Chiral Diuranyl(VI) Complexes and Their Catecholase Activities: Experimental and Theoretical Insights. Issue 14 (7th April 2022)
- Record Type:
- Journal Article
- Title:
- Chiral Diuranyl(VI) Complexes and Their Catecholase Activities: Experimental and Theoretical Insights. Issue 14 (7th April 2022)
- Main Title:
- Chiral Diuranyl(VI) Complexes and Their Catecholase Activities: Experimental and Theoretical Insights
- Authors:
- Ghosh, Sabari
Srivastava, Ankit K.
Sharma, Manju
Pal, Samudranil - Abstract:
- Abstract: Two enantiomeric pairs of complexes, [(UO2 )2 ( R/S ‐L 1 )2 (H2 O)2 ] ⋅ 2MeCN and [(UO2 )2 ( R/S ‐L 2 )2 (Me2 NCHO)2 ] (H2 R/S ‐L 1 = R/S ‐ N ‐(salicylidene)‐2‐amino‐1‐propanol and H2 R/S ‐L 2 = R/S ‐ N ‐(2‐hydroxy‐1‐naphthylidene)‐2‐amino‐1‐propanol) and their characterization by elemental analysis, mass spectrometry, various spectroscopy and X‐ray crystallography are reported. In each complex, trans ‐UO2 2+ units are in edge‐shared NO4 pentagonal planes formed by the two alkoxide end bridging ONO‐donor ( R/S ‐L 1/2 ) 2− and the two solvent molecules. The first pair is inactive, while the second pair is active towards catecholase activity. The mass spectra suggest formation of the adduct {complex−Me2 NCHO+substrate} and EPR spectra indicate a radical pathway for the catalytic reaction. Computational studies indicate that primarily the binding strength of the solvent molecule dictates the adduct formation and hence the catalytic inactivity/activity. Based on experimental observations and theoretical calculations a four step mechanism has been proposed for the catalytic activities of the second pair of complexes. Abstract : The enantiomeric pairs of complexes [(UO2 )2 ( R/S ‐L 1 )2 (H2 O)2 ] and [(UO2 )2 ( R/S ‐L 2 )2 (Me2 NCHO)2 ] (H2 R/S ‐L 1 = R/S ‐ N ‐(salicylidene)‐2‐amino‐1‐propanol and H2 R/S ‐L 2 = R/S ‐ N ‐(2‐hydroxy‐1‐naphthylidene)‐2‐amino‐1‐propanol) are reported. Catecholase inactivity of the first pair and activity of the second pair are demonstratedAbstract: Two enantiomeric pairs of complexes, [(UO2 )2 ( R/S ‐L 1 )2 (H2 O)2 ] ⋅ 2MeCN and [(UO2 )2 ( R/S ‐L 2 )2 (Me2 NCHO)2 ] (H2 R/S ‐L 1 = R/S ‐ N ‐(salicylidene)‐2‐amino‐1‐propanol and H2 R/S ‐L 2 = R/S ‐ N ‐(2‐hydroxy‐1‐naphthylidene)‐2‐amino‐1‐propanol) and their characterization by elemental analysis, mass spectrometry, various spectroscopy and X‐ray crystallography are reported. In each complex, trans ‐UO2 2+ units are in edge‐shared NO4 pentagonal planes formed by the two alkoxide end bridging ONO‐donor ( R/S ‐L 1/2 ) 2− and the two solvent molecules. The first pair is inactive, while the second pair is active towards catecholase activity. The mass spectra suggest formation of the adduct {complex−Me2 NCHO+substrate} and EPR spectra indicate a radical pathway for the catalytic reaction. Computational studies indicate that primarily the binding strength of the solvent molecule dictates the adduct formation and hence the catalytic inactivity/activity. Based on experimental observations and theoretical calculations a four step mechanism has been proposed for the catalytic activities of the second pair of complexes. Abstract : The enantiomeric pairs of complexes [(UO2 )2 ( R/S ‐L 1 )2 (H2 O)2 ] and [(UO2 )2 ( R/S ‐L 2 )2 (Me2 NCHO)2 ] (H2 R/S ‐L 1 = R/S ‐ N ‐(salicylidene)‐2‐amino‐1‐propanol and H2 R/S ‐L 2 = R/S ‐ N ‐(2‐hydroxy‐1‐naphthylidene)‐2‐amino‐1‐propanol) are reported. Catecholase inactivity of the first pair and activity of the second pair are demonstrated and probed. … (more)
- Is Part Of:
- ChemistrySelect. Volume 7:Issue 14(2022)
- Journal:
- ChemistrySelect
- Issue:
- Volume 7:Issue 14(2022)
- Issue Display:
- Volume 7, Issue 14 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 14
- Issue Sort Value:
- 2022-0007-0014-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-04-07
- Subjects:
- Catecholase activity -- Chiral ligands -- Diuranyl(VI) complexes -- Mechanism -- Structures
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202200293 ↗
- 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:
- 26778.xml