Cyclophanes Containing Bowl-Shaped Aromatic Chromophores: Three Isomers of anti-[2.2](1,4)Subphthalocyaninophane

被引:7
|
作者
Liu, Quan [1 ]
Shimizu, Soji [2 ]
Kobayashi, Nagao [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai, Miyagi 9808578, Japan
[2] Kyushu Univ, Grad Sch Engn, Dept Chem & Biochem, Fukuoka 8190395, Japan
关键词
cyclophanes; ring-current effects; subphthalocyanines; transannular interactions; pi conjugation; MAGNETIC CIRCULAR-DICHROISM; PI-ELECTRON SYSTEMS; MCD SPECTROSCOPY; SUBPHTHALOCYANINES; PHTHALOCYANINE; ELECTROCHEMISTRY;
D O I
10.1002/anie.201411510
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The connection of bowl-shaped aromatic boron subphthalocyanines with anti-[2.2]paracyclophane resulted in the first observation of electronic communication between convex and concave surfaces. Three isomers of anti-[2.2](1,4)subphthalocyaninophane, described as concave-concave (CC), convex-concave (CV), and convex-convex (VV) according to the orientation of the subphthalocyanine units, were synthesized and characterized by various spectroscopic techniques, including (HNMR)-H-1, electronic absorption, fluorescence, and magnetic circular dichroism spectroscopy and Xray crystallography, together with molecular-orbital calculations. On going from the CC system to CV and further to VV, the Q band broadened and finally split as a result of through-space expansion of the conjugated systems, which were also reproduced theoretically.
引用
收藏
页码:5187 / 5191
页数:5
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