003 · 302 · 49610.1016/S0006-291X(03)00211-0 ↗
20. Koneswaran M. · Sens. Actuators, B · 2009 · 139 · 9110.1016/j.snb.2008.09.011 ↗
21. Pong B. · Langmuir · 2008 · 24 · 527010.1021/la703431j ↗
22. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
23. Chan W. C. W. · Curr. Opin. Biotechnol. · 2002 · 13 · 4010.1016/S0958-1669(02)00282-3 ↗
24. Uyeda H. T. · J. Am. Chem. Soc. · 2005 · 127 · 387010.1021/ja044031w ↗
25. Mei B. C. · Nat. Protoc. · 2009 · 4 · 41210.1038/nprot.2008.243 ↗
26. Zhu H. · Langmuir · 2008 · 24 · 866010.1021/la801254b ↗
27. Zhao Y. · J. Am. Chem. Soc. · 2005 · 127 · 732810.1021/ja050432f ↗
28. Querner C. · J. Am. Chem. Soc. · 2004 · 126 · 1157410.1021/ja047882c ↗
29. von Wrochem F. · Nat. Nano · 2010 · 5 · 61810.1038/nnano.2010.119 ↗
30. Wang J. · J. Mater. Chem. · 2008 · 18 · 327010.1039/b803618g ↗
31. Dubois F. · J. Am. Chem. Soc. · 2007 · 129 · 48210.1021/ja067742y ↗
32. Querner C. · Chem. Mater. · 2006 · 18 · 481710.1021/cm061105p ↗
33. Clapp A. R. · Nat. Protoc. · 2006 · 1 · 125810.1038/nprot.2006.184 ↗
34. Howarth M. · Nat. Methods · 2008 · 5 · 39710.1038/nmeth.1206 ↗
35. Budavari S. · 1996
36. Weast R. C. · 1977
37. Manna L. · J. Phys. Chem. B · 2005 · 109 · 618310.1021/jp0445573 ↗
38. Willard D. M. · Nano Lett. · 2001 · 1 · 46910.1021/nl015565n ↗
39. Suzuki M. · J. Am. Chem. Soc. · 2008 · 130 · 572010.1021/ja710870e ↗
40. Mattoussi H. · J. Assoc. Lab. Autom. · 2004 · 9 · 2810.1016/S1535-5535-03-00083-2 ↗
41. Clapp A. R. · J. Am. Chem. Soc. · 2004 · 126 · 30110.1021/ja037088b ↗
42. Pons T. · J. Phys. Chem. B · 2006 · 110 · 2030810.1021/jp065041h ↗
43. Su Z. · Structure · 2008 · 16 · 113810.1016/j.str.2008.03.018 ↗
44. Susumu K. · J. Am. Chem. Soc. · 2007 · 129 · 1398710.1021/ja0749744 ↗
45. Somers R. C. · Chem. Soc. Rev. · 2007 · 36 · 57910.1039/b517613c ↗
46. Derfus A. M. · Adv. Mater. · 2004 · 16 · 96110.1002/adma.200306111 ↗
47. Jaiswal J. K. · Trends Cell Biol. · 2004 · 14 · 49710.1016/j.tcb.2004.07.012 ↗