Design, synthesis, and reaction of π-extended coumarin-based new caged compounds with two-photon absorption character in the near-IR region - Université de Rennes Accéder directement au contenu
Article Dans Une Revue Chemistry Letters Année : 2016

Design, synthesis, and reaction of π-extended coumarin-based new caged compounds with two-photon absorption character in the near-IR region

Résumé

Novel π-extended coumarin-based chromophores were designed with two-photon absorption (TPA) character in the near-IR region. Caged benzoates with a TP-responsive chromophore were synthesized, and their TP-uncaging reactions were conducted under near-IR light. The 6,7-dimethoxy-substituted derivative had a high TPA cross-section of 69 GM at 740 nm. The 7-methoxy-substituted derivative showed a high TPA uncaging efficiency with a TPA efficiency of 3.4 GM at 710 nm. © 2016 The Chemical Society of Japan.

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Chimie
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Dates et versions

hal-01398035 , version 1 (24-11-2016)

Identifiants

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Y. Chitose, Manabu Abe, K. Furukawa, Claudine Katan. Design, synthesis, and reaction of π-extended coumarin-based new caged compounds with two-photon absorption character in the near-IR region. Chemistry Letters, 2016, 45 (10), pp.1186--1188. ⟨10.1246/cl.160586⟩. ⟨hal-01398035⟩
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