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Molecular Physics
An International Journal at the Interface Between Chemistry and Physics
Volume 119, 2021 - Issue 3
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Research Articles

Uncovering photo-excited intramolecular charge transfer and ESIPT mechanism for 5,5′-(9,9-dioctyl-9H-fluorene-2,7-diyl) bis(2-benzo[d]thiazol-2-yl) phenol compound

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Article: e1805130 | Received 07 Apr 2020, Accepted 29 Jul 2020, Published online: 11 Aug 2020
 

Abstract

In view of their facile synthetic routes and remarkable photo-induced stabilities, excited state intramolecular proton-transfer (ESIPT)-vibrant luminous materials have drawn more and more attention. In this work, we mainly focus on the photo-induced excitation behaviours, including excited state hydrogen bonding interactions and ESIPT reaction of a new 5,5′-(9,9-dioctyl-9H-fluorene-2,7-diyl)-bis(2-benzo[d]thiazol-2-yl) phenol molecule theoretically. To be consistent with the previous experiment, we name this molecule as IIa. Using molecular electrostatic potential (MEP), we explored the dual intramolecular hydrogen bonding interactions in IIa form. Then on the level of chemical geometries and infrared (IR) spectra, we confirmed that the double hydrogen bonds should be enhanced upon photoexcitation. Probing into charge reorganisation, we found that hydrogen proton does prefer to be attracted by enhanced electronic densities around N3 and N6. Combining potential energy surfaces (PESs) and electronic spectra, the excited state intramolecular single proton-transfer (ESISPT) behaviour could be verified for IIa although it owns two hydrogen bonds.

GRAPHICAL ABSTRACT

Acknowledgements

This work was supported by the Key Scientific Research Project of Colleges and Universities of Henan Province of China (16B140002 and 18A140023) and Science and Technology Research Project of Henan Province (172102210391).

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by the Key Scientific Research Project of Colleges and Universities of Henan Province of China [grant number 16B140002], [grant number 18A140023] and Science and Technology Research Project of Henan Province [grant number 172102210391].

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