摘要： Finding diverse and tunable molecular structures is relevant towards the design of functional nanostructures. The photoluminescence of complex 1, featuring ligand-supported hexanuclear Au(I) framework compromising a triangular Au3 core of which each apex is connected to an external Au(I) center has revealed a remarkable dual emission at room temperature. The emission bands display maxima centered at λem = 512 and 694 nm with Stokes shift of 19530 and 14410 cm-1 and are attributed to the radiative relaxation of two excited-states centered onto the central Au6 skeleton arising from 5dσ?→6pσ excitation. As suggested by the strikingly different dioxygen dependency of the relative intensity of the two emission bands, the observed dual emission can be tentatively attributed to the incomplete equilibration between two close-lying emissive excited states with singlet and triplet character, most likely due to slow intersystem crossing (ISC) process, yielding green fluorescence and red phosphorescence, respectively; this phenomenon is rarely observed in heavy element compounds. Based on theoretical calculations, these excited-states originated from two different substructures-luminophores of the molecular skeleton, mainly i) the Au3 core, and ii) one specific Au2 unit. Thus, the dual luminescence of 1 originates from the noteworthy inclusion of two luminophores within the overall molecular structure. Both solution and solid-state emission spectra show similar characteristics owing to the intramolecular nature of the suggested luminescence mechanism. Such luminophores can be envisaged as novel metalloligands to be incorporated in larger gold nanoclusters towards the development of intense luminescent molecular devices.