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Fluorinated Mn(III)/(II)-Porphyrin with Redox-Responsive 1 H and 19 F Relaxation Properties.
Pinto, Sara M A; Ferreira, Ana R R; Teixeira, Daniela S S; Nunes, Sandra C C; Batista de Carvalho, Ana L M; Almeida, Joseany M S; Garda, Zoltan; Pallier, Agnés; Pais, Alberto A C C; Brett, Christopher M A; Tóth, Éva; Marques, Maria P M; Pereira, Mariette M; Geraldes, Carlos F G C.
  • Pinto SMA; University of Coimbra, CQC-IMS, Department of Chemistry, P-3004-535, Coimbra, Portugal.
  • Ferreira ARR; Coimbra Chemistry Center, University of Coimbra, Rua Larga Largo D. Dinis, 3004-535, Coimbra, Portugal.
  • Teixeira DSS; University of Coimbra, CQC-IMS, Department of Chemistry, P-3004-535, Coimbra, Portugal.
  • Nunes SCC; Coimbra Chemistry Center, University of Coimbra, Rua Larga Largo D. Dinis, 3004-535, Coimbra, Portugal.
  • Batista de Carvalho ALM; University of Coimbra, CQC-IMS, Department of Chemistry, P-3004-535, Coimbra, Portugal.
  • Almeida JMS; Coimbra Chemistry Center, University of Coimbra, Rua Larga Largo D. Dinis, 3004-535, Coimbra, Portugal.
  • Garda Z; University of Coimbra, CQC-IMS, Department of Chemistry, P-3004-535, Coimbra, Portugal.
  • Pallier A; Coimbra Chemistry Center, University of Coimbra, Rua Larga Largo D. Dinis, 3004-535, Coimbra, Portugal.
  • Pais AACC; Molecular Physical Chemistry R&D Unit Department of Chemistry, University of Coimbra, Rua Larga, 3004-535, Coimbra, Portugal.
  • Brett CMA; Department of Life Sciences, Faculty of Science and Technology, Calçada Martim de Freitas, 3000-393, Coimbra, Portugal.
  • Tóth É; University of Coimbra, CQC-IMS, Department of Chemistry, P-3004-535, Coimbra, Portugal.
  • Marques MPM; CEMMPRE, University of Coimbra, Pinhal de Marrocos, 3030-788, Coimbra, Portugal.
  • Pereira MM; Centre de Biophysique Moléculaire, CNRS, UPR 4301, Université d'Orléans, Rue Charles Sadron, 45071, Orléans Cedex 2, France.
  • Geraldes CFGC; Centre de Biophysique Moléculaire, CNRS, UPR 4301, Université d'Orléans, Rue Charles Sadron, 45071, Orléans Cedex 2, France.
Chemistry ; 29(53): e202301442, 2023 Sep 21.
Article en En | MEDLINE | ID: mdl-37606898
ABSTRACT
A new fluorinated manganese porphyrin, (Mn-TPP-p-CF3 ) is reported capable of providing, based on the Mn(III)/Mn(II) equilibrium, dual 1 H relaxivity and 19 F NMR response to redox changes. The physical-chemical characterization of both redox states in DMSO-d6 /H2 O evidenced that the 1 H relaxometric and 19 F NMR properties are appropriate for differential redox MRI detection. The Mn(III)-F distance (dMn-F =9.7-10 Å), as assessed by DFT calculations, is well tailored to allow for adequate paramagnetic effect of Mn(III) on 19 F T1 and T2 relaxation times. Mn-TPP-p-CF3 has a reversible Mn(II)/Mn(III) redox potential of 0.574 V vs. NHE in deoxygenated aqueous HEPES/ THF solution. The reduction of Mn(III)-TPP-p-CF3 in the presence of ascorbic acid is slowly, but fully reversed in the presence of air oxygen, as monitored by UV-Vis spectrometry and 19 F NMR. The broad 1 H and 19 F NMR signals of Mn(III)-TPP-p-CF3 disappear in the presence of 1 equivalent ascorbate replaced by a shifted and broadened 19 F NMR signal from Mn(II)-TPP-p-CF3 . Phantom 19 F MR images in DMSO show a MRI signal intensity decrease upon reduction of Mn(III)-TPP-p-CF3 , retrieved upon complete reoxidation in air within ~24 h. 1 H NMRD curves of the Mn(III)/(II)-TPP-p-CF3 chelates in mixed DMSO/water solvent have the typical shape of Mn(II)/Mn(III) porphyrins.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article