Reversible Photoisomerization of Monolayers of π‐Expanded Oligothiophene Macrocycles at Solid–Liquid Interfaces
Author:
Affiliation:
1. Department of Physics & IRIS Adlershof Humboldt-Universität zu Berlin Newtonstr. 15 12489 Berlin Germany
2. Department of Chemistry Graduate School of Science and Engineering Tokyo Metropolitan University Hachioji Tokyo 192-0397 Japan
Funder
Deutsche Forschungsgemeinschaft
Strategic International Collaborative Research Program
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201809514
Reference41 articles.
1. Molecular Electronics. Synthesis and Testing of Components
2. Structural order in conjugated oligothiophenes and its implications on opto-electronic devices
3. Functional oligothiophenes as advanced molecular electronic materials
4. Synthesis of the First Fullyα-Conjugated Macrocyclic Oligothiophenes: Cyclo[n]thiophenes with Tunable Cavities in the Nanometer Regime
5. Synthese der ersten vollständigα-konjugierten makrocyclischen Oligothiophene: Cyclo[n]thiophene mit einstellbaren Hohlräumen im Nanometerregime
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1. A Macrocyclic Furan with Accessible Oxidation States: Switching Between Aromatic and Antiaromatic Global Ring Currents;Chemistry – A European Journal;2022-09-02
2. Ring Size Determines the Conformation, Global Aromaticity and Photophysical Properties of Macrocyclic Oligofurans;Chemistry – A European Journal;2021-11-29
3. π‐Conjugated Macrocycles Bearing Angle‐Strained Alkynes;Chemistry – A European Journal;2019-12-16
4. A macrocyclic oligofuran: synthesis, solid state structure and electronic properties;Chemical Science;2019
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