“…For these applications, the most general and important strategy for designing fluorescent materials based on the pyrene chromophore is to introduce substituents at the 1-, 3-, 6-, and 8-positions in the pyrene. For instance, it is widely known that the introduction of phenyl − and ethynyl groups − or trimethylsilyl (TMS) ,− and trimethylsilylmethyl (TMSM) groups at the 1-, 3-, 6-, and 8-positions in pyrene expand the π-system and increase the oscillator strength, resulting in dramatic improvements in the photoluminescence (PL) properties, especially in the fluorescence quantum yield. In addition, various functional groups such as carbonyl groups have been also used to modify the PL properties as well as the mechanisms of the PL in pyrene. − Furthermore, these pyrene dyes have often been introduced into sophisticated structures such as spiro skeletons, polymers, − cyclophanes, , calix arenes, , and inorganic matrixes , to obtain various desired functions.…”