Evidence map›Paper›PMID 42907927›Full record

ArticleBMC chemistry2026

A novel pyridine-functionalized naphthoxazine: thermal stability, proton and metal ion-responsive optical sensing, and biological activity with DFT validation.

Abdulsalam Mahdy, Jalal A Zahra, Randa N Haddadin, Violet Kasabri, Murad A AlDamen

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Article in BMC chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Abdulsalam MahdyChemistry Department, Faculty of Education and Science, Albaydha University, Rada'a, Albaydha, Yemen. abdualsalam735@gmail.com.ORCID https://orcid.org/0009-0009-2096-074X
Jalal A ZahraChemistry Department, School of Science, The University of Jordan, Amman, 11942, Jordan.
Randa N HaddadinDepartment of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy, The University of Jordan, Amman, 11942, Jordan.
Violet KasabriDepartment of Biopharmaceutics and Clinical Pharmacy, School of Pharmacy, The University of Jordan, Amman, 11942, Jordan.
Murad A AlDamenChemistry Department, School of Science, The University of Jordan, Amman, 11942, Jordan. maldamen@ju.edu.jo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Designing multifunctional polymers that combine thermal stability, selective optical response, and biological activity remains a key challenge in smart materials development. Herein, we report a novel pyridine-functionalized naphthoxazine monomer (Py-NZ) synthesized via a one-pot Mannich condensation and fully characterized by 1D/2D NMR, FTIR, and HRMS. DFT calculations confirmed the optimized geometry, showing excellent agreement with experimental data (RMSD = 0.018 Å; mean IR error = 0.43%), validating its extended π-conjugated structure. Thermogravimetric analysis of the cured Poly(Py-NZ) revealed outstanding thermal stability, with a char yield of 69% at 800 °C and a limiting oxygen index (LOI) of 45.1, indicating strong flame-retardant potential. UV-Vis and fluorescence spectroscopy demonstrated that metal coordination significantly modifies the optical behavior. Among the tested metal ions, Zn²⁺ induced a marked fluorescence enhancement due to its d¹⁰ configuration, which suppresses nonradiative decay and favors radiative emission. Py-NZ also exhibited strong acid-responsive fluorescence: high HCl concentrations quenched emission via protonation-induced nonradiative pathways, while lower acidity restored intensity, confirming its dual-responsive chemosensing capability for both metal ions and protons. Biological evaluation showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli, with the protonated form exhibiting enhanced activity against Gram-positive bacteria (MIC = 15.6 µg/mL). In DPPH antioxidant assays, all compounds displayed dose-dependent reductive activity comparable to ascorbic acid, with the Zn²⁺-coordinated complex showing the highest potency of nanomolarity radical scavenging affinities (IC₅₀ = 0.15 ± 0.01 vs. 0.041 ± 0.0062 for ascorbic acid). Overall, this work establishes a versatile platform for naphthoxazine-based multifunctional materials with potential applications in flame-retardant coatings, optical sensing, and biomedical fields.

Indexed as

Biological activityDFTFluorescence chemosensorMetal coordinationNaphthoxazinePyridine

Identifiers

PMID42907927
PMCPMC13689125

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