Electronic structure of zwitterionic diamino-meta-quinonoid molecules: identity of UV absorption bands
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Reference17 articles.
1. Double Stereodifferentiation in Carbohydrate Coupling Reactions: The Mismatched Interaction of Donor and Acceptor as an Unprecedented Factor Governing theα/β Ratio of Glycoside Formation
2. Incorporation of hydration effects within the semiempirical molecular orbital framework. AM1 and MNDO results for neutral molecules, cations, anions, and reacting systems
3. Unprecedented zwitterion in quinonoid chemistryElectronic supplementary information (ESI) available: spectroscopic data for 4 and 6 and an ORTEP view of the structure of 4. See http://www.rsc.org/suppdata/cc/b1/b107828n/.
4. A 6π + 6π Potentially Antiaromatic Zwitterion Preferred to a Quinoidal Structure: Its Reactivity Toward Organic and Inorganic Reagents
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1. Regioselective addition of DDQ on a quinoid ring: an entry into chiral zwitterionic bridging ligands;New Journal of Chemistry;2018
2. Methanol-Triggered Vapochromism Coupled with Solid-State Spin Switching in a Nickel(II)-Quinonoid Complex;Angewandte Chemie International Edition;2017-01-23
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