Roles of basicity and steric crowding of anionic coligands in catechol oxidase-like activity of Cu(ii)-Mn(ii) complexes.


Journal

Dalton transactions (Cambridge, England : 2003)
ISSN: 1477-9234
Titre abrégé: Dalton Trans
Pays: England
ID NLM: 101176026

Informations de publication

Date de publication:
18 Aug 2020
Historique:
pubmed: 8 8 2020
medline: 1 6 2021
entrez: 8 8 2020
Statut: ppublish

Résumé

Five new heterometallic Cu(ii)-Mn(ii) discrete trinuclear complexes, [(CuL)2Mn(CH3COO)2] (1), [(CuL)2Mn(NO3)2] (2), [(CuL)2Mn(C6H5COO)(H2O)]Cl (3), [(CuL)2Mn((p-OH)C6H5COO)(H2O)]ClO4 (4) and [(CuL)2Mn(HCOO)(H2O)]ClO4 (5), have been synthesized using a metalloligand, CuL derived from an N2O2 donor Schiff base, H2L (N,N'-bis(α-methylsalicylidene)-1,3-propanediamine). Single-crystal structural analyses reveal that all five complexes have a common [(CuL)2Mn] core, where two terminal metalloligands, CuL, are connected to the central metal ion, Mn(ii), via double phenoxido bridges. Among the complexes, 1 and 2 possess linear structures where the terminal Cu(ii) atoms are bridged to the central Mn(ii) atoms by acetate and nitrate ions, respectively along with the double phenoxido bridges, whereas 3, 4 and 5 have bent structures in which the respective anionic coligands, benzoate, p-hydroxybenzoate and formate ions are coordinated only to central Mn(ii) in monodentate fashion along with a water molecule that completes its hexa-coordinated geometry. Among the complexes, 1, 3, 4 and 5 show quite high bio-mimicking catecholase-like activity for the aerial oxidation of 3,5-di-tert-butylcatechol with turnover numbers (Kcat) of 139 h-1, 439 h-1, 348 h-1 and 730 h-1, respectively, whereas complex 2 is practically inactive towards this reaction. The presence of the coordinated water molecule to Mn(ii) in the bent complexes, 3-5, appears to be responsible for their high catalytic activity and the difference in their activity may be attributed to steric crowding due to the anionic coligand, whereas the inactivity of 2 seems to be associated with the low basicity of the nitrate ion. The temperature-dependent dc molar magnetic susceptibility measurements reveal that complexes 1-5 are antiferromagnetically coupled with the exchange coupling constants (J) = -8.54 cm-1, -11.50 cm-1, -19.83 cm-1, -10.65 cm-1 and -10.27 cm-1 for 1, 2, 3, 4 and 5 respectively as is expected from the Cu-O-Mn bridging angles.

Identifiants

pubmed: 32760992
doi: 10.1039/d0dt00952k
doi:

Substances chimiques

Anions 0
Benzoates 0
Coordination Complexes 0
Formates 0
Ligands 0
Parabens 0
Schiff Bases 0
Water 059QF0KO0R
formic acid 0YIW783RG1
Manganese 42Z2K6ZL8P
Copper 789U1901C5
4-hydroxybenzoic acid JG8Z55Y12H

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11268-11281

Auteurs

Sabarni Dutta (S)

Department of Chemistry, University College of Science, University of Calcutta, 92, A.P.C. Road, Kolkata 700 009, India. ghosh_59@yahoo.com.

Pradip Bhunia (P)

Department of Chemistry, University College of Science, University of Calcutta, 92, A.P.C. Road, Kolkata 700 009, India. ghosh_59@yahoo.com.

Júlia Mayans (J)

Departament de Química Inorgànica I Orgànica, Secció Inorgànica and Institut de Nanosciència I Nanotecnologia (IN2UB), Martíi Franqués 1-11, 08028, Barcelona, Spain.

Michael G B Drew (MGB)

School of Chemistry, The University of Reading, P.O. Box 224, Whiteknights, Reading RG6 6AD, UK.

Ashutosh Ghosh (A)

Department of Chemistry, University College of Science, University of Calcutta, 92, A.P.C. Road, Kolkata 700 009, India. ghosh_59@yahoo.com.

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Classifications MeSH