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Anthryl-Substituted 3‑Silylene-2-silaaziridine Obtained by Isomerization of Disilacyclopropanimine: An Exocyclic Silene Showing a Distinct Intramolecular Charge Transfer Transition
Abstract
An anthryl-substituted exocyclic silene, 3-silylene-2-silaaziridine, was synthesized by isomerization of the corresponding disilacyclopropanimine. The UV–vis spectrum of the silene shows a distinct intramolecular charge transfer (ICT) transition from the π orbital of the SiC double bond to the π* orbital of the anthryl moiety. The relatively high-lying π(SiC) orbital of the 3-silylene-2-silaaziridine moiety and the low-lying π* orbital of the anthryl group would be responsible for the distinct ICT band- Text
- Journal contribution
- Medicine
- Cell Biology
- Physiology
- Immunology
- Chemical Sciences not elsewhere classified
- Physical Sciences not elsewhere classified
- UV
- Distinct
- Transfer
- silylene
- spectrum
- Disilacyclopropanimine
- Charge
- anthryl moiety
- anthryl group
- TransitionAn
- exocyclic
- disilacyclopropanimine
- ICT band
- silene
- intramolecular charge transfer
- Obtained
- Exocyclic Silene
- Isomerization
- transition
- Silylene
- Intramolecular
- isomerization
- bond