journal article·2026

Effects of phosphine ligand denticity on catalytic activity and durability of gold nanoparticles in the oxidation of benzyl alcohol

Yiwei Wu, Shinya Masuda, Kosuke Sakamoto, Haru Hirai, Shinjiro Takano, Tatsuya Tsukuda

Nanoscale· Volume 18· Issue 5
Publisher page

Abstract

A key challenge in developing metal nanoparticle (NP) catalysts is to overcome the trade-off between the catalytic activity and resistance to aggregation. In this study, we prepared monodisperse gold NPs (diameter = 2-3 nm) protected by phosphine ligands with different denticities: triphenylphosphine (TPP), 1,2-bis(diphenylphosphino)ethane (DPPE), and tris(2-(diphenylphosphino)ethyl)phosphine (TDEP). We then investigated how the ligand denticity affects the catalytic activity and durability in the aerobic oxidation of benzyl alcohol (BnOH). The AuNPs adsorbed on the Cs2CO3 powder, which is required for deprotonating BnOH, acted as heterogeneous catalysts in 1,2-dichloroethane at 60 °C. Of the three AuNP catalysts, the TDEP-protected AuNPs exhibited the greatest activity per exposed Au atoms and the longest lifetime. Conversely, the DPPE- and TPP-protected AuNPs exhibited poorer performance in terms of activity and durability, respectively. This work provides a rational ligand design strategy that balances the activity and durability of metal NPs.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Catalytic Processes in Materials Science · Gold and Silver Nanoparticles Synthesis and Applications · Nanoporous metals and alloys

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

Affiliations

Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Funding

Core Research for Evolutional Science and Technology · Ministry of Education, Culture, Sports, Science and Technology · Japan Society for the Promotion of Science

References (47)

Show source-provided references
1. Zahmakiran · Nanoscale · 2011 · 3 · 346210.1039/c1nr10201j ↗
2. Hervés · Chem. Soc. Rev. · 2012 · 41 · 557710.1039/c2cs35029g ↗
3. An · ChemCatChem · 2012 · 4 · 151210.1002/cctc.201200229 ↗
4. Ramezani-Dakhel · Phys. Chem. Chem. Phys. · 2013 · 15 · 548810.1039/c3cp00135k ↗
5. Viñes · Chem. Soc. Rev. · 2014 · 43 · 492210.1039/C3CS60421G ↗
6. Ishida · Chem. Rec. · 2016 · 16 · 227810.1002/tcr.201600046 ↗
7. Gao · Chem. Rev. · 2020 · 121 · 83410.1021/acs.chemrev.0c00237 ↗
8. Astruc · Chem. Rev. · 2020 · 120 · 46110.1021/acs.chemrev.8b00696 ↗
9. Ishida · Chem. Rev. · 2020 · 120 · 46410.1021/acs.chemrev.9b00551 ↗
10. Sápi · Catal. Lett. · 2021 · 151 · 215310.1007/s10562-020-03477-5 ↗
11. Dimitratos · Nat. Rev. Chem. · 2024 · 8 · 19510.1038/s41570-024-00578-2 ↗
12. Qiu · Nano Lett. · 2019 · 19 · 670310.1021/acs.nanolett.9b03167 ↗
13. Peng · ACS Cent. Sci. · 2021 · 7 · 26210.1021/acscentsci.0c01486 ↗
14. Hoang · Chem. Commun. · 2022 · 58 · 972810.1039/D2CC03603G ↗
15. Guan · Angew. Chem., Int. Ed. · 2022 · 61 · e20220972510.1002/anie.202209725 ↗
16. Luo · ChemPhysChem · 2024 · 25 · e20230071510.1002/cphc.202300715 ↗
17. Gupta · Adv. Funct. Mater. · 2025 · 35 · 250704710.1002/adfm.202507047 ↗
18. Gibson · Chem. Soc. Rev. · 2013 · 42 · 720410.1039/C3CS60035A ↗
19. Gambinossi · Adv. Colloid Interface Sci. · 2015 · 222 · 33210.1016/j.cis.2014.07.015 ↗
20. Yonezawa · New J. Chem. · 1998 · 22 · 117910.1039/a805753b ↗
21. Crooks · Acc. Chem. Res. · 2001 · 34 · 18110.1021/ar000110a ↗
22. Narayaran · J. Phys. Chem. B · 2005 · 109 · 1266310.1021/jp051066p ↗
23. Yamamoto · Chem. Rev. · 2020 · 120 · 139710.1021/acs.chemrev.9b00188 ↗
24. Hasegawa · Bull. Chem. Soc. Jpn. · 2021 · 94 · 103610.1246/bcsj.20200377 ↗
25. Comeau · Langmuir · 2012 · 28 · 37710.1021/la202895n ↗
26. Chew · J. Phys. Chem. C · 2018 · 122 · 2628810.1021/acs.jpcc.8b09323 ↗
27. Sufyan · Chem. – Eur. J. · 2022 · 28 · e20220287710.1002/chem.202202877 ↗
28. Adnan · Adv. Sci. · 2022 · 9 · 210569210.1002/advs.202105692 ↗
29. Wu · Chin. Chem. Lett. · 2013 · 24 · 45710.1016/j.cclet.2013.03.054 ↗
30. Zhao · Adv. Energy Mater. · 2018 · 8 · 180140010.1002/aenm.201801400 ↗
31. Yuan · Angew. Chem., Int. Ed. · 2021 · 60 · 522510.1002/anie.202012499 ↗
32. Dong · Angew. Chem., Int. Ed. · 2025 · 64 · e20242031410.1002/anie.202420314 ↗
33. Man · J. Am. Chem. Soc. · 2018 · 140 · 157610.1021/jacs.7b08516 ↗
34. Nosratabad · Chem. Mater. · 2021 · 33 · 92110.1021/acs.chemmater.0c03918 ↗
35. Amirsardari · Chem. Pap. · 2020 · 74 · 323310.1007/s11696-020-01148-8 ↗
36. Strasser · ChemElectroChem · 2021 · 8 · 254510.1002/celc.202100549 ↗
37. Chaiseeda · ACS Omega · 2017 · 2 · 706610.1021/acsomega.7b01248 ↗
38. McKenzie · J. Am. Chem. Soc. · 2014 · 136 · 1342610.1021/ja5075689 ↗
39. Huang · Adv. Funct. Mater. · 2007 · 17 · 196610.1002/adfm.200700051 ↗
40. Chen · Appl. Phys. Lett. · 2005 · 87 · 1
41. Li · Appl. Phys. Lett. · 2006 · 88 · 25350310.1063/1.2212270 ↗
42. Lu · Adv. Funct. Mater. · 2012 · 22 · 14410.1002/adfm.201101892 ↗
43. Karimi · Chem. Commun. · 2009 · 37 · 555510.1039/b908964k ↗
44. Xia · Nat. Commun. · 2024 · 15 · 85110.1038/s41467-024-45066-9 ↗
45. Haider · Catal. Lett. · 2008 · 125 · 16910.1007/s10562-008-9567-5 ↗
46. Tsunoyama · J. Am. Chem. Soc. · 2009 · 131 · 708610.1021/ja810045y ↗
47. Hasegawa · JACS Au · 2021 · 1 · 66010.1021/jacsau.1c00102 ↗