repository
CO2/Propylene Oxide Copolymerization with a Bifunctional Catalytic System Composed of Multiple Ammonium Salts and a Salen Cobalt Complex Containing Sulfonate Anions
- Author(s)
- 현용빈
- Advisor
- 이분열
- Department
- 일반대학원 분자과학기술학과
- Publisher
- The Graduate School, Ajou University
- Publication Year
- 2022-02
- Language
- eng
- Keyword
- CO2; Copolymerization; Multiple ammonium salts; Salen
- Alternative Abstract
- A (Salen)Co(III) complex tethering four quaternary ammonium salts with covalent bonds is one of the most highly active catalysts for CO2/epoxide copolymerization. In this work, we aimed to prepare similar (Salen)Co(III) complexes to which quaternary ammonium salts are linked via ionic interactions. Thus, multiple ammonium salts containing 2-5 quaternary ammonium salt units and (Salen)Co(III) complexes containing one or two SO3[PhNH3]+ moieties were prepared. A binary catalytic system composed of the prepared multiple ammonium salts and the prepared (Salen)Co(III) complex containing -SO3-[(nBu)4N]+ moieties showed high activity (TOF, 15004500 h1) for CO2/propylene oxide (PO) copolymerization, whereas a combination of the multiple ammonium salts and the conventional (Salen)Co(III) complex not containing -SO3-[(nBu)4N]+ moieties was inactive under the identical polymerization conditions of [PO]/[Co] = 20000. However, a substantial amount of cyclic carbonate was concomitantly generated, especially when a (Salen)Co(III) complex containing two -SO3-[(nBu)4N]+ moieties was used (2530%). This side-reaction could be mitigated by ca. 50% by employing a (Salen)Co(III) complex containing one -SO3-[(nBu)4N]+ moiety. Cyclic carbonate generation can reasonably be ascribed to ammonium salts ([(nBu)4N]+[carbonate]-) not linked to the (Salen)Co(III) complex formed in the binary catalytic system.
- Fulltext
- Appears in Collections:
- Graduate School of Ajou University > Department of Molecular Science and Technology > 3. Theses(Master)
- Files in This Item:
- There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
-
- License
- STATISTICS
- Total Visit :3,635,427
- Total Download :1,804
- Today View :2,607
