Diindenothienoacene–tetrathiafulvalene redox systems

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Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations.On the association of neutral and cationic tris(tetrathiafulvaleno)dodecadehydro[18]annulenes.Expanded Indacene-Tetrathiafulvalene Scaffolds: Structural Implications for Redox Properties and Association Behavior.

P2860

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P2860

Diindenothienoacene–tetrathiafulvalene redox systems

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http://www.wikidata.org/entity/Q57909586

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article

@en

im Jahr 2015 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована у 2015

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name

Diindenothienoacene–tetrathiafulvalene redox systems

@en

Diindenothienoacene–tetrathiafulvalene redox systems

@nl

type

Item

label

Diindenothienoacene–tetrathiafulvalene redox systems

@en

Diindenothienoacene–tetrathiafulvalene redox systems

@nl

prefLabel

Diindenothienoacene–tetrathiafulvalene redox systems

@en

Diindenothienoacene–tetrathiafulvalene redox systems

@nl

P1476

Diindenothienoacene–tetrathiafulvalene redox systems

@en

P2093

Anders Kadziola

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

Cecilie Lindholm Andersen

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

Christian R. Parker

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

Gabriel E. Rudebusch

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

Michael M. Haley

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

Mikkel A. Christensen

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

Mogens Brøndsted Nielsen

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

Ole Hammerich

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

P2860

Salts of extended tetrathiafulvalene analogues: relationships between molecular structure, electrochemical properties and solid state organisation

Stable pi-dimer of a tetrathiafulvalene cation radical encapsulated in the cavity of cucurbit[8]uril.

Effects of structural factors on the pi-dimerization and/or disproportionation of the cation radical of extended TTF containing thiophene-based pi-conjugated spacers.

Keys for the existence of stable dimers of bis-tetrathiafulvalene (bis-TTF)-functionalized molecular clips presenting [TTF](•+)···[TTF](•+) long, multicenter bonds at room temperature.

Direct observation of mixed-valence and radical cation dimer states of tetrathiafulvalene in solution at room temperature: association and dissociation of molecular clip dimers under oxidative control.

Tetrathiafulvalene radical cation dimerization in a bistable tripodal [4]rotaxane.

Molecular and electronic structures of the long-bonded pi-dimers of tetrathiafulvalene cation-radical in intermolecular electron transfer and in (solid-state) conductivity.

Mixed valence radical cations and intermolecular complexes derived from indenofluorene-extended tetrathiafulvalenes

Tetrathiafulvalene-functionalized triptycenes: synthetic protocols and elucidation of intramolecular Coulomb repulsions in the oxidized species

P304

49748-49751

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

P31

scholarly article

P356

10.1039/C5RA09581F

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

P433

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

P478

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

P577

2015-01-01T00:00:00Z

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Diindenothienoacene–tetrathiafulvalene redox systems

about

P2860

P2860

Diindenothienoacene–tetrathiafulvalene redox systems

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577