Perylene Monolayer Protected Gold Nanorods: Unique Optical, Electronic Properties and Self-Assemblies
Source abstract
Abstract
Here we report the synthesis and characterization of organosoluble perylene monolayer protected gold nanorods. From 1 H NMR, FT-IR, and differential scanning calorimetry experiments, the successful thiol exchange and stacking of perylene molecules on gold nanorods were confirmed. The resulting gold nanorods encapsulated with perylene thiol molecules via strong covalent Au–S linkages showed unique optical and electronic properties compared to the initial free perylene molecules and gold nanorods, indicating there were strong interactions between perylene chromophores and gold nanorods. When attached on gold nanorods, the perylene chromophores did not exhibit any typical UV–vis absorption or fluorescence emission signal, originating from the charge transfer from gold nanorods to perylene chromophores. However, the missing signals reappeared upon the addition of iodine, which detached the perylene molecules from gold nanorods. For the hybrid gold nanorods, particular electronic properties were also investigated by cyclic voltammetry and electron diffraction. Furthermore, with strong π–π intermolecular interactions, the perylene thiol monolayer protected gold nanorods were able to aggregate. When drying from highly diluted solution, gold nanorods formed well-organized side-by-side self-assembly arrays.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Liquid Crystal Institute, Kent State University, Kent, Ohio 44242, United States
Department of Chemistry, Mugla University, Mugla 48121, Turkey
Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, Ohio 44106, United States
Materials and Manufacturing Directorate, Air Force Research Laboratory WPAFB, Ohio 45433, United States
References (66)
Show source-provided references
1. Walter M. · Proc. Natl. Acad. Sci. U.S.A. · 2008 · 105 · 915710.1073/pnas.0801001105 ↗
2. Sau T. K. · Langmuir · 2005 · 21 · 292310.1021/la047488s ↗
3. Daniel M. C. · Chem. Rev. · 2004 · 104 · 29310.1021/cr030698+ ↗
4. Sun Y. G. · Science · 2002 · 298 · 217610.1126/science.1077229 ↗
5. Murphy C. J. · J. Phys. Chem. B · 2005 · 109 · 1385710.1021/jp0516846 ↗
6. Sudeep P. K. · J. Am. Chem. Soc. · 2005 · 127 · 651610.1021/ja051145e ↗
7. Huang X. H. · J. Am. Chem. Soc. · 2006 · 128 · 211510.1021/ja057254a ↗
8. Ding H. · J. Phys. Chem. C · 2007 · 111 · 1255210.1021/jp0733419 ↗
9. Sau T. K. · Langmuir · 2004 · 20 · 641410.1021/la049463z ↗
10. Khanal B. P. · Angew. Chem., Int. Ed. · 2007 · 46 · 219510.1002/anie.200604889 ↗
11. Dai Q. · Chem. Commun. · 2008 · 285810.1039/b804797a ↗
12. Li Y. N. · Langmuir · 2011 · 27 · 9810.1021/la104131y ↗
13. El Khoury J. M. · Chem. Commun. · 2009 · 210910.1039/b901826c ↗
14. Schmidt-Mende L. · Science · 2001 · 293 · 111910.1126/science.293.5532.1119 ↗
15. Hains A. W. · Chem. Rev. · 2010 · 110 · 668910.1021/cr9002984 ↗
16. Tang M. L. · J. Am. Chem. Soc. · 2009 · 131 · 373310.1021/ja809045s ↗
17. Chen Z. · Chem. Soc. Rev. · 2009 · 38 · 56410.1039/B809359H ↗
18. Anger P. · Phys. Rev. Lett. · 2006 · 96 · 410.1103/PhysRevLett.96.113002 ↗
19. Cannone F. · J. Phys. Chem. B · 2006 · 110 · 1649110.1021/jp0625816 ↗
20. Hasobe T. · J. Am. Chem. Soc. · 2005 · 127 · 121610.1021/ja047768u ↗
