Rare nuclearities in Mn/oxo cluster chemistry: Synthesis and characterization of a mixed-valence {MnII/III11} complex bearing acetate and salicylhydroximate(-3) bridging/chelating ligands. (15th September 2021)
- Record Type:
- Journal Article
- Title:
- Rare nuclearities in Mn/oxo cluster chemistry: Synthesis and characterization of a mixed-valence {MnII/III11} complex bearing acetate and salicylhydroximate(-3) bridging/chelating ligands. (15th September 2021)
- Main Title:
- Rare nuclearities in Mn/oxo cluster chemistry: Synthesis and characterization of a mixed-valence {MnII/III11} complex bearing acetate and salicylhydroximate(-3) bridging/chelating ligands
- Authors:
- Koumousi, Evangelia S.
Lazari, Gerasimi
Grammatikopoulos, Spyridon
Papatriantafyllopoulou, Constantina
Manos, Manolis J.
Perlepes, Spyros P.
Tasiopoulos, Anastasios J.
Christou, George
Stamatatos, Theocharis C. - Abstract:
- Graphical abstract: The 2:1:2 reaction between Mn(O2 CMe)2 ·4H2 O, salicylhydroxamic acid (shaH2 ) and Me4 NOH·5H2 O has afforded the mixed-valent compound (Me4 N)4 [Mn II 2 Mn III 9 O4 (O2 CMe)9 (shi)6 ] (1 ), which consists of four vertex-sharing {Mn III 3 (μ3 -O 2− )} 7+ triangular subunits linked to each other and the Mn II atoms through the oximato arms of six shi 3− and the carboxylate O-atoms of nine supporting MeCO2 − groups. Abstract: The one-pot reaction between Mn(O2 CMe)2 ·4H2 O, salicylhydroxamic acid (shaH2 ) and Me4 NOH·5H2 O in a molar ratio of 2:1:2, and a solvent mixture comprising MeCN and MeOH, affords the new mixed-valence cluster compound (Me4 N)4 [Mn II 2 Mn III 9 O4 (O2 CMe)9 (shi)6 ] (1 ) in moderate yields. The anion of the tetradentate (N, O, O, O) chelating/bridging ligand shi 3− resulted from the in-situ metal ion-assisted amide-iminol tautomerism of shaH2 . The [Mn II 2 Mn III 9 (μ3 -O)4 (μ-OR)3 (μ3 -NO)6 ] 14+ core of 1 comprises four vertex-sharing {Mn III 3 (μ3 -O 2− )} 7+ triangular subunits of different types, which are linked to each other and the Mn II atoms through the oximato arms and the carboxylate O-atoms of six η 1 :η 1 :η 1 :η 2 :μ3 shi 3− and three η 1 :η 2 :μ3 MeCO2 − groups, respectively. Peripheral ligation about the core is provided by six η 1 :η 1 :μ MeCO2 − groups and the chelating parts of the shi 3− ligands. Solid-state direct-current (dc) magnetic susceptibility studies revealed the presence of predominantGraphical abstract: The 2:1:2 reaction between Mn(O2 CMe)2 ·4H2 O, salicylhydroxamic acid (shaH2 ) and Me4 NOH·5H2 O has afforded the mixed-valent compound (Me4 N)4 [Mn II 2 Mn III 9 O4 (O2 CMe)9 (shi)6 ] (1 ), which consists of four vertex-sharing {Mn III 3 (μ3 -O 2− )} 7+ triangular subunits linked to each other and the Mn II atoms through the oximato arms of six shi 3− and the carboxylate O-atoms of nine supporting MeCO2 − groups. Abstract: The one-pot reaction between Mn(O2 CMe)2 ·4H2 O, salicylhydroxamic acid (shaH2 ) and Me4 NOH·5H2 O in a molar ratio of 2:1:2, and a solvent mixture comprising MeCN and MeOH, affords the new mixed-valence cluster compound (Me4 N)4 [Mn II 2 Mn III 9 O4 (O2 CMe)9 (shi)6 ] (1 ) in moderate yields. The anion of the tetradentate (N, O, O, O) chelating/bridging ligand shi 3− resulted from the in-situ metal ion-assisted amide-iminol tautomerism of shaH2 . The [Mn II 2 Mn III 9 (μ3 -O)4 (μ-OR)3 (μ3 -NO)6 ] 14+ core of 1 comprises four vertex-sharing {Mn III 3 (μ3 -O 2− )} 7+ triangular subunits of different types, which are linked to each other and the Mn II atoms through the oximato arms and the carboxylate O-atoms of six η 1 :η 1 :η 1 :η 2 :μ3 shi 3− and three η 1 :η 2 :μ3 MeCO2 − groups, respectively. Peripheral ligation about the core is provided by six η 1 :η 1 :μ MeCO2 − groups and the chelating parts of the shi 3− ligands. Solid-state direct-current (dc) magnetic susceptibility studies revealed the presence of predominant antiferromagnetic exchange interactions between the Mn centers, mainly promoted by the coplanarity of the μ3 -O 2− within the {Mn3 } triangular planes and the insignificant distortion of the MnNOMn bridging units. Low-lying excited states precluded obtaining a good fit from the magnetization data, and the ground state was instead determined from the alternating-current (ac) data, which indicated an S = 3 ground state for 1 . The combined results emphasize the continuing supply from the use of the salicylhydroxime chelating/bridging ligand of new 3d-metal clusters of very rare nuclearities and beautiful molecular structures. … (more)
- Is Part Of:
- Polyhedron. Volume 206(2021)
- Journal:
- Polyhedron
- Issue:
- Volume 206(2021)
- Issue Display:
- Volume 206, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 206
- Issue:
- 2021
- Issue Sort Value:
- 2021-0206-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-09-15
- Subjects:
- Coordination clusters -- Manganese -- Salicylhydroxamic acid -- Undecanuclearity -- Magnetochemistry
Chemistry, Inorganic -- Periodicals
Chimie inorganique -- Périodiques
Organometaalverbindingen
Anorganische chemie
546.05 - Journal URLs:
- http://www.sciencedirect.com/science/journal/02775387 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.poly.2021.115298 ↗
- Languages:
- English
- ISSNs:
- 0277-5387
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.690000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18384.xml