Synthesis, Characterization, and Catalytic Reactivities of Novel Dinuclear Cu(II) Complexes : Efficient Ring Opening Reaction of Epoxide. Issue 16 (24th April 2023)
- Record Type:
- Journal Article
- Title:
- Synthesis, Characterization, and Catalytic Reactivities of Novel Dinuclear Cu(II) Complexes : Efficient Ring Opening Reaction of Epoxide. Issue 16 (24th April 2023)
- Main Title:
- Synthesis, Characterization, and Catalytic Reactivities of Novel Dinuclear Cu(II) Complexes : Efficient Ring Opening Reaction of Epoxide
- Authors:
- Ahn, Hye Mi
Lee, Jiyoung
Lee, Minji
Kim, Yong Sung
Yun, Jin Yeong
Lee, Jae Jun
Kim, Sung‐Jin
Kim, Youngmee
Kim, Cheal - Abstract:
- Abstract: Novel tridentate N2 O‐type ligands L1 –L4 (((((X‐benzyl)pyridine‐2‐yl)methylamino)methyl)phenol); L1 for X=4‐CH3, L2 for X=H, L3 for X=2‐F, L4 for X=4‐CF3 ) and their dinuclear copper(II) complexes C1 –C4 (C1 for [(L1 )2 Cu2 (NO3 )2 ], C2 for [(L2 )2 Cu2 (NO3 )2 ], C3 for [(L3 )2 Cu2 (NO3 )2 ] and C4 for [(L4 )2 Cu2 (NO3 )2 ]) was synthesized and verified by 1 H NMR, IR, and ESI‐Mass. The structural forms of the copper complexes were determined by X‐ray crystallography. The dinuclear copper complexes C1 –C4 showed efficient ring‐opening properties of epoxides with methanol under mild conditions. In particular, the copper complex C1 having electron‐donating group in the ligand showed the most efficient reactivity in the ring opening of epoxides. The sole attack at the benzylic carbon of styrene oxide and the less steric preference in 1, 2‐epoxyhexane demonstrated that the regiochemistry of the ring opening catalyzed by dinuclear copper complexes might be dependent on the electronic feature of epoxide. Abstract : Novel tridentate N2 O‐type ligands L1–L4 and their dinuclear copper(II) complexes C1–C4 (C1 for [(L1)2 Cu2 (NO3 )2 ], C2 for [(L2)2 Cu2 (NO3 )2 ], C3 for [(L3)2 Cu2 (NO3 )2 ] and C4 for [(L4)2 Cu2 (NO3 )2 ]) was synthesized and characterized. The dinuclear copper complexes C1‐C4 showed efficient ring‐opening properties of epoxides with methanol under mild conditions. In particular, the copper complex C1 having electron‐donating group in the ligand showed theAbstract: Novel tridentate N2 O‐type ligands L1 –L4 (((((X‐benzyl)pyridine‐2‐yl)methylamino)methyl)phenol); L1 for X=4‐CH3, L2 for X=H, L3 for X=2‐F, L4 for X=4‐CF3 ) and their dinuclear copper(II) complexes C1 –C4 (C1 for [(L1 )2 Cu2 (NO3 )2 ], C2 for [(L2 )2 Cu2 (NO3 )2 ], C3 for [(L3 )2 Cu2 (NO3 )2 ] and C4 for [(L4 )2 Cu2 (NO3 )2 ]) was synthesized and verified by 1 H NMR, IR, and ESI‐Mass. The structural forms of the copper complexes were determined by X‐ray crystallography. The dinuclear copper complexes C1 –C4 showed efficient ring‐opening properties of epoxides with methanol under mild conditions. In particular, the copper complex C1 having electron‐donating group in the ligand showed the most efficient reactivity in the ring opening of epoxides. The sole attack at the benzylic carbon of styrene oxide and the less steric preference in 1, 2‐epoxyhexane demonstrated that the regiochemistry of the ring opening catalyzed by dinuclear copper complexes might be dependent on the electronic feature of epoxide. Abstract : Novel tridentate N2 O‐type ligands L1–L4 and their dinuclear copper(II) complexes C1–C4 (C1 for [(L1)2 Cu2 (NO3 )2 ], C2 for [(L2)2 Cu2 (NO3 )2 ], C3 for [(L3)2 Cu2 (NO3 )2 ] and C4 for [(L4)2 Cu2 (NO3 )2 ]) was synthesized and characterized. The dinuclear copper complexes C1‐C4 showed efficient ring‐opening properties of epoxides with methanol under mild conditions. In particular, the copper complex C1 having electron‐donating group in the ligand showed the most efficient reactivity in the ring opening of epoxides. … (more)
- Is Part Of:
- ChemistrySelect. Volume 8:Issue 16(2023)
- Journal:
- ChemistrySelect
- Issue:
- Volume 8:Issue 16(2023)
- Issue Display:
- Volume 8, Issue 16 (2023)
- Year:
- 2023
- Volume:
- 8
- Issue:
- 16
- Issue Sort Value:
- 2023-0008-0016-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2023-04-24
- Subjects:
- dinuclear copper complexes -- epoxide -- methanolysis -- ring-opening reaction
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202300218 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 27019.xml