21. Santosh G. · J. Phys. Chem. B · 2010 · 114 · 1438910.1021/jp100662b ↗
22. Kotiaho A · J. Phys. Chem. C · 2010 · 114 · 16210.1021/jp9087173 ↗
23. Xue C · Langmuir · 2012 · 28 · 595610.1021/la300096n ↗
24. Huang Y. · Science · 2001 · 291 · 63010.1126/science.291.5504.630 ↗
25. Boal A. K. · Nature · 2000 · 404 · 74610.1038/35008037 ↗
26. Tang Z. Y. · Science · 2006 · 314 · 27410.1126/science.1128045 ↗
27. Sau T. K. · J. Am. Chem. Soc. · 2004 · 126 · 864810.1021/ja047846d ↗
28. Würthner F. · Chem. Commun. · 2004 · 156410.1039/B401630K ↗
29. Wang W. · J. Am. Chem. Soc. · 2006 · 128 · 1115010.1021/ja061826p ↗
30. Balakrishnan K. · J. Am. Chem. Soc. · 2005 · 127 · 1049610.1021/ja052940v ↗
31. Brust M. · J. Chem. Soc. Chem. Commun. · 1994 · 80110.1039/C39940000801 ↗
32. Zhou X. · J. Colloid Interface Sci. · 2007 · 308 · 38110.1016/j.jcis.2007.01.040 ↗
33. Santosh G. · J. Phys. Chem. B · 2010 · 114 · 1438910.1021/jp100662b ↗
34. Haas U. · J. Mater. Chem. · 2003 · 13 · 76710.1039/b210423g ↗
35. Christopher Love J. · Chem. Rev. · 2005 · 105 · 110310.1021/cr0300789 ↗
36. Kelber J. · Eur. J. Org. Chem. · 2011 · 70710.1002/ejoc.201001346 ↗
37. Morton S. M. · Chem. Rev. · 2011 · 111 · 396210.1021/cr100265f ↗
38. Ulman A. · Chem. Rev. · 1996 · 96 · 153310.1021/cr9502357 ↗
39. N. V. Venkataraman S. V. · J. Phys. Chem. B · 2001 · 105 · 180510.1021/jp002505h ↗
40. Xu Y. J. · Angew. Chem., Int. Ed. · 2007 · 46 · 389610.1002/anie.200604607 ↗
41. Badia A. · Chem.—Eur. J. · 1996 · 2 · 35910.1002/chem.19960020318 ↗
42. Song Y. · Langmuir · 2005 · 21 · 549210.1021/la0503606 ↗
43. Hostetler M. J. · Langmuir · 1998 · 14 · 1710.1021/la970588w ↗
44. Donkers R. L. · Langmuir · 2004 · 20 · 194510.1021/la035706w ↗
45. Schaaff T. G. · J. Phys. Chem. B · 2001 · 105 · 878510.1021/jp011122w ↗
46. Kohlmann O. · J. Phys. Chem. B · 2001 · 105 · 880110.1021/jp011123o ↗
47. Terrill R. H. · J. Am. Chem. Soc. · 1995 · 117 · 1253710.1021/ja00155a017 ↗
48. Arnaud A. · Angew. Chem., Int. Ed. · 2004 · 43 · 171810.1002/anie.200353434 ↗
49. Wang W. · Nano Lett. · 2003 · 3 · 45510.1021/nl025976j ↗
50. Ruhoff P. T. · Int. J. Quantum Chem. · 2000 · 77 · 38310.1002/(SICI)1097-461X(2000)77:1<383::AID-QUA38>3.0.CO;2-0 ↗
51. Link S. · J. Phys. Chem. B · 1999 · 103 · 841010.1021/jp9917648 ↗
52. Vukovic S. · J. Phys. Chem. C · 2009 · 113 · 12110.1021/jp808116y ↗
53. Yagai S. · Angew. Chem., Int. Ed. · 2008 · 47 · 336710.1002/anie.200705385 ↗
54. Lee D. · J. Am. Chem. Soc. · 2004 · 126 · 619310.1021/ja049605b ↗
55. Guo R. · J. Am. Chem. Soc. · 2005 · 127 · 1214010.1021/ja053119m ↗
56. Zhu M. · J. Am. Chem. Soc. · 2008 · 130 · 588310.1021/ja801173r ↗
57. Negishi Y. · J. Am. Chem. Soc. · 2005 · 127 · 526110.1021/ja042218h ↗
58. Peng Q. · J. Phys. Chem. B · 2008 · 112 · 280110.1021/jp7105428 ↗
59. Xue C. M. · Polymer · 2008 · 49 · 531410.1016/j.polymer.2008.09.040 ↗
60. Maier S. A. · Nat. Mater. · 2003 · 2 · 22910.1038/nmat852 ↗
61. Maier S. A. · Adv. Mater. · 2001 · 13 · 150110.1002/1521-4095(200110)13:19<1501::AID-ADMA1501>3.0.CO;2-Z ↗
62. Gole A. · Chem. Mater. · 2005 · 17 · 132510.1021/cm048297d ↗
63. Park H. S. · Langmuir · 2008 · 24 · 1383310.1021/la803363m ↗
64. Mitamura K. · J. Phys. Chem. B · 2007 · 111 · 889110.1021/jp072524s ↗
65. Nakashima H. · Langmuir · 2008 · 24 · 565410.1021/la8003189 ↗
66. Sreeprasad T. S. · Langmuir · 2011 · 27 · 338110.1021/la104828e ↗