journal article·2026

Sc(OTf) 3 -induced, selective removal of alkynyl ligands from heteroleptic Au 13 and Au 38 nanoclusters

Zengguang Huang, Shinjiro Takano, Tatsuya Tsukuda

Nanoscale· Volume 18· Issue 3
Publisher page

Abstract

The heteroleptic gold nanoclusters [Au13(dppe)5(PA)2]3+ (dppe = 1,2-bis(diphenylphosphino)ethane; PA- = phenylacetylide) and [Au38(PPh3)4(PA)20]2+ underwent the removal of PA- and an [Au(PA)2]- staple unit, respectively, via reaction with the Lewis acid scandium trifluoromethanesulfonate (Sc(OTf)3). The surface-exposed [Au37(PPh3)4(PA)18]3+ obtained from the Au38 nanocluster self-assembled into a dimer with two di-isocyanide linker molecules. This non-thermal strategy provides a foundation for the targeted synthesis of novel AuNCs with well-defined naked sites that can act as selective catalysts or building blocks for assembled materials.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Catalytic Cross-Coupling Reactions · Catalytic Alkyne Reactions

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

Japan Science and Technology Corporation · Japan Society for the Promotion of Science

References (45)

Show source-provided references
1. Jin · Chem. Rev. · 2016 · 116 · 1034610.1021/acs.chemrev.5b00703 ↗
2. Chakraborty · Chem. Rev. · 2017 · 117 · 820810.1021/acs.chemrev.6b00769 ↗
3. Kawawaki · Chem. – Eur. J. · 2020 · 26 · 1615010.1002/chem.202001877 ↗
4. Takano · J. Am. Chem. Soc. · 2021 · 143 · 168310.1021/jacs.0c11465 ↗
5. Zou · Chem. Soc. Rev. · 2023 · 52 · 589210.1039/D2CS00876A ↗
6. Konishi · Struct. Bonding · 2014 · 161 · 4910.1007/430_2014_143 ↗
7. Niihori · Bull. Chem. Soc. Jpn. · 2019 · 92 · 66410.1246/bcsj.20180357 ↗
8. Albright · J. Am. Chem. Soc. · 2024 · 146 · 575910.1021/jacs.3c11031 ↗
9. Yang · Adv. Mater. · 2025 · e0857810.1002/adma.202508578 ↗
10. Narouz · Nat. Chem. · 2019 · 11 · 41910.1038/s41557-019-0246-5 ↗
11. Sakamoto · ACS Catal. · 2023 · 13 · 326310.1021/acscatal.2c06197 ↗
12. Sakamoto · Nanoscale · 2024 · 16 · 2060810.1039/D4NR03385J ↗
13. Liu · J. Am. Chem. Soc. · 2017 · 139 · 212210.1021/jacs.6b10978 ↗
14. Du · Chem. Rev. · 2020 · 120 · 52610.1021/acs.chemrev.8b00726 ↗
15. Jin · Chem. Rev. · 2021 · 121 · 56710.1021/acs.chemrev.0c00495 ↗
16. Jing · Chem. Rev. · 2023 · 123 · 594810.1021/acs.chemrev.2c00569 ↗
17. Zhang · Nanoscale · 2024 · 16 · 152610.1039/D3NR05460H ↗
18. Masuda · Nanoscale · 2024 · 16 · 451410.1039/D3NR05857C ↗
19. Isozaki · ACS Catal. · 2021 · 11 · 1318010.1021/acscatal.1c03394 ↗
20. Wang · J. Am. Chem. Soc. · 2022 · 144 · 378710.1021/jacs.2c01570 ↗
21. Gao · J. Am. Chem. Soc. · 2022 · 144 · 525810.1021/jacs.2c00725 ↗
22. Guan · Angew. Chem., Int. Ed. · 2022 · 61 · e20220972510.1002/anie.202209725 ↗
23. Isozaki · Angew. Chem., Int. Ed. · 2023 · 63 · e20231213510.1002/anie.202312135 ↗
24. Zhu · J. Am. Chem. Soc. · 2024 · 146 · 2321210.1021/jacs.4c05530 ↗
25. Ueda · ACS Catal. · 2025 · 15 · 1226010.1021/acscatal.5c01743 ↗
26. Liu · J. Am. Chem. Soc. · 2025 · 147 · 2798110.1021/jacs.5c07580 ↗
27. Masuda · ACS Catal. · 2023 · 13 · 1617910.1021/acscatal.3c03323 ↗
28. Masuda · ACS Catal. · 2024 · 14 · 1712310.1021/acscatal.4c03871 ↗
29. Dong · Angew. Chem., Int. Ed. · 2025 · 64 · e20242031410.1002/anie.202420314 ↗
30. Sugiuchi · Chem. Commun. · 2015 · 51 · 1351910.1039/C5CC04312C ↗
31. Li · Sci. Adv. · 2017 · 3 · e160319310.1126/sciadv.1603193 ↗
32. Zhao · Angew. Chem., Int. Ed. · 2024 · 63 · e20231664910.1002/anie.202316649 ↗
33. Swierczewski · Angew. Chem., Int. Ed. · 2023 · 62 · e20221574610.1002/anie.202215746 ↗
34. Fukumoto · Angew. Chem., Int. Ed. · 2024 · 63 · e20240202510.1002/anie.202402025 ↗
35. Fukumoto · Nano Lett. · 2025 · 25 · 1224810.1021/acs.nanolett.5c02770 ↗
36. Kobayashi · Eur. J. Org. Chem. · 1999 · 1510.1002/(SICI)1099-0690(199901)1999:1<15::AID-EJOC15>3.0.CO;2-B ↗
37. Kumar · Asian J. Org. Chem. · 2024 · 13 · e20240029510.1002/ajoc.202400295 ↗
38. Wan · Sci. Adv. · 2017 · 3 · e170182310.1126/sciadv.1701823 ↗
39. Lei · Dalton Trans. · 2017 · 46 · 342710.1039/C6DT04763G ↗
40. Lei · Acc. Chem. Res. · 2018 · 51 · 246510.1021/acs.accounts.8b00359 ↗
41. Chen · Angew. Chem., Int. Ed. · 2020 · 59 · 754210.1002/anie.202000073 ↗
42. Wang · Science · 2023 · 381 · 78410.1126/science.adh2365 ↗
43. Saito · Coord. Chem. Rev. · 2022 · 470 · 21471310.1016/j.ccr.2022.214713 ↗
44. Yen · Inorg. Chem. · 2024 · 63 · 532010.1021/acs.inorgchem.4c00139 ↗
45. CCDC 2484462: Experimental Crystal Structure Determination , 2025 , 10.5517/ccdc.csd.cc2pd8yb10.5517/ccdc.csd.cc2pd8yb ↗