journal article·2020-04Open access

Gold Nanoparticles Stabilized by Molecular Fullerenols

Ken Kokubo, Mark Kristan Espejo Cabello, Nozomi Sato, Yuta Uetake, Hidehiro Sakurai

ChemNanoMat· Volume 6· Issue 4

Abstract

Abstract Polyhydroxylated fullerene derivatives (fullerenols: C60(OH)12 and C60(OH)36) exhibit excellent stabilizing matrices for gold nanoparticles. Au:C60(OH)12 and Au:C60(OH)36 form hydrophilic colloids and are well dispersed in H2O, even though C60(OH)12 itself is barely dissolved in H2O. It was estimated that C60(OH)12 forms a two‐ to three‐layered structure with 3D O−H⋅⋅⋅O hydrogen‐bonding networks, surrounding approximately 3 nm‐sized Au NPs. The thus‐prepared Au:C60(OH)n colloids exhibited a high catalytic activity toward the reduction of 4‐nitrophenol to 4‐aminophenol. The short induction period as well as kinetic and thermodynamic parameters indicated the dynamic mobility of the fullerenol matrix and the hydrophobic nature of the interface between the Au surface and the matrix.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Fullerene Chemistry and Applications · Graphene research and applications · Nanocluster Synthesis and Applications

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

Affiliations

Division of Applied Chemistry Graduate School of Engineering Osaka University 2-1 Yamadaoka Suita Osaka 565-0871 Japan

Present address: CNT-Application Research Center National Institute of Advanced Industrial Science and Technology (AIST) Central 5, 1-1-1 Higashi Tsukuba Ibaraki 305-8565 Japan

References (100+)

