Lowering LUMO, reducing bandgap, and increasing aromaticity by modifying one of the substituents of a lesser-known pro-aromatic PAH, Fluorene-fused Phenalene, via a modular synthesis @ChemCommun 2026 Pioneering Investigator @sak71477 https://t.co/SpVfuCrJFD
Lowering LUMO, reducing bandgap, and increasing aromaticity by modifying one of the substituents of a lesser-known pro-aromatic PAH, Fluorene-fused Phenalene, via a modular synthesis @ChemCommun 2026 Pioneering Investigator @sak71477 https://t.co/SpVfuCrJFD
Following our N-annulated indenofluorene motif, we designed and synthesized N-annulated [5]helicene as another six-ringed azepine-fused polycycle, alongside its dibenzo-fused variant to serve as hole-transporting materials @JOC_OL#OrgLett@Hemonta29837649 https://t.co/FE7R9JZbEF
Azulene is an isomer of Naphthalene. Likewise, N-annulated Indenofluorene is just synthesized by @Hemonta29837649 as an isomer of the N-annulated Perylene for materials science: Synthesis, Properties, Antiaromaticity, and Charge-Transport #OrgLett@JOC_OL
https://t.co/2dzYVQmkmP
Combining a widely recognized and a lesser-known rule of Aromaticity to explain the Fine-tuned Antiaromaticity of s-indacene in larger 4npi motifs: Design, Syntheses, Theory, Field-Effect Transistors. @JOC_OL@ACSPublications@Hemonta29837649@PSenanayak
https://t.co/ZVn6AW1BZg