DIB-ET was synthesized in our laboratory according to the previously reported method by our research group. 12
Bromobenzene, o-bromoanisole, p-bromoanisole, o-bromotoluene, p-bromotoluene, p-chloroanisole, p-chlorotoluene,
N,Ndiisopropylethylamine (DIPEA), iodobenzene,
p-iodoanisole and p-iodotoluene were purchased from Tokyo Chemical Industries (Tokyo). Chrolobenzene, tris{tris[3,5-bis(trifluoromethyl)phenyl]phosphine}palladium (super stable Pd catalyst),
1,4-dioxane, and o-iodoanisole were from Wako (Tokyo). m-Bromoanisole, copper (I) iodide (CuI) and
acetonitrile were from Kanto Chemical (Tokyo). m-Bromotoluene was purchased from Sigma (St. Louis, MO). All of the used chemicals were of the highest purity and quality available, while the purities of the tested aryl halide were 98%, excluding
Bromobenzene (99%) and p-bromoanisole (97%).
The synthesis and characterization of the aryl halides authentic derivatives of DIB-ET are described in Supporting Information.
Aryl halides standard solutions, DIB-ET (3.0 mM), super stable Pd (2.5 mM), CuI (0.5 mM) and DIPEA (50 mM) reagent solutions were prepared in dioxane.
Yasaka N., Kishikawa N., Higashijima T., Ohyama K, & Kuroda N. (2018). The Utility of Sonogashira Coupling Reaction for the Derivatization of Aryl Halides with Fluorescent Alkyne. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 34(10).