Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest hückel aromatic molecules.
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Multifaceted [36]octaphyrin(1.1.1.1.1.1.1.1): deprotonation-induced switching among nonaromatic, Möbius aromatic, and Hückel antiaromatic species.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.[62]Tetradecaphyrin and Its Mono- and Bis-Zn(II) Complexes.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 electro
P2860
Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest hückel aromatic molecules.
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2015年の論文
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Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@en
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@nl
type
label
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@en
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@nl
prefLabel
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@en
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@nl
P2093
P2860
P356
P1476
Stable [48]-, [50]-, and [52]d ...... est hückel aromatic molecules.
@en
P2093
Atsuhiro Osuka
Takanori Soya
Woojae Kim
P2860
P304
P356
10.1002/CHEM.201500650
P407
P50
P577
2015-04-13T00:00:00Z