کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5209756 | 1503076 | 2014 | 8 صفحه PDF | دانلود رایگان |
Poly(tetramethylsilarylenesiloxane) derivatives bearing benzo[1,2-b;4,5-bâ²]dithiophene (P1) and benzo[2,1-b;3,4-bâ²]dithiophene (P2) moieties were prepared via polycondensation of the corresponding disilanol monomers, that is, 2,6-bis(dimethylhydroxysilyl)benzo[1,2-b;4,5-bâ²]dithiophene (M1) and 2,7-bis(dimethylhydroxysilyl)benzo[2,1-b;3,4-bâ²]dithiophene (M2), respectively. It was deduced that P1 is a crystalline polymer while P2 is an amorphous one from the results of differential scanning calorimetry (DSC). Bathochromic and hyperchromic effects were observed in the absorption and fluorescence spectra when dimethylsilyl substituents were introduced on the benzo[1,2-b;4,5-bâ²]dithiophene and benzo[2,1-b;3,4-bâ²]dithiophene skeletons. The fluorescence quantum yields (ΦFs) were not improved by the introduction of dimethylsilyl groups onto the benzo[1,2-b;4,5-bâ²]dithiophene and benzo[2,1-b;3,4-bâ²]dithiophene skeletons, whereas the improvement in the ΦFs was remarkable in the case of poly(tetramethylsilarylenesiloxane) derivatives that possessed the corresponding fused benzene ring systems, i.e., poly(tetramethyl-2,6-silanthrylenesiloxane) and poly(tetramethyl-1,8-silphenanthrylenesiloxane).
Journal: Reactive and Functional Polymers - Volume 84, November 2014, Pages 60-67