Chiroptical and Redox Properties of a Tetrathiafulvalene Analogue with an Inserted Spiro Framework
Author:
Affiliation:
1. School of Science, Kitasato University, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0373, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.180358
Reference32 articles.
1. Chiroptical Molecular Switches
2. Redox-triggered chiroptical molecular switches
3. Macrocyclic Oligothiophene with Stereogenic [2.2]Paracyclophane Scaffolds: Chiroptical Properties from π-Transannular Interactions
4. Synthesis, Optical Resolution, and Circularly Polarized Luminescence of an Axially Chiral Porphyrin Dimer
5. Concentration-dependent circularly polarized luminescence (CPL) of chiral N,N′-dipyrenyldiamines: sign-inverted CPL switching between monomer and excimer regions under retention of the monomer emission for photoluminescence
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2. Stereogenic π-Conjugated Macrocycles: Synthesis, Structure, and Chiroptical Properties Including Circularly Polarized Luminescence;Synlett;2023-08-22
3. Progressive framework designing and photocurrent responsive tuning based on tetra(4-pyridyl)-tetrathiafulvalene ligand;Journal of Solid State Chemistry;2022-12
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