Abstract
AbstractIn biological imaging, red‐to‐infrared emissive dyes facilitate direct visualization of molecular interactions, through deep tissue penetration, along with minimal tissue damage. This work uses simple systems based on a single dye‐doped polymeric thin film for distributed feedback and random lasing investigations. As active compounds, novel push‐pull luminescent diphenylaminofluorene derivatives are used, functionalized with different acceptor groups. Integration of such luminescent dyes with a transparent polymeric medium allows fabrication of real‐time lasing tunability in the first biological window (650–950 nm). The observed spectral tuning of 150 nm is a groundbreaking value obtained in a single‐dye system.
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