Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2 + 2] cycloadditions

Date

2019-07-25

Author

Erden, Kübra
Dengiz, Çağatay

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1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed efficiently under ambient conditions without any catalyst. The resulting products are structurally interesting push-pull chromophores and were investigated in the context of optoelectronic properties using UV/Vis spectroscopy, NMR studies, and computational chemistry

Subject Keywords

Organic Chemistry, Biochemistry, Drug Discovery

URI

https://hdl.handle.net/11511/42008

Journal

Tetrahedron Letters

DOI

https://doi.org/10.1016/j.tetlet.2019.06.046

Collections

Department of Chemistry, Article

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Citation Formats

K. Erden and Ç. Dengiz, “Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2 + 2] cycloadditions,” Tetrahedron Letters, pp. 1982–1985, 2019, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/42008.

Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2 + 2] cycloadditions

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Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2 + 2] cycloadditions