Theoretical Study of Dodecafluorophenylene-Based Superalkalides with Significantly High NLO Response

Areeg Sajjad; Sehrish Sarfaraz; Annum Ahsan; Imene Bayach; Malai Haniti S A Hamid; Nadeem S Sheikh; Khurshid Ayub

doi:10.1021/acsomega.3c05791

Theoretical Study of Dodecafluorophenylene-Based Superalkalides with Significantly High NLO Response

ACS Omega. 2023 Nov 21;8(48):45589-45598. doi: 10.1021/acsomega.3c05791. eCollection 2023 Dec 5.

Authors

Areeg Sajjad¹, Sehrish Sarfaraz¹, Annum Ahsan¹, Imene Bayach², Malai Haniti S A Hamid³, Nadeem S Sheikh³, Khurshid Ayub¹

Affiliations

¹ Department of Chemistry, COMSATS University Islamabad, Abbottabad Campus, Abbottabad 22060, KPK, Pakistan.
² Department of Chemistry, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
³ Chemical Sciences, Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, Gadong BE1410, Brunei Darussalam.

Abstract

Scientists are continuously trying to discover new approaches to develop materials with exceptional nonlinear optical responses. Compared with the single-ring Janus face compound (F₆C₆H₆), the three-ring Janus face compound (C₁₃H₁₀F₁₂) has a larger surface, where superalkali metals can be doped quite easily. Herein, the nonlinear optical response of Janus molecule dodecafluorophenylene (DDFP)-based superalkalides has been explored. The stability of the newly designed complexes is evident in the negative interaction energy values (ranging from -42.17 to -60.91 kcal/mol). The superalkalide nature of the complexes is corroborated through natural bond orbital (NBO) analysis, which shows negative charges on M₃. This feature is further confirmed through frontier molecular orbital (FMO) analyses showing the highest occupied molecular orbital (HOMO) density over superalkalis (M₃). The analysis also reveals that the H-L gap is reduced from 9.57 eV (for bare DDFP) to 2.11 eV for doped systems by adsorption of dopants on the DDFP surface. Moreover, the NLO response of the studied complexes is evaluated via static hyperpolarizabilities. The maximum value of first hyperpolarizability (β_o) among all of the designed compounds is for K₃-DDFP-K₃ (7.80 × 10⁴ au) at M06-2X/6-31+G(d,p) level of theory. The β_o is also rationalized through a two-level model. Furthermore, for β_vec, the projection of hyperpolarizability on the dipole moment is calculated. The comparable results of β_vec and β_o indicate that the charge transfer in the complexes is parallel to the molecular dipole moments. These compounds, besides providing a new entry into excess-electron compounds, will also pave the way for the design and synthesis of further novel NLO materials.