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Atomic Level Mechanism of the White Phosphorous Demolition by Di-iodine

preprint
submitted on 08.11.2017 and posted on 09.11.2017 by Carlo Mealli, Andrea Ienco, Maurizio Peruzzini, Gabriele Manca
A detailed mechanism of the I2-induced transformation of white phosphorus into PI3 emerges from a DFT analysis. The multi-step process implies at any stage one P P and two I I bond cleavages, associated to the formation of two P I bonds plus an in situ generated brand new I2 molecule. Significant electron transfer between atoms is observed at any step, but the reactions better define as concerted rather than redox. Along the steepest descent to the product, no significant barrier is encountered except for the very first P4 activation, which costs +14.6 kcal mol-1. At the atomic level, one first I2 molecule, a typical mild oxidant, is first involved in a linear halogen bonding interaction (XB) with one P donor, while its terminal I atom is engaged in an additional XB adduct with a second I2. Significant electron transfer through the combined diatomics allows the external I atom of the dangling I3 grouping to convey electrons into the * level of one P P bond with its consequent cleavage. This implies at some point the appearance of a six-membered ring, which alternative switches its bonding and no-bonding interactions. The final transformation of the P2I4 diphosphine into two PI3 phosphines is enlightening also for the specific role of the I substituents. In fact, it is proved that an organo-diphosphine analogue hardly undergoes the separation of two phosphines, as reported in literature. This is attributable to the particularly high donor power of the carbo-substituted P atoms, which prevents the concertedness of the reaction but favors charge separation in an unreactive ion pair.

Funding

European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (Grant Agreement No. 670173) for funding the project PHOSFUN “Phosphorene functionalization: a new platform for advanced multifunctional materials

History

Topic

  • Main Group Chemistry (Inorg.)
  • Bonding
  • Reaction (Inorg.)
  • Small Molecule Activation (Inorg.)

Email Address of Submitting Author

andrea.ienco@cnr.it

Email Address(es) for Other Author(s)

gabriele.manca@cnr.it maurizio.peruzzini@cnr.it carlo.mealli@iccom.cnr.it

Institution

CNR-ICCOM Via Madonna del Piano 10, Sesto Fiorentino, Firenze

Country

Italy

ORCID For Submitting Author

0000-0002-2586-4943

Declaration of Conflict of Interest

No conflict of interest

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