Linkage length dependence of intramolecular photoinduced electron transfer reactions in aromatic donor-viologen acceptor molecules linked by polymethylene bridges
Linkage length dependence of intramolecular photoinduced electron transfer reactions in aromatic donor-viologen acceptor molecules linked by polymethylene bridges
复制标题
通过多亚甲基桥连接的芳香族供体-紫精受体分子中分子内光诱导电子转移反应的键长依赖性
DOI:
10.1021/jp981131d
复制
发表时间:
1998
影响因子:
3.3
通讯作者:
Soo Yeon Lee
中科院分区:
文献类型:
--
作者:
J. Park;Bichna Lee;Soo Yeon Lee
The intramolecualr charge transfer (CT) complex formation and photoinduced electron-transfer reactions in aromatic donor−viologen acceptor dyad systems linked by polymethylene linkage (-(CH2)n-) have been studied. The donors and the numbers of methylene unit in the linkages are 1-naphthoxyl with n = 3, 6, 8, and 10, 2-naphthoxyl with n = 3−10 and 12, and 2-dibenzofuranoyl with n = 3, 6, 8, and 10. The formation constants of the intramolecular CT complexes (Kint) were determined from the absorbance of CT absorption by using the absorptivities of the complexes determined from the intermolecular complexation between the model donor compounds, the 1-aryloxy-3-aminopropanes, and dimethyl viologen. The Kint values depend little on the length of the linkage and are about 0.2 for 1-naphthol and 2-naphthol derivatives, and 0.6 for dibenzofuranoyl derivatives. The addition of β-CD disrupts the formation of the intramolecular CT complexes. The 1:1 association constants of the dyad molecules with β-CD (KCD) were esti...