1H and 17O NMR Relaxometric and Computational Study on Macrocyclic Mn(II) Complexes

Herein we report a detailed H-1 and O-17 relaxometric investigation of Mn(II) complexes with cyclenbased ligands such as 2-(1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (DO IA), 2,2 '-(1,4,7,10-tetraazacyclododecane-1,4-diyI)diacetic acid (1,4-DO2A), 2,2 '-(1,4,7,10-tetraazacyclododecane1,7-diyOdiacetic acid (1,7-DO2A), and 2,2 ',2 ''-(1,4,7,10-tetraazacyclododecane-1,4,7-triyOtriacetic acid (DO3A). The Mn(II) complex with the heptadentate ligand DO3A does not have inner sphere water molecules (q = 0), and therefore, the metal ion is most likely seven-coordinate. The hexadentate DO2A ligand has two isomeric forms: 1,7-DO2A and 1,4-DO2A. The Mn(II) complex with 1,7-DO2A is predominantly six-coordinate (q= 0). In aqueous solutions of [Mn(1,4-DO2A)], a species with one coordinated water molecule (q = 1) prevails largely, whereas a q = 0 form represents only about 10% of the overall population. The Mn(II) complex of the pentadentate ligand DOIA also contains a coordinated water molecule. DFT calculations (B3LYP model) are used to obtain information about the structure of this family of closely related complexes in solution, as well as to determine theoretically the '70 and 1H hyperfine coupling constants responsible for the scalar contribution to O-17 and H-1 NMR relaxation rates and 170 NMR chemical shifts. These calculations provide O-17 A/h values of ca. 40 x 10(6) rad s(-1), in good agreement with experimental data. The [Mn(1,4-DO(2)A)(H2O)] complex is endowed with a relatively fast water exchange rate (Icex2 '' = 11.3 X 108 s-1) in comparison to the [Mn(EDTA)(H20)}2analogue (kr = 4.7 X 108 s-1), but about 5 times lower than that of the [Mn(D01A)(H20))* complex (1c,x2 ''= 60 X 108 s-1). The water exchange rate measured for the latter complex represents the highest water exchange rate ever measured for a Mn(II) complex.