Show source-provided references
1.
2. 10.1016/0021-9517(89)90034-110.1016/0021-9517(89)90034-1 ↗
3. 10.1039/c1nr10201j10.1039/c1nr10201j ↗
4. 10.1039/c3ob42207k10.1039/c3ob42207k ↗
5.
6. 10.1021/acscatal.6b0338610.1021/acscatal.6b03386 ↗
7. 10.1039/C8QM00449H10.1039/C8QM00449H ↗
8.
9. 10.1002/anie.20090435910.1002/anie.200904359 ↗
10. 10.1002/ange.20090435910.1002/ange.200904359 ↗
11. 10.1021/acs.chemrev.5b0010010.1021/acs.chemrev.5b00100 ↗
12. 10.1021/acs.jpcc.5b1123210.1021/acs.jpcc.5b11232 ↗
13. 10.1021/acs.bioconjchem.7b0036810.1021/acs.bioconjchem.7b00368 ↗
14.
15. 10.1016/S0926-860X(97)00243-310.1016/S0926-860X(97)00243-3 ↗
16. 10.1126/science.125305710.1126/science.1253057 ↗
17. 10.1021/jacs.7b0536210.1021/jacs.7b05362 ↗
18. 10.1002/anie.20190906910.1002/anie.201909069 ↗
19. 10.1039/C9SC01728C10.1039/C9SC01728C ↗
20. 10.1021/acs.accounts.6b0050610.1021/acs.accounts.6b00506 ↗
21.
22. 10.1021/la047818910.1021/la0478189 ↗
23. 10.1021/ja052161e10.1021/ja052161e ↗
24. 10.1016/j.jorganchem.2006.04.05410.1016/j.jorganchem.2006.04.054 ↗
25. 10.1246/cl.2007.21210.1246/cl.2007.212 ↗
26. 10.1021/jp070791s10.1021/jp070791s ↗
27. 10.1246/cl.2007.64610.1246/cl.2007.646 ↗
28. 10.1055/s-0028-108767410.1055/s-0028-1087674 ↗
29. 10.1246/cl.2009.90810.1246/cl.2009.908 ↗
30. 10.1246/cl.2010.4610.1246/cl.2010.46 ↗
31. 10.1351/PAC-CON-09-12-0610.1351/PAC-CON-09-12-06 ↗
32. 10.1246/cl.2010.117410.1246/cl.2010.1174 ↗
33. 10.1016/j.jorganchem.2010.08.03810.1016/j.jorganchem.2010.08.038 ↗
34. 10.1016/j.tetlet.2011.03.02710.1016/j.tetlet.2011.03.027 ↗
35. Preedasuriyachai P. · Synlett · 2011 · 1121
36. 10.1016/j.molcata.2011.03.01910.1016/j.molcata.2011.03.019 ↗
37. 10.3390/molecules1703257910.3390/molecules17032579 ↗
38. 10.1246/cl.2012.63010.1246/cl.2012.630 ↗
39. 10.1071/CH1217510.1071/CH12175 ↗
40. 10.1246/cl.2012.132810.1246/cl.2012.1328 ↗
41. 10.1021/ja309606k10.1021/ja309606k ↗
42. 10.1039/c3cy00303e10.1039/c3cy00303e ↗
43. 10.1039/C5CC04432D10.1039/C5CC04432D ↗
44.
45. 10.1021/ja073559910.1021/ja0735599 ↗
46. 10.1021/ja810045y10.1021/ja810045y ↗
47. 10.3390/molecules1601014910.3390/molecules16010149 ↗
48. 10.1002/asia.20110047810.1002/asia.201100478 ↗
49. 10.1039/c2nr11727d10.1039/c2nr11727d ↗
50. 10.1021/jp307377r10.1021/jp307377r ↗
51. 10.1038/s41598-017-10165-910.1038/s41598-017-10165-9 ↗
52. 10.1021/acs.jpcc.6b0509710.1021/acs.jpcc.6b05097 ↗
53.
54. 10.1021/ja00052a01010.1021/ja00052a010 ↗
55. 10.1039/c3992000179110.1039/c39920001791 ↗
56. 10.1039/c3993000178410.1039/c39930001784 ↗
57. 10.1021/jo00093a03010.1021/jo00093a030 ↗
58. 10.1039/C3994000046310.1039/C39940000463 ↗
59. 10.1016/0040-4020(96)00104-410.1016/0040-4020(96)00104-4 ↗
60. 10.1021/jp048796210.1021/jp0487962 ↗
61. 10.1081/SCC-20006395810.1081/SCC-200063958 ↗
62. 10.1002/adfm.20050042510.1002/adfm.200500425 ↗
63. 10.1021/nn700151z10.1021/nn700151z ↗
64. 10.1016/j.tet.2008.08.05310.1016/j.tet.2008.08.053 ↗
65. 10.1002/anie.20100128010.1002/anie.201001280 ↗
66. 10.1002/ange.20100128010.1002/ange.201001280 ↗
67. 10.1007/s12274-010-0071-z10.1007/s12274-010-0071-z ↗
68. 10.1021/je100755v10.1021/je100755v ↗
69. 10.1021/jo300118h10.1021/jo300118h ↗
70. 10.1016/j.tetlet.2017.10.05410.1016/j.tetlet.2017.10.054 ↗
71. 10.3762/bjoc.15.8710.3762/bjoc.15.87 ↗
72.
73. 10.1016/j.jphotobiol.2010.09.00610.1016/j.jphotobiol.2010.09.006 ↗
74. 10.4265/bio.14.6910.4265/bio.14.69 ↗
75. 10.3109/10715762.2010.49990510.3109/10715762.2010.499905 ↗
76. 10.1007/s11010-012-1297-810.1007/s11010-012-1297-8 ↗
77. Inui S. · J. Cosmet. Sci. · 2012 · 63 · 259
78. 10.1021/acsami.6b0489510.1021/acsami.6b04895 ↗
79. 10.1021/acsnano.7b0022110.1021/acsnano.7b00221 ↗
80.
81. 10.1002/app.3220610.1002/app.32206 ↗
82. 10.1021/nn103521g10.1021/nn103521g ↗
83. 10.1021/bm200425210.1021/bm2004252 ↗
84. 10.1021/cs200317d10.1021/cs200317d ↗
85. 10.1039/c1jm12964c10.1039/c1jm12964c ↗
86. 10.1016/j.cirp.2011.03.06810.1016/j.cirp.2011.03.068 ↗
87. 10.1039/c3ta11907f10.1039/c3ta11907f ↗
88. 10.1063/1.486118410.1063/1.4861184 ↗
89. 10.1016/j.elecom.2014.07.02510.1016/j.elecom.2014.07.025 ↗
90. 10.1002/chem.20180361210.1002/chem.201803612 ↗
91. Chen M. · Langmuir · 2019 · 35
92. 10.1002/anie.20190541010.1002/anie.201905410 ↗
93. 10.1021/acs.jpcc.9b0695110.1021/acs.jpcc.9b06951 ↗
94. 10.1039/C6CP06847B10.1039/C6CP06847B ↗
95. 10.1021/cr500537t10.1021/cr500537t ↗
96.
97. 10.1016/j.jelechem.2004.07.00610.1016/j.jelechem.2004.07.006 ↗
98. 10.1021/nn101183y10.1021/nn101183y ↗
99. 10.1002/cctc.20110024210.1002/cctc.201100242 ↗
100. 10.1016/j.ijhydene.2012.01.17310.1016/j.ijhydene.2012.01.173 ↗