<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Golovenko EA</submitter><funding>Ministry of Science and Higher Education of the Russian Federation</funding><pagination>3066</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12656307</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(22)</volume><pubmed_abstract>A carbon-supported palladium-containing polysiloxane macrocatalyst (Pd-PDMS) was developed for pharmaceutical-grade cross-coupling reactions. The catalyst demonstrates exceptional year-long stability at room temperature while maintaining full catalytic activity. Pd-PDMS efficiently promotes three pharmaceutically relevant reactions: Suzuki coupling (80% yield), copper-free Sonogashira coupling (90% yield at 55 °C), and Heck coupling (80% yield at 90 °C). The copper-free Sonogashira protocol eliminates toxic copper cocatalysts, phosphine ligands, and organic bases while operating under mild conditions. Most significantly, palladium contamination in products reaches ultra-low levels of 22 ppb (Sonogashira, Suzuki) and 167 ppb (Heck), representing a 60-450-fold improvement over European Medicines Agency requirements (10 ppm). The catalyst exhibits excellent recyclability without activity loss over multiple cycles, with simple washing protocols between uses. Scanning electron microscopy and X-ray photoelectron spectroscopy confirmed uniform Pd-PDMS coating on carbon fibers, while density functional theory calculations revealed specific coordination interactions between the palladium complex and carbon support at 3.26 Å distance. This convergence of pharmaceutical-grade metal contamination control, exceptional stability, and multi-reaction versatility establishes a significant advancement for sustainable cross-coupling catalysis in pharmaceutical applications.</pubmed_abstract><journal>Polymers</journal><pubmed_title>Recyclable Palladium-Polysiloxane Catalyst with Ultra-Low Metal Leaching for Drug Synthesis.</pubmed_title><pmcid>PMC12656307</pmcid><funding_grant_id>075-15-2024-553</funding_grant_id><pubmed_authors>Golovenko EA</pubmed_authors><pubmed_authors>Kukushkin VY</pubmed_authors><pubmed_authors>Boyarskiy VP</pubmed_authors><pubmed_authors>Baykov SV</pubmed_authors><pubmed_authors>Pankin DV</pubmed_authors><pubmed_authors>Islamova RM</pubmed_authors><pubmed_authors>Petrova PP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recyclable Palladium-Polysiloxane Catalyst with Ultra-Low Metal Leaching for Drug Synthesis.</name><description>A carbon-supported palladium-containing polysiloxane macrocatalyst (Pd-PDMS) was developed for pharmaceutical-grade cross-coupling reactions. The catalyst demonstrates exceptional year-long stability at room temperature while maintaining full catalytic activity. Pd-PDMS efficiently promotes three pharmaceutically relevant reactions: Suzuki coupling (80% yield), copper-free Sonogashira coupling (90% yield at 55 °C), and Heck coupling (80% yield at 90 °C). The copper-free Sonogashira protocol eliminates toxic copper cocatalysts, phosphine ligands, and organic bases while operating under mild conditions. Most significantly, palladium contamination in products reaches ultra-low levels of 22 ppb (Sonogashira, Suzuki) and 167 ppb (Heck), representing a 60-450-fold improvement over European Medicines Agency requirements (10 ppm). The catalyst exhibits excellent recyclability without activity loss over multiple cycles, with simple washing protocols between uses. Scanning electron microscopy and X-ray photoelectron spectroscopy confirmed uniform Pd-PDMS coating on carbon fibers, while density functional theory calculations revealed specific coordination interactions between the palladium complex and carbon support at 3.26 Å distance. This convergence of pharmaceutical-grade metal contamination control, exceptional stability, and multi-reaction versatility establishes a significant advancement for sustainable cross-coupling catalysis in pharmaceutical applications.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-05-19T03:19:12.59Z</modification><creation>2026-05-19T03:11:46.356Z</creation></dates><accession>S-EPMC12656307</accession><cross_references><pubmed>41304431</pubmed><doi>10.3390/polym17223066</doi></cross_references></HashMap>