Synthesis, Properties, and Redox Behaviors of Di- and Trications Composed of Di(1-azulenyl)methylium Units Connected byp- andm-Phenylene and 1,3,5-Benzenetriyl Spacers
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/73/8/73_8_1865/_pdf
Reference24 articles.
1. Azulene analogues of triphenylmethyl cation; extremely stable hydrocarbon carbocations
2. Tris(3,6-di-t-butyl-1-azulenyl)methyl cation; hydrocarbon cation with the highest pKR+ value
3. Dynamic stereochemistry of tri(2-methyl-1-azulenyl)methyl cation; steric effect of 2-methyl groups on rotational barriers and mechanism
4. Syntheses of Azulene Analogues of Triphenylmethyl Cation: Extremely Stable Hydrocarbon Carbocations and the First Example of a One-Ring Flip as the Threshold Rotation Mechanism for Molecular Propellers
5. Synthesis and Dynamic Stereochemistry of a Tri(1-azulenyl)methyl Cation Containing a Different Substituent on Each Azulene Ring
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1. Bis(3-methylthio-1-azulenyl)phenylmethyl Cations and Dications Connected by a 1,4-Phenylene Spacer: Synthesis and Their Electrochemical Properties;Organics;2022-12-16
2. Diazulenylmethyl Cations with a Silicon Bridge: A π-Extended Cationic Motif to Form J-Aggregates with Near-Infrared Absorption and Emission;Journal of the American Chemical Society;2022-10-28
3. Azulene Moiety as Electron Reservoir in Positively Charged Systems; A Short Survey;Symmetry;2021-03-24
4. Cyanine–cyanine hybrid structure as a stabilized polyelectrochromic system: synthesis, stabilities, and redox behavior of di(1-azulenyl)methylium units connected with electron-accepting π-electron systems;Arkivoc;2017-11-26
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