| Autor: |
Klausen, Maxime, Dubois, Victor, Picard, Sébastien, Cueto Diaz, Eduardo, Daniel, Jonathan, Verlhac, Jean‐Baptiste, Blanchard‐Desce, Mireille |
| Předmět: |
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| Zdroj: |
Chemistry - A European Journal; 9/19/2024, Vol. 30 Issue 53, p1-8, 8p |
| Abstrakt: |
"Tandem" uncaging systems, in which a photolabile protecting group (PPG) is sensitized by an energy‐harvesting antenna, may increase the photosensitivity of PPGs by several orders of magnitude for two‐photon (2P) photorelease. Yet, they remain poorly accessible because of arduous multi‐step synthesis. In this work, we design efficient tandem uncaging systems by (i) using a convenient assembly of the building blocks relying on click chemistry, (ii) introducing H‐bonding induced proximity thus facilitating (iii) photoinduced electron transfer (PeT) as a cooperative mechanism. A strong two‐photon absorber electron‐donating quadrupolar antenna and various electron‐accepting PPGs (mDEAC, MNI or MDNI) were clicked stepwise onto a "tweezer‐shaped" pyrido‐2,6‐dicarboxylate platform whose H‐bonding and π‐stacking abilities were exploited to keep the antenna and the PPGs in close proximity. The different electron‐accepting ability of the PPGs led to dyads with wildly different behaviors. Whilst the MDNI and MNI dyads showed poor dark stability or no photo‐uncaging ability due to their too high electron‐accepting character, the mDEAC dyad benefited from optimum redox potentials to promote PeT and slow down charge recombination, resulting in enhanced uncaging quantum yield (Φu=0.38) compared to mDEAC (Φu=0.014). This unique combination resulted in large 2P photo‐sensitivity in the near‐infrared window (240 GM at 710 nm). [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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