journal article·2026-04-15Open access

A Straightforward Access to Sustainable and Reusable Melanin-Supported Palladium Catalysts: Characterization and Application in Sonogashira Cross-Coupling Reactions

Simone Potenti, Pasquale Lioniello, Elisabetta Mazzotta, Nicoletta Ditaranto, Evelina Liarou, Noah Al-Shamery, Pooi See Lee, Teresa Sibillano, Cinzia Giannini, Cosimino Malitesta, Paola Manini

ACS Applied Materials & Interfaces· Volume 18· Issue 14

Abstract

In the last decades, the impact of the emergent concept of sustainable development has driven the impressive evolution of catalytic methodologies, also stimulated by the breakthrough of new materials and nanotechnologies. Based on this evidence, we report herein the design of sustainable catalysts by addressing the unexploited potential of melanin, a class of pigments widely diffused in nature. By pursuing a straightforward and sustainable approach, we prepared a series of Pd@melanin hybrids inspired from mammalian eumelanin and fungal allomelanin. XPS analyses revealed that DHImel (DHI: 5,6-dihydroxyindole) can support palladium by promoting the reduction of Pd(II) to Pd(0) thanks to the catechol groups that can be converted into quinones. HR-TEM and XRD analyses revealed that palladium atoms are uniformly distributed, forming nanoaggregates in the face-centered cubic crystal structure with an average dimension of 8 nm. The catalytic activity of the hybrids was tested in the Sonogashira cross-coupling reaction. Overall, the collected data suggested that Pd@DHImel, with the highest product yields and lowest Pd loading, is the most efficient catalyst, even when working with deactivated aromatic iodides. Finally, stability tests indicated that the hybrid did not suffer leaching phenomena, leading to high yields for up to eight cycles.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Catalytic Cross-Coupling Reactions · melanin and skin pigmentation · Nanomaterials for catalytic reactions

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

Affiliations

Department of Chemical Sciences, University of Naples Federico II, via Cintia 4, I-80126 Naples, Italy

Bioelectronics Task Force, University of Naples Federico II, via Cintia 4, I-80126 Naples, Italy

Dipartimento di Scienze e Tecnologie Biologiche e Ambientali (Di.S.Te.B.A.), Università del Salento, via Monteroni 165, I-73100 Lecce, Italy

Dipartimento di Chimica and CSGI − Bari Unit, Università degli Studi di Bari Aldo Moro, Via Orabona 4, I-70126 Bari, Italy

Department of Chemistry, University of Warwick, Library Road, CV4 7AL Coventry, United Kingdom

School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Ave, Singapore 639798, Singapore

Institute of Crystallography (CNR-IC), National Council of Research, Via G. Amendola 122/O, I-70126 Bari, Italy

Funding

Leverhulme Trust · Ministero dell'Universit? e della Ricerca · Nanyang Technological University

References (44)

Show source-provided references
1. 10.1016/j.cherd.2024.07.01410.1016/j.cherd.2024.07.014 ↗
2. 10.1002/chem.20230355210.1002/chem.202303552 ↗
3. 10.1021/acs.chemrev.2c0087910.1021/acs.chemrev.2c00879 ↗
4. 10.1002/anie.20170840810.1002/anie.201708408 ↗
5. 10.1002/anie.20230930510.1002/anie.202309305 ↗
6. 10.1002/smll.20250474610.1002/smll.202504746 ↗
7. 10.1039/D3EY00265A10.1039/D3EY00265A ↗
8. 10.1016/j.ccr.2023.21552410.1016/j.ccr.2023.215524 ↗
9. 10.1111/pcmr.1239310.1111/pcmr.12393 ↗
10. 10.1021/acsomega.2c0064110.1021/acsomega.2c00641 ↗
11. 10.1111/pcmr.1212110.1111/pcmr.12121 ↗
12. 10.1038/s43246-024-00602-410.1038/s43246-024-00602-4 ↗
13. 10.3390/ijms2601041610.3390/ijms26010416 ↗
14. 10.1002/chem.20170195110.1002/chem.201701951 ↗
15. 10.1039/D0TB00623H10.1039/D0TB00623H ↗
16. 10.1002/anie.20191427610.1002/anie.201914276 ↗
17. 10.1021/acsami.3c0333710.1021/acsami.3c03337 ↗
18. 10.1002/ejoc.20240019110.1002/ejoc.202400191 ↗
19. 10.1039/C8MH00715B10.1039/C8MH00715B ↗
20. 10.1016/j.jcat.2018.02.03110.1016/j.jcat.2018.02.031 ↗
21. 10.1016/j.tetlet.2017.04.06210.1016/j.tetlet.2017.04.062 ↗
22. 10.1007/s11164-021-04651-z10.1007/s11164-021-04651-z ↗
23. 10.1021/acscatal.4c0234810.1021/acscatal.4c02348 ↗
24. 10.1016/j.cej.2024.15804510.1016/j.cej.2024.158045 ↗
25. 10.1021/acssuschemeng.1c0363410.1021/acssuschemeng.1c03634 ↗
26. 10.3390/catal1301021010.3390/catal13010210 ↗
27. 10.1016/j.jclepro.2021.12616410.1016/j.jclepro.2021.126164 ↗
28. 10.1002/ejoc.20240063210.1002/ejoc.202400632 ↗
29. 10.1021/jo901259s10.1021/jo901259s ↗
30. 10.1002/anie.20191427610.1002/anie.201914276 ↗
31. 10.1038/s42004-025-01731-810.1038/s42004-025-01731-8 ↗
32. 10.1039/C4TC01997K10.1039/C4TC01997K ↗
33. 10.1038/s41598-020-68773-x10.1038/s41598-020-68773-x ↗
34. 10.1149/1.298043410.1149/1.2980434 ↗
35. 10.1016/S0039-6028(02)01372-910.1016/S0039-6028(02)01372-9 ↗
36. 10.1002/ejoc.20220049710.1002/ejoc.202200497 ↗
37. 10.1021/acs.molpharmaceut.9b0015710.1021/acs.molpharmaceut.9b00157 ↗
38. 10.1016/j.mtsust.2022.10028310.1016/j.mtsust.2022.100283 ↗
39. 10.1007/s10570-012-9852-810.1007/s10570-012-9852-8 ↗
40. 10.1134/S002315842003021010.1134/S0023158420030210 ↗
41. 10.1016/j.molcata.2006.02.02410.1016/j.molcata.2006.02.024 ↗
42. 10.1016/j.tet.2016.03.08510.1016/j.tet.2016.03.085 ↗
43. 10.1039/C5RA01902H10.1039/C5RA01902H ↗
44. 10.1016/j.catcom.2013.03.01310.1016/j.catcom.2013.03.013 ↗