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DOI: 10.1055/a-2732-6914
Palladium Supported on Calcined Coconut Shell Fiber (Pd/CCSF) as an Efficient and Sustainable Catalyst: Microwave-Assisted Synthesis of C–S Cross-Coupling Derivatives in DMF
Authors

Abstract
The palladium supported on calcined coconut shell fiber (Pd/CCSF) catalyst was synthesized using an eco-friendly agro-industrial material, CCSF, with PdCl₂ supported on it. This catalyst was used for the first time in the development of a C–S cross-coupling reaction between various benzene thiols and 4,7-dibromo-2,1,3-benzothiadiazole or 5-bromo-2,1,3-benzothiadiazole under microwave irradiation at 75 °C (200 W, 100 psi) in DMF, with K₂CO₃ as the base. The catalyst was characterized using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) analyses. Furthermore, it was recycled and reused for up to four catalytic cycles without any loss of efficiency. A proposed mechanistic pathway for the C–S cross-coupling reaction is also included in this article.
Data Availability Statement
Data are available in the supplementary material of this article.
Publication History
Received: 02 June 2025
Accepted: 27 August 2025
Article published online:
10 November 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
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References
- 1 Gangjee A, Zeng Y, Talreja T, McGuire JJ, Kisliuk RL, Queener SF. J Med Chem 2007; 50: 3046
- 2 De Martino G, Edler MC, La Regina G. et al. J Med Chem 2006; 49: 947
- 3 Kondo T, Mitsudo T. Chem Rev 2000; 100: 3205
- 4 Ley SV, Thomas AW. Angew Chem Int Ed 2003; 42: 5400
- 5 Katla R, Katla R, Goulart TB, Rosa DS, Rosa GR. Synlett 2022; 33: 1637
- 6 Zhou WP, Cao ZC, Jiang SH. et al. Org Electron 2012; 13: 560
- 7 Li YL, Scudiero L, Ren TH, Dong WJ. J Photochem Photobiol A 2012; 231: 51
- 8 Xia D, Guo X, Chen L, Baumgarten M, Keerthi A, Müllen K. Angew Chem Int Ed 2016; 55: 941
- 9 Jung JW, Jo JW, Jung EH, Jo WH. Org Electron 2016; 31: 149
- 10 Cameron J, Abed MM, Chapman SJ. et al. J Mater Chem C 2018; 6: 3709
- 11 Mataka S, Takahashi K, Imura T, Tashiro M. J Heterocycl Chem 1982; 19: 1481
- 12 Gozzo F. J Agric Food Chem 2003; 51: 4487
- 13 Balasankar T, Gopalakrishnan M, Nagarajan S. Eur J Med Chem 2005; 40: 728
- 14 dos Santos BF, Pereira CF, Pinz MP. et al. Appl Organomet Chem 2020; e5650
- 15 Balaguez RA, Ricordi VG, Duarte RC. et al. RSC Adv 2016; 6: 49613
- 16 Kukreja G, Phukan S, Kodam J. et al. WO2013005157 A1 2013
- 17 Katla R, Katla R, Oreste EQ, Kessler F. Synthesis 2023; 55: 799-807
- 18 Katla R, Katla R, Domingues NLC. Synthesis 2023; 55: 826
- 19 Katla R, Katla R, Domingues NLC. Synthesis 2022; 54: 4608
- 20 Katla R, Katla R. New J Chem 2022; 46: 13918
- 21 Schmitt CR, Rosa DS, Vargas BP. et al. J Clean Prod 2018; 185: 342