five

Synthesis of Carbazole-Based Selenaporphyrin via Annulation

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Synthesis_of_Carbazole_Based_Selenaporphyrin_i_via_i_Annulation/2447887
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Cu(I)-mediated alkoxylation of doubly 1,3-butadiyne-bridged carbazole dimer 1, followed by acid-catalyzed cyclization, provided furan-bridged carbazole dimer 3, while annulation reaction of 1 with selenium in the presence of hydrazine monohydrate provided selenophene-bridged carbazole dimer 5a. Oxidation of isophlorin 5a afforded carbazole-based selenaporphyrin 5b, which possessed distinct aromaticity and produced intensified and red-shifted absorption bands in the near-IR region.
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2016-02-20
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