“…[13,14,27,28,34,35,[45][46][47][48] A second red-shifted transition ChemPlusChem with lower intensity is observed for the gold(I) compounds 1 c and 2 that could be ascribed to different conformers/dimers on the ground state where aurophilic interactions are involved [16] or to or a charge transfer transition in which a gold atom is involved. [5,49,50] The emission spectra of the compounds show the typical fluorescence band from the π-π* of the coumarin that is centred at ca. 450 nm, being 7 nm blue-shifted for the gold(I) complexes with respect to the emission of L [13,14,27,28,34,35,45] The emission quantum yields are in all cases between 20-25 % where there is not any relevant effect of the phosphane on the resulting emission efficiency but it is the double for gold(I) complexes in comparison with L, as previously observed in other gold(I)-coumarin derivatives.…”