The detection of boron-containing compounds requires very expensive facilities and/or tedious sample pretreatments. In an effort to develop a convenient detection method for boronic acid derivatives, boron chelating-ligands were synthesized for use as fluorescent sensors. In this paper, the synthesis and properties of fluorescent sensors for boronic acid derivatives are reported.
The title compounds, 5-(dimethylamino)-2-[N-(4-methoxyphenyl)iminomethyl]phenyl}[N-(4-methoxyphenyl)-4-nitro-salicylaldiminato]palladium(II), [Pd(C14H11N2O4)(C16H17N2O)], (I), and [4-(diethylamino)-N-(4-methoxyphenyl)salicylaldiminato]2-[N-(4-methoxyphenyl)iminomethyl]-5-nitrophenyl}palladium(II) dichloromethane hemisolvate, [Pd(C14H11N2O3)(C18H21N2O2)]. 0.5CH(2)Cl(2), (II), both contain push-pull chromophores coordinated to Pd in a square-planar arrangement. In both compounds, the five-membered orthopalladated ring is essentially planar, while the coordinated six-membered ring is not. Deviations from a coplanar arrangement of the phenylene rings of the coordinated Schiff bases are observed in both (I) and (II) as a result of intramolecular steric interactions.