Fluorescence spectroscopy as an analytical tool for various applications as well as fluorescence probes showing a sensitive behavior towards their microenvironmental properties have experienced an increasing interest in research in the last decades. Recently our group has contributed to this field of interest by introducing a novel mechanism where a planarization in the excited state occurs leading to an advantageous allowed emission. Here, we provide an overview of intramolecular charge transfer states where a rotation in the excited state causes a high sensitivity for microenvironmental changes. Furthermore, effects which influence the surroundings of the fluorophores are described in detail. Recent results where twisted intramolecular charge transfer (TICT) and aggregation‐induced emission (AIE) effects were combined are described and a promising outlook for further research progress is provided.