Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles. - Wikidata - awgldk - TriplyDB

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

http://www.wikidata.org/entity/Q46921183

about

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.Siamese-Twin Porphyrin Origami: Oxidative Fusing and Folding.Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest hückel aromatic molecules.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.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 Reversible π-system switching of thiophene-fused thiahexaphyrins by solvent and oxidation/reduction

P2860

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P2860

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

http://www.wikidata.org/entity/Q46921183

description

2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

@wuu

2014年学术文章

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2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Diprotonated [28]hexaphyrins

@nl

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

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type

label

Diprotonated [28]hexaphyrins

@nl

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

@en

prefLabel

Diprotonated [28]hexaphyrins

@nl

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

@en

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Angewandte Chemie International Edition

P1476

Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles.

@en

P2093

Atsuhiro Osuka

http://www.w3.org/2001/XMLSchema#string

Dongho Kim

http://www.w3.org/2001/XMLSchema#string

Hirotaka Mori

http://www.w3.org/2001/XMLSchema#string

Naoki Aratani

http://www.w3.org/2001/XMLSchema#string

Shigeki Mori

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Shin-ichiro Ishida

http://www.w3.org/2001/XMLSchema#string

P2860

Reorganization energies of diprotonated and saddle-distorted porphyrins in photoinduced electron-transfer reduction controlled by conformational distortion.

Expanded porphyrin with a split personality: a Hückel-Möbius aromaticity switch.

Synthetic expanded porphyrin chemistry.

Aromaticity and photophysical properties of various topology-controlled expanded porphyrins.

Möbius aromaticity and antiaromaticity in expanded porphyrins.

Expanded porphyrins: intriguing structures, electronic properties, and reactivities.

Figure eights, Möbius bands, and more: conformation and aromaticity of porphyrinoids.

Three-level topology switching in a molecular Möbius band.

Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.

Perfluorinated meso-aryl-substituted expanded porphyrins.

P304

3427-3431

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scholarly article

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10.1002/ANIE.201400301

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13

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53

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Takayuki Tanaka

Tomohiro Higashino

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2014-02-24T00:00:00Z

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24615867

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