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• W2550249769 endingPage "1051" @default.
• W2550249769 startingPage "1048" @default.
• W2550249769 abstract "Abstract Sequential N ‐alkylations of tetrabenzotetraaza[8]circulene provided mono‐, di‐, tri, and tetra‐ N ‐alkylated products in a controlled manner. Curiously, only opp isomer was obtained as a di‐ N ‐alkylated product. Upon increase of the N ‐alkyl groups, the absorption and emission spectra exhibit continuous red‐shifts, and the excited‐state lifetimes become shortened, probably because of increased steric congestion at the nitrogen atoms that causes the central core to deviate from planarity. Mixed N ‐substituted [8]circulenes have been also prepared." @default.
• W2550249769 created "2016-11-30" @default.
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• W2550249769 date "2016-11-25" @default.
• W2550249769 modified "2023-10-14" @default.
• W2550249769 title "Sequential<i>N</i>-Alkylations of Tetrabenzotetraaza[8]circulene as a Tool To Tune Its Optical Properties" @default.
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• W2550249769 doi "https://doi.org/10.1002/cplu.201600537" @default.
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