Chemical syntheses and salient features of azulene-containing homo- and copolymers

Scholarly Works

• Shet, S. N.; Murthy, D. H. K.; Chandrappa, S.; Galbao, S. J.; Patil, M.; Shetti, V. S. Synthesis, Optoelectronic, and Photoelectrochemical Properties of an Azulene-Bridged Porphyrin Dimer. ACS Omega 2025. doi:10.1021/acsomega.5c05525
• Elwahy, A. H. M.; Shaaban, M. R.; Abdelhamid, I. A. New trends in the synthesis of azulene-fused heterocycles. Advances in Heterocyclic Chemistry; Elsevier, 2025; pp 263–330. doi:10.1016/bs.aihch.2025.01.001
• Starzak, K.; Tomal, W.; Chachaj-Brekiesz, A.; Galek, M.; Ortyl, J. Revealing the photoredox potential of azulene derivatives as panchromatic photoinitiators in various light-initiated polymerization processes. Polymer Chemistry 2024, 15, 2931–2948. doi:10.1039/d4py00275j
• Xiang, J.; Yang, Z.; Zhao, J.; Duan, C.; Wang, J.; Gao, X. Poly(vinyl azulene)s: An Emerging Class of Poly(vinyl arene)s. Macromolecules 2024, 57, 7516–7523. doi:10.1021/acs.macromol.4c00676
• Slon, E.; Slon, B.; Kowalczuk, D. Azulene and Its Derivatives as Potential Compounds in the Therapy of Dermatological and Anticancer Diseases: New Perspectives against the Backdrop of Current Research. Molecules (Basel, Switzerland) 2024, 29, 2020. doi:10.3390/molecules29092020
• Iwashina, T.; Nakagawa, H.; Sato, Y.; Hayami, R.; Yamamoto, K.; Gunji, T. Formation and characterization of palladium ethyl 2-aminoazulene-carboxylate complexes. Polyhedron 2024, 247, 116740. doi:10.1016/j.poly.2023.116740
• Wang, S. R. Direct Access to Functionalized Azulenes and Pseudoazulenes via Unconventional Alkyne Cyclization Reactions. Chemistry, an Asian journal 2023, 18, e202300244. doi:10.1002/asia.202300244
• Onuki, Y.; Yamazaki, K.; Masuda, Y.; Yakura, T.; Nambu, H. Ring‐Opening Cyclization of Spirocyclopropanes with Stabilized Phosphorus Ylides: Access to Indane and Azulene Skeletons. Advanced Synthesis & Catalysis 2023, 365, 2536–2544. doi:10.1002/adsc.202300021
• Razus, A. C. Azulene, Reactivity, and Scientific Interest Inversely Proportional to Ring Size; Part 1: The Five-Membered Ring. Symmetry 2023, 15, 310. doi:10.3390/sym15020310
• Razus, A. C. Dancing with Azulene. Symmetry 2022, 14, 297. doi:10.3390/sym14020297
• Hou, B.; Li, J.; Zhou, Z.; Tan, W. L.; Yang, X.; Zhang, J.; McNeill, C. R.; Ge, C.; Wang, J.; Gao, X. Incorporation of Electron-Rich Indacenodithiophene Units into the Backbone of 2,6-Azulene-Based Conjugated Polymers for Proton-Responsive Materials and p-Type Polymeric Semiconductors. ACS Materials Letters 2022, 4, 392–400. doi:10.1021/acsmaterialslett.1c00767
• Elwahy, A. H. M.; Abdelhamid, I. A.; Shaaban, M. R. Recent Advances in the Functionalization of Azulene Through Pd‐Catalyzed Cross‐Coupling Reactions. ChemistrySelect 2021, 6, 13664–13723. doi:10.1002/slct.202103357

Explore citations to this article at