TY - JOUR
T1 - A pentadentate member of the picolinate family for Mn(ii) complexation and an amphiphilic derivative
AU - Pujales-Paradela, Rosa
AU - Carniato, Fabio
AU - Uzal-Varela, Rocío
AU - Brandariz, Isabel
AU - Iglesias, Emilia
AU - Platas-Iglesias, Carlos
AU - Botta, Mauro
AU - Esteban-Gómez, David
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - We report a pentadentate ligand containing a 2,2′-azanediyldiacetic acid moiety functionalized with a picolinate group at the nitrogen atom (H 3 paada), as well as a lipophylic derivative functionalized with a dodecyloxy group at position 4 of the pyridyl ring (H 3 C 12 Opaada). The protonation constants of the paada 3− ligand and the stability constant of the Mn(ii) complex were determined using a combination of potentiometric and spectrophotometric titrations (25 °C, 0.15 M NaCl). A detailed relaxometric characterisation was accomplished by recording 1 H Nuclear Magnetic Relaxation Dispersion (NMRD) profiles and 17 O chemical shifts and relaxation rates. These studies provide detailed information on the microscopic parameters that control their efficiency as relaxation agents in vitro. For the sake of completeness and to facilitate comparison, we also characterised the related [Mn(nta)] − complex (nta = nitrilotriacetate). Both the [Mn(paada)] − and [Mn(nta)] − complexes turned out to contain two inner-sphere water molecules in aqueous solution. The exchange rate of these coordinated water molecules was slower in [Mn(paada)] − (k298ex = 90 × 10 7 s −1 ) than in [Mn(nta)] − (k298ex = 280 × 10 7 s −1 ). The complexes were also characterised using both DFT (TPSSh/def2-TZVP) and ab initio CAS(5,5) calculations. The lipophylic [Mn(C 12 Opaada)] − complex forms micelles in solution characterised by a critical micellar concentration (cmc) of 0.31 ± 0.01 mM. This complex also forms a rather strong adduct with Bovine Serum Albumin (BSA) with an association constant of 5.5 × 10 4 M −1 at 25 °C. The enthalpy and entropy changes obtained for the formation of the adduct indicate that the binding event is driven by hydrophobic interactions.
AB - We report a pentadentate ligand containing a 2,2′-azanediyldiacetic acid moiety functionalized with a picolinate group at the nitrogen atom (H 3 paada), as well as a lipophylic derivative functionalized with a dodecyloxy group at position 4 of the pyridyl ring (H 3 C 12 Opaada). The protonation constants of the paada 3− ligand and the stability constant of the Mn(ii) complex were determined using a combination of potentiometric and spectrophotometric titrations (25 °C, 0.15 M NaCl). A detailed relaxometric characterisation was accomplished by recording 1 H Nuclear Magnetic Relaxation Dispersion (NMRD) profiles and 17 O chemical shifts and relaxation rates. These studies provide detailed information on the microscopic parameters that control their efficiency as relaxation agents in vitro. For the sake of completeness and to facilitate comparison, we also characterised the related [Mn(nta)] − complex (nta = nitrilotriacetate). Both the [Mn(paada)] − and [Mn(nta)] − complexes turned out to contain two inner-sphere water molecules in aqueous solution. The exchange rate of these coordinated water molecules was slower in [Mn(paada)] − (k298ex = 90 × 10 7 s −1 ) than in [Mn(nta)] − (k298ex = 280 × 10 7 s −1 ). The complexes were also characterised using both DFT (TPSSh/def2-TZVP) and ab initio CAS(5,5) calculations. The lipophylic [Mn(C 12 Opaada)] − complex forms micelles in solution characterised by a critical micellar concentration (cmc) of 0.31 ± 0.01 mM. This complex also forms a rather strong adduct with Bovine Serum Albumin (BSA) with an association constant of 5.5 × 10 4 M −1 at 25 °C. The enthalpy and entropy changes obtained for the formation of the adduct indicate that the binding event is driven by hydrophobic interactions.
UR - http://www.scopus.com/inward/record.url?scp=85059380374&partnerID=8YFLogxK
U2 - 10.1039/C8DT03856B
DO - 10.1039/C8DT03856B
M3 - Article
SN - 1477-9226
VL - 48
SP - 696
EP - 710
JO - Dalton Transactions
JF - Dalton Transactions
IS - 2
ER -