Boron/nitrogen substituted the staggered hetero-dimers: Fascinating intermolecular charge-transfer and large NLO responses

Abstract

Recently, the structure-property relationships of an attractive isomeric radical 1 (Phys. Chem. Chem. Phys., 2016, 18, 29041–29044) with famous phenalenyl (PLY) was investigated. Can PLY and 1 form stable π-dimers? The single point energy scan result shows that the staggered π-dimer (2) has the lowest energy. In order to explore intermolecular charge-transfer and nonlinear optical property, two π-dimers (2a and 2b by boron and nitrogen atoms substituting the central carbon atoms of 2) are designed. 2 has smaller intermolecular charge-transfer (0.020) and the first hyperpolarizability (βtot, 3.18 × 102 au). However, boron and nitrogen substitution effect can greatly enhance intermolecular charge-transfer (0.215 for 2a and 0.181 for 2b) and the βtot values (6.32 × 103 for 2a and 6.80 × 103 for 2b). Interestingly, the βtot values of 2a and 2b are close to each other, but their βz components and the NBO charge analysis show that 2a and 2b have opposite direction of charge transfer, which can be well explained by the difference of the dipole moment component (Δμz) between the ground and the excited states. Further, the first hyperpolarizability density study clearly substantiates the difference in their βzzz values: negative contribution for 2a is much larger than positive contribution, while the first hyperpolarizability density for 2b shows much larger positive contribution. Thus, the primary component of βzzz is negative value for 2a and βzzz is positive value for 2b. Combining with the frontier molecular orbital (FMO) and the electron density difference map (EDDM), intermolecular charge-transfer transition from B substituted fragment to N substituted fragment for 2a and 2b is concluded. The significant structure-property relationships in present π-dimers are beneficial for further theoretical and experimental investigations of high-performance nonlinear optical materials.