کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1341127 | 1500295 | 2005 | 6 صفحه PDF | دانلود رایگان |

We synthesized monodisperse oligo(9,10-anthryleneethynylene)s with pendant phenol residues at the 2- and 7-positions. The absorption maxima of oligomers shifted to longer wavelength with the degree of polymerization, suggesting a developed π-conjugation correlated with the chain length. The static magnetic susceptibility of the dimeric radical was measured using a SQUID magnetometer, and the 2J (J: spin coupling constant through the dianthrylacetylene unit) value of the dimeric radical was 34 cm−1, which agreed with the 2J value of the corresponding 2-substituted dimeric radical (31 cm−1). These large 2J values of the dimeric radicals can be explained from less steric hindrance between the side chain radicals and the backbone.
Monodisperse oligo(9,10-anthryleneethynylene)s A2a–A5a were synthesized. The 2J (J: spin coupling constant through the dianthrylacetylene unit) value of the dimeric radicals B2c (2J = 34 ± 1 cm−1) indicates less steric hindrance between the side chain radicals and the poly(9,10-anthryleneethynylene) backbone.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 24, Issues 16–17, 17 November 2005, Pages 2544–2549