Multicomponent synthesis of stereogenic-at-boron fluorophores (BOSPYR) from boronic acids, salicylaldehydes, and 2-formylpyrrole hydrazones

Date

2024-01-01

Author

Bayer, Ezgi
Batool, Sania
ŞAHİN, Ertan
Yıldırım, Erol
Işık, Murat
Tanyeli, Cihangir

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This work describes one-step syntheses of various stereogenic-at-boron fluorochromes (BOSPYR) via multicomponent reactions involving readily accessible boronic acids, salicylaldehydes, and 2-formylpyrrole hydrazones. The dyes absorb and emit in the visible region of the electromagnetic radiation, and are characterized by large Stokes shifts (2850-4930 cm−1) with weak fluorescence emissions (Φfl: 1.5-9.1%). Notably, the dimmed fluorescence of BOSPYRs recovers upon transition to viscous media (21-fold for 1a). The representative compound 1a exhibits clear Cotton effects with dissymmetry factors of ca. |gabs| ∼ 1.9 × 10−3 in the visible region, indicating efficient asymmetry induction to the chromophore. The X-ray molecular structure of 1a shows that the chromophore deviates from planarity by 17.2°, which may contribute significantly to the inherent chirality of the fluorophore. A computational examination of excited states by time-dependent density functional theory (TD-DFT) identifies the emission mechanism as arising from a locally-excited (LE) state.

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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85212058392&origin=inward
https://hdl.handle.net/11511/112899

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Department of Chemistry, Article