An isocyanide ligand for the rapid quenching and efficient removal of copper residues after Cu/TEMPO-catalyzed aerobic alcohol oxidation and atom transfer radical polymerization. Issue 16 (15th April 2020)
- Record Type:
- Journal Article
- Title:
- An isocyanide ligand for the rapid quenching and efficient removal of copper residues after Cu/TEMPO-catalyzed aerobic alcohol oxidation and atom transfer radical polymerization. Issue 16 (15th April 2020)
- Main Title:
- An isocyanide ligand for the rapid quenching and efficient removal of copper residues after Cu/TEMPO-catalyzed aerobic alcohol oxidation and atom transfer radical polymerization
- Authors:
- Szczepaniak, Grzegorz
Piątkowski, Jakub
Nogaś, Wojciech
Lorandi, Francesca
Yerneni, Saigopalakrishna S.
Fantin, Marco
Ruszczyńska, Anna
Enciso, Alan E.
Bulska, Ewa
Grela, Karol
Matyjaszewski, Krzysztof - Abstract:
- Abstract : Three for the price of one: 1, 4-bis(3-isocyanopropyl)piperazine allows for the removal of Cu impurities, can quench Cu-catalyzed reactions, and can prevent undesirable Glaser coupling. Abstract : Transition metal catalysts play a prominent role in modern organic and polymer chemistry, enabling many transformations of academic and industrial significance. However, the use of organometallic catalysts often requires the removal of their residues from reaction products, which is particularly important in the pharmaceutical industry. Therefore, the development of efficient and economical methods for the removal of metal contamination is of critical importance. Herein, we demonstrate that commercially available 1, 4-bis(3-isocyanopropyl)piperazine can be used as a highly efficient quenching agent (QA ) and copper scavenger in Cu/TEMPO alcohol aerobic oxidation (Stahl oxidation) and atom transfer radical polymerization (ATRP). The addition of QA immediately terminates Cu-mediated reactions under various conditions, forming a copper complex that can be easily separated from both small molecules and macromolecules. The purification protocol for aldehydes is based on the addition of a small amount of silica gel followed by QA and filtration. The use of QA@SiO2 synthesized in situ results in products with Cu content usually below 5 ppm. Purification of polymers involves only the addition of QA in THF followed by filtration, leading to polymers with very low Cu content, evenAbstract : Three for the price of one: 1, 4-bis(3-isocyanopropyl)piperazine allows for the removal of Cu impurities, can quench Cu-catalyzed reactions, and can prevent undesirable Glaser coupling. Abstract : Transition metal catalysts play a prominent role in modern organic and polymer chemistry, enabling many transformations of academic and industrial significance. However, the use of organometallic catalysts often requires the removal of their residues from reaction products, which is particularly important in the pharmaceutical industry. Therefore, the development of efficient and economical methods for the removal of metal contamination is of critical importance. Herein, we demonstrate that commercially available 1, 4-bis(3-isocyanopropyl)piperazine can be used as a highly efficient quenching agent (QA ) and copper scavenger in Cu/TEMPO alcohol aerobic oxidation (Stahl oxidation) and atom transfer radical polymerization (ATRP). The addition of QA immediately terminates Cu-mediated reactions under various conditions, forming a copper complex that can be easily separated from both small molecules and macromolecules. The purification protocol for aldehydes is based on the addition of a small amount of silica gel followed by QA and filtration. The use of QA@SiO2 synthesized in situ results in products with Cu content usually below 5 ppm. Purification of polymers involves only the addition of QA in THF followed by filtration, leading to polymers with very low Cu content, even after ATRP with high catalyst loading. Furthermore, the addition of QA completely prevents oxidative alkyne–alkyne (Glaser) coupling. Although isocyanide QA shows moderate toxicity, it can be easily converted into a non-toxic compound by acid hydrolysis. … (more)
- Is Part Of:
- Chemical science. Volume 11:Issue 16(2020)
- Journal:
- Chemical science
- Issue:
- Volume 11:Issue 16(2020)
- Issue Display:
- Volume 11, Issue 16 (2020)
- Year:
- 2020
- Volume:
- 11
- Issue:
- 16
- Issue Sort Value:
- 2020-0011-0016-0000
- Page Start:
- 4251
- Page End:
- 4262
- Publication Date:
- 2020-04-15
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0sc00623h ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13954.xml