Laverick, RJ orcid.org/0000-0003-1840-871X, Zhang, N, Reid, E et al. (3 more authors) (2021) Solution processible Co(III) quinoline-thiosemicarbazone complexes: synthesis, structure extension, and Langmuir-Blodgett deposition studies. Journal of Coordination Chemistry, 74 (1-3). pp. 321-340. ISSN: 0095-8972
Abstract
Seven readily synthesized 8-quinoline-4-R-3-thiosemicarbazone ligands [where R = phenyl (L1H), 4-fluorophenyl (L2H), 4-iodophenyl (L3H), 4-nitrophenyl (L4H), 4-carboxyphenyl (L5H), 3-picolyl (L6H), and octadecyl (L7H)], and their corresponding Co(III) coordination complexes, [Co(L)2]BF4, have been synthesized and characterized. Crystallographic analysis of the complexes revealed that the substituents significantly alter solid-state supramolecular network topologies. The solution processability of these complexes was confirmed by incorporating a long carbon alkyl-chain into the ligand (L7H) and immobilizing the complex onto quartz slides using Langmuir-Blodgett deposition. The facile and modular synthesis of these thiosemicarbazone-based ligands coupled with the potential to exploit multiple applications makes these compounds excellent candidates for functional supramolecular materials.
Metadata
| Item Type: | Article | 
|---|---|
| Authors/Creators: | 
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| Copyright, Publisher and Additional Information: | © 2021 Informa UK Limited, trading as Taylor & Francis Group. This is an author produced version of an article published in Journal of Coordination Chemistry. Uploaded in accordance with the publisher's self-archiving policy. | 
| Keywords: | Thiosemicarbazone; cobalt (III); supramolecular materials; Langmuir-Blodgett; structure extension | 
| Dates: | 
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| Institution: | The University of Leeds | 
| Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Physical Chemistry (Leeds) | 
| Depositing User: | Symplectic Publications | 
| Date Deposited: | 11 Jan 2023 17:03 | 
| Last Modified: | 13 Aug 2025 14:56 | 
| Published Version: | http://dx.doi.org/10.1080/00958972.2021.1879384 | 
| Status: | Published | 
| Publisher: | Taylor and Francis Group | 
| Identification Number: | 10.1080/00958972.2021.1879384 | 
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:194929 | 

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