New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction

The design and synthesis of novel charge‐transfer (CT) complexes are of interest for fundamental chemistry and applications to materials science. In addition to the recently described first CT complex with both electron acceptor (A) and donor (D) groups belonging to the 1,2,5‐thiadiazole series (1; A: 4‐nitro‐2,1,3‐benzothiadiazole; D: 4‐amino‐2,1,3‐benzothiadiazole), herein novel CT complexes2and3with 1,2,5‐thiadiazoles as both A (4,6‐dinitro‐2,1,3‐benzothiadiazole and [1,2,5]thiadiazolo[3,4‐c][1,2,5]thiadiazole) and D (4‐amino‐2,1,3‐benzothiadiazole) were synthesized. The series is completed by complex4with [1,2,5]thiadiazolo[3,4‐c][1,2,5]thiadiazole as A and phenoxatellurine as D. Structures of complexes2–4were characterized by single‐crystal X‐ray diffraction (XRD), as well as solution and solid‐state UV/Vis spectroscopy. Thermodynamics of their formation were obtained by density functional theory (DFT) calculations, their bonding situations were analyzed by quantum theory of atoms in molecules (QTAIM) calculations and dimer model energies of interactions quantified in the framework of the Hirshfeld surface (HS) analysis. With DFT calculations, the largest value of CT between D and A was found for complex2, with 0.027 e in the XRD structure and 0.150 e in the optimized structure in MeCN. In the UV/Vis spectra, theλ_maxof the CT bands of2–4varied in the rangeλ=517–705 nm. Model energy calculations for1–4revealed the importance of both dispersion interactions and hydrogen bonding between D and A as contributors to CT in the crystalline state. In an attempt to enlarge the CT value with bis[1,2,5‐thiadiazolo][3,4‐b;3′,4′‐e]pyrazine as A and 4‐amino‐2,1,3‐benzoselenadiazole as D, an unprecedented 1:1 addition reaction was observed upon formation of a C−N bond between atom C7 of D and pyrazine atom N4 of A, accompanied by hydrogen atom transfer from C7 to another pyrazine atom N8 (compound5). According to DFT calculations, the reaction is a multistep process featuring diradical intermediates and hydrogen atom intramolecular migration over four positions. Molecular and crystal structures of5(solvate with toluene) were elucidated by XRD and the crystal structure revealed a rather unusual porous framework.