Synthesis of 1,4-Benzoquinone Derivatives Having Two Side-Armed Polyethers and Crown Ethers, and Their Electrochemical Study in the Presence of Alkali Metal Cations (Na+and K+)
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/61/8/61_8_3026/_pdf
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1. Redox-switched crown ethers. 3. Cyclic-acyclic interconversion coupled with redox between dithiol and disulfide and its application to membrane transport
2. Redox-active crown ethers: molecules designed to couple ion binding with a redox reaction
3. One-step synthesis and electrochemically enhanced cation-binding properties of novel “quinonoid crown ethers”
4. Electrochemical switching in anthraquinone-substituted carbon-pivot lariat ethers and podands: chain length effects in geometric and electronic cooperativity
5. Synthetic macrocyclic ligands. III. Synthesis of a quinone-hydroquinone redox system incorporated with complexing ability toward cations
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1. Quinones based molecular receptors for recognition of anions and metal ions;Tetrahedron;2014-07
2. The chemistry of constrained crown ring systems and fluorescence sensor applications;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2012-08-07
3. Electrochemical and spectroscopic studies on redox-switching behavior of quinone-derivatized supramolecules;Current Applied Physics;2009-07
4. Self-Activated Supramolecular Reactions: Effects of Host−Guest Recognition on the Kinetics of the Diels−Alder Reaction of Open-Chain Oligoether Quinones with Cyclopentadiene;Journal of the American Chemical Society;2003-04-19
5. Effects of Host−Guest Recognition on Kinetics of Diels−Alder Reaction of Quinocrown Ethers with Cyclopentadiene;The Journal of Organic Chemistry;2002-01-25
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