NO-induced adaptive aromaticity in furan, thiophene and selenophene

DOI: 10.1039/d5nj00492f Publication Date: 2025-03-08T22:41:16Z
ABSTRACT
Adaptive aromaticity (being aromatic in the lowest singlet and triplet states) is achieved in furan, thiophene and selenophene via the introduction of an NO group substituent due to its spin-acceptor ability.
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