Abstract
A key discovery of this study is the strong correlation (r = 0.96) between excitation and emission maxima across chemically distinct clusteroluminogens. All 157 evaluated peaks fall along a single regression line (Ex = 0.844 Em - 12 nm), a pattern that was not valid for conventional fluorophores. This suggests a general principle of clusteroluminescence. We show that in lignocellulosic materials, peak positions reflect chemical interactions: isolated lignin and cellulose showed short excitation and emission wavelengths, while native wood exhibited longer wavelengths. Fungal or photoinduced degradation led to a further red-shift. These effects are attributed to increased molecular heterogeneity, reducing the effective energy gap within the lignocellulosic complex. We conclude that the spectral position reflects the degree of molecular interaction rather than the chemical structure of individual molecules. It may serve as a novel analytical parameter for assessing purity and degradation in a wide range of polymers.