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Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines

Pagidi, S and Kalluvettukuzhy, NK and Thilagar, P (2020) Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines. In: Inorganic Chemistry, 59 (5). pp. 3142-3151.

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Official URL: https://doi.org/10.1021/acs.inorgchem.9b03446

Abstract

A donor-π-acceptor strategy is being well exploited in several fields in view of their robust optical properties. However, the impact of branching in quadrupolar [A-(D)2] and octupolar [A-(D)3] molecules in comparison to parent dipolar (A-D) molecules on the delayed fluorescence and phosphorescence properties is seldom explored. We have presented herein the distinct and contrasting optical properties of a tridurylborane core bearing -NH2 (1-3) and -NMe2 (4-6) donor moieties, wherein the number of donors is increased systematically. Because of propeller molecular architecture, the donor and acceptor are weakly coupled, and the frontier molecular orbitals are spatially localized. All of the compounds show delayed fluorescence under ambient conditions and persistent phosphorescence at low temperature. Solvent-dependent studies and temperature-dependent luminescence measurements established that quadrupolar (2 and 5) and octupolar (3 and 6) compounds underwent symmetry breaking in the excited state. Curiously, delayed fluorescence and phosphorescence spectra are found to be blue-shifted and follow the same trend as the fluorescence upon an increase in the branches. The highest quantum yield was observed for dipolar compounds. Besides, the phosphorescence lifetime decreases with an increase in the number of branches. These interesting experimental observations are further supported by quantum-mechanical calculations

Item Type: Journal Article
Publication: Inorganic Chemistry
Publisher: American Chemical Society
Additional Information: The copyright for this article belongs to the American Chemical Society
Keywords: Digital Human Model; Functional reach; reach envelope; reach simulation; standing reach
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 01 Feb 2023 09:52
Last Modified: 01 Feb 2023 09:52
URI: https://eprints.iisc.ac.in/id/eprint/79691

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