Publication detail
Versatile photoluminescence behavior of polycyclic hydroxybenzimidazoles driven by intermolecular hydrogen bonding
YORDANOV, D. SMOLKA, R. VALA, M. WEITER, M. GEORGIEV, A.
Original Title
Versatile photoluminescence behavior of polycyclic hydroxybenzimidazoles driven by intermolecular hydrogen bonding
Type
journal article in Web of Science
Language
English
Original Abstract
Herein, the synthesis of polycyclic hydroxybenzimidazole based on 4-hydroxyphthalimide is presented and two isomeric structures are formed. The isomeric structures are capable of forming intermolecular hydrogen-bonded molecular associates. Hydroxybenzimidazole hydrogen-bonded organic frameworks have been shown to be sensitive to different solvent polarity, particularly in proton donor media, resulting in a blue shift in emission. The role of proton donor media has been evaluated using the binary mixture of acetonitrile/water and protonation by trifluoroacetic acid. The results show that by tuning the environment, the aggregation induced emission has appeared in the blue region and larger aggregates are formed compared to the less polar aprotic solvents. Under acidic conditions, the disruption of the hydrogen-bonded dimers was estimated, resulting in deep blue emission. This provides an opportunity to control the molecular associates and tune the optical behavior.
Keywords
Polycyclic benzimidazole; Non-covalent interactions; Hydrogen bonding; Photoluminescence; Organic frameworks
Authors
YORDANOV, D.; SMOLKA, R.; VALA, M.; WEITER, M.; GEORGIEV, A.
Released
13. 10. 2024
Publisher
ELSEVIER
Location
AMSTERDAM
ISBN
0925-3467
Periodical
OPTICAL MATERIALS
Year of study
157
Number
2
State
Kingdom of the Netherlands
Pages count
7
URL
BibTex
@article{BUT197039,
author="YORDANOV, D. and SMOLKA, R. and VALA, M. and WEITER, M. and GEORGIEV, A.",
title="Versatile photoluminescence behavior of polycyclic hydroxybenzimidazoles driven by intermolecular hydrogen bonding",
journal="OPTICAL MATERIALS",
year="2024",
volume="157",
number="2",
pages="7",
doi="10.1016/j.optmat.2024.116274",
issn="0925-3467",
url="https://www.sciencedirect.com/science/article/pii/S0925346724014575?via%3Dihub"
}