Luminescent Tetrahedral Manganese(II) Pentaphluorophenolate Complex as a Highly Sensitive Molecular Thermometer

Abstract

A mononuclear tetrahedral manganese complex containing all O-donor ligands has been prepared under mild conditions starting from a dialkylcarbamato manganese(II) precursor. Manganese(II) N,N-dibutylcarbamate [Mn(O₂CNBu₂)₂]_n, 1, can be conveniently prepared by extraction from a deoxygenated water solution of manganese(II) sulfate using a CO₂-saturated toluene solution of dibutylamine. Access to the N,N-dibenzylcarbamato manganese complex [Mn(O₂CNBz₂)₂]_n, 2, occurs through metathesis by reaction with dibenzylamine and carbon dioxide. By reaction of 2 with pentafluorophenol, an almost quantitative reaction affords [Bz₂NH₂]₂[Mn(OC₆F₅)₄], 3, that has been crystallographically characterized through single-crystal X-ray diffraction. Compound 3 exhibits absorption and emission spectral features characteristic of Mn²⁺ ions in a tetrahedral coordination environment. Upon cooling, the emission intensity was observed to increase by approximately two orders of magnitude. The excited-state lifetimes exhibited significant temperature dependence, ranging from 12.7 ms at 80 K to 10 μs at 290 K. The temperature-dependent trends of both emission intensity and lifetimes showed nearly identical profiles. As a result, compound 3 functions as a dual-mode highly sensitive luminescent molecular thermometer, with a maximum relative thermal sensitivity (S_r) of 7.4% K^–1 at 220 K and S_r >1 over the temperature range 170–270 K. A distinctive feature of compound 3 is its capacity to yield equivalent luminescent molecular thermometers (LMT) using either the emission intensity or lifetime, thus enhancing its versatility in thermal sensing applications.