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DOI: 10.1055/a-2760-7252
Synthesis and Characterization of Novel Cyclopenta[c]pyrans Functionalized with Phenothiazine or Terpyridine Units
Authors
This work was supported by the projects: EVOLUTION funded by European Union – NextGenerationEU and the Romanian Government, under National Recovery and Resilience Plan for Romania, contract no 760033/23.05.2023, cod PNRR-C9-I8-CF16/2022, through the Romanian Ministry of Research, Innovation and Digitalization, within Component 9, Investment I8 and Brâncuși, cod PN-IV-P8-8.3-PM-RO-FR-2024-0071.

Abstract
This work reports the synthesis and structural characterization of novel derivatives incorporating the cyclopenta[c]pyran core and either a phenothiazine or a 2,2′:6′,2″-terpyridine unit. The coupling between the cyclopenta[c]pyran moiety and the heterocyclic unit was achieved through a Suzuki–Miyaura cross-coupling reaction. The compounds were analyzed by NMR, UV–vis, and fluorescence spectroscopy, while the molecular structure of the phenylcyclopenta[c]pyranyl-biphenylterpyridine derivative was confirmed by single-crystal X-ray diffraction.
Keywords
Cyclopenta[c]pyrans - Terpyridines - Phenothiazines - UV–vis - Fluorescence - Molecular structuresPublication History
Received: 29 September 2025
Accepted after revision: 01 December 2025
Accepted Manuscript online:
02 December 2025
Article published online:
22 December 2025
© 2025. Thieme. All rights reserved.
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