Ligand control of59co nuclear spin relaxation thermometry

Abstract

Studying the correlation between temperature-driven molecular structure and nuclear spin dynamics is essential to understanding fundamental design principles for thermometric nuclear magnetic resonance spin-based probes. Herein, we study the impact of progressively encapsulating ligands on temperature-dependent59Co T1 (spin–lattice) and T2 (spin–spin) relaxation times in a set of Co(III) complexes: K3[Co(CN)6] (1); [Co(NH3)6]Cl3 (2); [Co(en)3]Cl3 (3), en = ethylenediamine); [Co(tn)3]Cl3 (4), tn = trimethylenediamine); [Co(tame)2]Cl3 (5), tame = triaminomethylethane); and [Co(dinosar)]Cl3 (6), dinosar = dinitrosarcophagine). Measurements indicate that59Co T1 and T2 increase with temperature for 1–6 between 10 and 60◦C, with the greatest ∆T1/∆T and ∆T2/∆T temperature sensitivities found for 4 and 3, 5.3(3)%T1/◦C and 6(1)%T2/◦C, respectively. Temperature-dependent T2* (dephasing time) analyses were also made, revealing the highest ∆T2*/∆T sensitivities in structures of greatest encapsulation, as high as 4.64%T2*/◦C for 6. Calculations of the temperature-dependent quadrupolar coupling parameter, ∆e2qQ/ ∆T, enable insight into the origins of the relative ∆T1/∆T values. These results suggest tunable quadrupolar coupling interactions as novel design principles for enhancing temperature sensitivity in nuclear spin-based probes.