Theoretical insights into excited-state hydrogen bonding effects and intramolecular proton transfer (ESIPT) mechanism for BTS system
J. M. Wang, Qiang Liu, Dapeng Yang
Abstract
Abstract In this work, N,N’-bis(salicylidene)-(2-(3′,4′-diaminophenyl)benzothiazole) (named as “BTS”) system was studied about its excited-state intramolecular proton transfer (ESIPT) process. The analyses about reduced density gradient (RDG) reveal the formation of two intramolecular hydrogen bonds in BTS system. Bond lengths and angles, infrared (IR) vibrations as well as frontier molecular orbitals (MOs) using TDDFT method indicate that the strength of hydrogen bond should be enhanced in the S 1 state. Particularly, hydrogen bond O1–H2···N3 undergoes larger variations compared with O4–H5···N6, which infers that hydrogen bond O1–H2···N3 may play a decisive role in the ESIPT process of BTS system. Given the two hydrogen bonds of BTS molecule, two types of potential energy curves have been constructed, which confirms that only single proton transfer process occurs due to lower energy barrier along with O1–H2···N3 rather than O4–H5···N6. This work not only presents a reasonable explanation for previous experiment, but also clarifies the specific ESIPT mechanism for BTS system.