Poly(tetramethyl-1,6-silpyrenylenesiloxane) derivative with phenyl groups on pyrenylene moieties (P1) was prepared via polycondensation of disilanol monomer, i.e. 1,6-bis(dimethylhydroxysilyl)-3,8-diphenylpyrene (M1). P1 exhibited the very high glass transition temperature (T (g)) of 191 A degrees C. The temperature at 5% weight loss (T (d5)) of P1 was 482 A degrees C, indicating the relatively good thermostability of P1. P1 exhibited the bathochromic effect in the absorption and fluorescence spectra, indicating the expansion of pi-conjugation by introducing phenyl groups onto pyrene skeleton as well as the sigma-IEuro and sigma*-IEuro* conjugation between pyrene and silyl moieties. In addition, P1 exhibited relatively weak excimer emission because of the inhibition of the excimer formation of pyrene skeleton by introduction of bulky phenyl groups onto pyrene skeleton. The fluorescence quantum yields (I broken vertical bar(F)s) of M1 and P1 in chloroform were determined to be 0.46 and 0.37, respectively. It was revealed that M1 and P1 exhibited the higher fluorescence intensity than 1,6-diphenylpyrene, owing to the effect of the introduction of silyl moieties onto pyrene skeleton.