The first examples of a pi-conjugated benzo[b]phosphole P-oxide in which two phosphole P-oxide units are connected by a carbon-carbon double bond are described. The molecules are synthesized as E isomers with respect to the carbon-carbon double bond and exist as stable cis and trans isomers (chiral and meso one respectively) relatively to the two stereogenic P atoms. The optical and electrochemical properties of both isomers have been investigated by experiment and computations.
Highly Conjugated Bis(benzo[b]phosphole)‐P‐oxides: Synthesis and Electrochemical, Optical, and Computational Studies / N. D'Imperio, V. Pelliccioli, S. Grecchi, A. Bossi, F. Vasile, S. Cauteruccio, A.I. Arkhypchuk, A. Kumar Gupta, A. Orthaber, S. Ott, E. Licandro. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1434-193X. - 26:4(2023 Jan 24), pp. e202201209.1-e202201209.10. [10.1002/ejoc.202201209]
Highly Conjugated Bis(benzo[b]phosphole)‐P‐oxides: Synthesis and Electrochemical, Optical, and Computational Studies
V. PelliccioliSecondo
;S. Grecchi;F. Vasile;S. Cauteruccio;E. Licandro
Ultimo
2023
Abstract
The first examples of a pi-conjugated benzo[b]phosphole P-oxide in which two phosphole P-oxide units are connected by a carbon-carbon double bond are described. The molecules are synthesized as E isomers with respect to the carbon-carbon double bond and exist as stable cis and trans isomers (chiral and meso one respectively) relatively to the two stereogenic P atoms. The optical and electrochemical properties of both isomers have been investigated by experiment and computations.File | Dimensione | Formato | |
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