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Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin
Chemical Communications ( IF 4.9 ) Pub Date : 2017-12-19 00:00:00 , DOI: 10.1039/c7cc08754c Michał J. Białek 1, 2, 3, 4 , Lechosław Latos-Grażyński 1, 2, 3, 4
Chemical Communications ( IF 4.9 ) Pub Date : 2017-12-19 00:00:00 , DOI: 10.1039/c7cc08754c Michał J. Białek 1, 2, 3, 4 , Lechosław Latos-Grażyński 1, 2, 3, 4
Affiliation
The incorporation of an azulene bridge into an aromatic hexaphyrin framework allows manipulating π-electron delocalization pathways. The palladium(II) complex undergoes hydroxyl-triggered azulene contraction or isomerization to an oxynaphthalene unit, transforming the hexaphyrin framework into meso-linked carbaporphyrins. This converts the 26π-electron pathway into the 18π one.
中文翻译:
芳香开关通过在薁变换薁桥接A,d-dithiahexaphyrin
将氮杂环戊二烯桥结合到芳族六卟啉骨架中允许操纵π电子离域化途径。钯(II)配合物经历羟基触发的氮杂苯缩合或异构化为氧萘单元,将六卟啉骨架转化为内消旋碳杂卟啉。这将26π电子路径转换为18π电子路径。
更新日期:2018-02-15
中文翻译:
芳香开关通过在薁变换薁桥接A,d-dithiahexaphyrin
将氮杂环戊二烯桥结合到芳族六卟啉骨架中允许操纵π电子离域化途径。钯(II)配合物经历羟基触发的氮杂苯缩合或异构化为氧萘单元,将六卟啉骨架转化为内消旋碳杂卟啉。这将26π电子路径转换为18π电子路径。