Exploring the role of neutral ligands in modulating the photoluminescence of samarium complexes with 1,1,1,5,5,5‐hexafluoro‐2,4‐pentanedione

Abstract Four eight‐coordinated luminescent samarium complexes of type [Sm(hfpd) 3 L 2 ] and [Sm(hfpd) 3 L′] [where hfpd = 1,1,1,5,5,5‐Hexafluoro‐2,4‐pentanedione L = tri‐octyl‐phosphine oxide (TOPO) and L′ = 1,10‐phenanthroline (phen), neocuproine (neoc) and bathocuproine (bathoc) were synthesized via a stoichiometrically controlled approach. This allows for precise control over the stoichiometry of the complexes, leading to reproducible properties. This investigation focuses on understanding the impact of secondary ligands on the luminescent properties of these complexes. Infrared (IR) spectra provided information about the molecular structures, whereas 1 H and 13 C nuclear magnetic resonance (NMR) spectra confirmed these structural details along with the coordination of ligands to trivalent Sm ion. The UV–vis spectra revealed the molar absorption coefficient and absorption bands associated with the hfpd ligand and photoluminescence (PL) spectroscopy demonstrated intense orange‐red emission (648 nm relative to 4 G 5/2 → 6 H 9/2 ) from the complexes. The Commission Internationale de l'Éclairage (CIE) triangles indicated that the complexes emitted warm orange red light with color coordinates ( x , y ) ranging from (0.62, 0.36) to (0.40, 0.27). The investigation of the band gap as well as color parameters confirms the utility of these complexes in displays and LEDs.