The orbital degeneracy of benzene rings is resolved by an asymmetric push‐pull system in 2,6‐bis(methylsulfonyl)aniline (BMeSA), in which the highest occupied molecular orbital (HOMO) is located at the 4‐position, while the lowest unoccupied mol...
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https://www.riss.kr/link?id=O118957238
2019년
-
1439-4235
1439-7641
SCI;SCIE;SCOPUS
학술저널
1581-1589 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
The orbital degeneracy of benzene rings is resolved by an asymmetric push‐pull system in 2,6‐bis(methylsulfonyl)aniline (BMeSA), in which the highest occupied molecular orbital (HOMO) is located at the 4‐position, while the lowest unoccupied mol...
The orbital degeneracy of benzene rings is resolved by an asymmetric push‐pull system in 2,6‐bis(methylsulfonyl)aniline (BMeSA), in which the highest occupied molecular orbital (HOMO) is located at the 4‐position, while the lowest unoccupied molecular orbital (LUMO) is located at a different position and has a nodal plane through the carbon atoms at the 1‐ and 4‐positions. Therefore, the π‐extension of BMeSA at the 4‐position reveals a strong overlap in the HOMO and a minimal overlap in the LUMO. Consequently, π‐extended BMeSA derivatives exhibit longer absorbance and emission wavelengths in the order of the electron‐donating abilities of their substituents at the 4‐position, which is based on a decrease in an absolute HOMO‐level‐dependent HOMO‐LUMO gap in accordance with the nodal arrangement. Positive fluorescent solvatochromism with polarity‐dependent decrease in fluorescent intensity was also observed. The biaryls exhibited more planar geometries in the excited state than in the ground state. The charge transfer mechanism, which can be described as node‐induced intramolecular charge transfer (NICT), differs from the planar intramolecular charge transfer (PICT) and twisted intramolecular charge transfer (TICT).
Degeneracy breaking: The orbital degeneracy of benzene rings is resolved by biased push‐pull system and asymmetric molecular orbital distribution. A linkage through the nodal plane provides HOMO‐level‐dependent tuning of the optical properties, a large dipole moment in the exited state, and positive solvatochromism in fluorescence with a large Stokes shift produced by a node‐induced intramolecular charge‐transfer mechanism.