Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
about
Expanded porphyrins: intriguing structures, electronic properties, and reactivities.[32]π Fused Core-Modified Heptaphyrin with Möbius Aromaticity.Topology switching in [32]heptaphyrins controlled by solvent, protonation, and meso substituents.Conformational change from a twisted figure-eight to an open-extended structure in doubly fused 36π core-modified octaphyrins triggered by protonation: implication on photodynamics and aromaticity.Structural, Photophysical, and Magnetic Circular Dichroism Studies of Three Rigidified meso-Pentafluorophenyl-Substituted Hexaphyrin Analogues.ESI-MS/MS of expanded porphyrins: a look into their structure and aromaticity.Multifaceted [36]octaphyrin(1.1.1.1.1.1.1.1): deprotonation-induced switching among nonaromatic, Möbius aromatic, and Hückel antiaromatic species.Understanding the molecular switching properties of octaphyrins.Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest hückel aromatic molecules.Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.Deprotonation induced formation of Möbius aromatic [32]heptaphyrins.Relevance of the DFT method to study expanded porphyrins with different topologies.Internally 2,5-Thienylene-Bridged [46]Decaphyrin: (Annuleno)annulene Network Consisting of Möbius Aromatic Thia[28]hexaphyrins and Strong Hückel Aromaticity of its Protonated Form.meso-Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology.Understanding conductivity in molecular switches: a real space approach in octaphyrins.Möbius-Hückel topology switching in an expanded porphyrin cation radical as studied by EPR and ENDOR spectroscopy.Modulation of dual electronic circuits of [26]hexaphyrins using internal aromatic straps.Switchable π-electronic network of bis(α-oligothienyl)-substituted hexaphyrins between helical versus rectangular circuit† †Electronic supplementary information (ESI) available. CCDC 1425255. For ESI and crystallographic data in CIF or other electroReversible π-system switching of thiophene-fused thiahexaphyrins by solvent and oxidation/reduction
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P2860
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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name
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@en
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@nl
type
label
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@en
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@nl
prefLabel
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@en
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@nl
P50
P356
P1476
Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
@en
P2093
Jae-Yoon Shin
Yasuo Tanaka
P304
P356
10.1021/JA909744Z
P407
P577
2010-03-01T00:00:00Z