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'''Diphosphorus''', P<sub>2</sub>, is the ] form of ].<ref>Russell, C. A. (2010), PP, a Laboratory Reagent?. Angewandte Chemie International Edition, 49: 9572–9573. {{doi|10.1002/anie.201006243}}</ref> Unlike its ] neighbor ] which forms a stable N<sub>2</sub> molecule with a nitrogen to nitrogen ], phosphorus prefers a tetrahedral form P<sub>4</sub> because P-P ]s are high in energy. Diphosphorus is therefore very reactive with a ] (117 ]/] or 490 ]/mol) half that of ]. | '''Diphosphorus''', P<sub>2</sub>, is the ] form of ].<ref>Russell, C. A. (2010), PP, a Laboratory Reagent?. Angewandte Chemie International Edition, 49: 9572–9573. {{doi|10.1002/anie.201006243}}</ref> Unlike its ] neighbor ], which forms a stable N<sub>2</sub> molecule with a nitrogen to nitrogen ], phosphorus prefers a tetrahedral form P<sub>4</sub> because P-P ]s are high in energy. Diphosphorus is, therefore, very reactive with a ] (117 ]/] or 490 ]/mol) half that of ]. | ||
Diphosphorus has been generated by heating ] at 1100 ]s. Nevertheless, some advancements have been obtained in generating the diatomic molecule in homogeneous solution, under normal conditions with the use by some ] ] (based on, for example, ] and ]).<ref>''Triple-Bond Reactivity of Diphosphorus Molecules'' Nicholas A. Piro, Joshua S. Figueroa, Jessica T. McKellar, Christopher C. Cummins ] 1 September '''2006''':Vol. 313. no. 5791, pp. 1276–1279 ]</ref><ref>http://www.sciencemag.org/cgi/reprint/313/5791/1276.pdf</ref> | |||
The molecule attracted attention in 2006 when a new method for its synthesis at milder temperatures emerged.<ref>''Triple-Bond Reactivity of Diphosphorus Molecules'' Nicholas A. Piro, Joshua S. Figueroa, Jessica T. McKellar, Christopher C. Cummins ] 1 September '''2006''':Vol. 313. no. 5791, pp. 1276 - 1279 {{doi|10.1126/science.1129630}} PMID 16946068</ref> | The molecule attracted attention in 2006, when a new method for its synthesis at milder temperatures emerged.<ref>''Triple-Bond Reactivity of Diphosphorus Molecules'' Nicholas A. Piro, Joshua S. Figueroa, Jessica T. McKellar, Christopher C. Cummins ] 1 September '''2006''':Vol. 313. no. 5791, pp. 1276 - 1279 {{doi|10.1126/science.1129630}} PMID 16946068</ref> | ||
This method is a variation on nitrogen expulsion in ]s with formation of a ]. The synthesis of the diphosphorus precursor consists of reacting a terminal ] ] with a chloroiminophosphane: | This method is a variation on nitrogen expulsion in ]s with formation of a ]. The synthesis of the diphosphorus precursor consists of reacting a terminal ] ] with a chloroiminophosphane: | ||
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Heating this compound at 50 °C in ] serving as a ] and as a ] |
Heating this compound at 50 °C in ] serving as a ] and as a ] expulses diphosphorus, which is reactive, as it is forms a double ] and the niobium imido compound: | ||
:] | :] |
Revision as of 03:52, 18 November 2011
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Names | |||
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IUPAC name Diphosphorus | |||
Systematic IUPAC name Diphosphyne | |||
Identifiers | |||
CAS Number | |||
3D model (JSmol) | |||
ChEBI | |||
ChemSpider | |||
Gmelin Reference | 1400241 | ||
PubChem CID | |||
CompTox Dashboard (EPA) | |||
InChI
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SMILES
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Properties | |||
Chemical formula | P2 | ||
Molar mass | 61.947523996 g·mol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Diphosphorus, P2, is the diatomic form of phosphorus. Unlike its nitrogen group neighbor nitrogen, which forms a stable N2 molecule with a nitrogen to nitrogen triple bond, phosphorus prefers a tetrahedral form P4 because P-P pi-bonds are high in energy. Diphosphorus is, therefore, very reactive with a bond dissociation energy (117 kcal/mol or 490 kJ/mol) half that of dinitrogen.
Diphosphorus has been generated by heating white phosphorus at 1100 kelvins. Nevertheless, some advancements have been obtained in generating the diatomic molecule in homogeneous solution, under normal conditions with the use by some transition metal complexes (based on, for example, tungsten and niobium).
The molecule attracted attention in 2006, when a new method for its synthesis at milder temperatures emerged.
This method is a variation on nitrogen expulsion in azides with formation of a nitrene. The synthesis of the diphosphorus precursor consists of reacting a terminal niobium phosphide with a chloroiminophosphane:
Heating this compound at 50 °C in 1,3-cyclohexadiene serving as a solvent and as a trapping reagent expulses diphosphorus, which is reactive, as it is forms a double Diels-Alder adduct and the niobium imido compound:
The same imido compound also forms when the thermolysis is performed in toluene but then the fate of diphosphorus is unknown.
P2 has been suggested to form as an intermediate in the photolysis of P4 and in the presence of 2,3-dimethylbutadiene the diphosphane is again formed To date, no direct evidence of P2 formation via P4 photolysis exists.
References
- "Diphosphorus (CHEBI:33472)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
- Russell, C. A. (2010), PP, a Laboratory Reagent?. Angewandte Chemie International Edition, 49: 9572–9573. doi:10.1002/anie.201006243
- Triple-Bond Reactivity of Diphosphorus Molecules Nicholas A. Piro, Joshua S. Figueroa, Jessica T. McKellar, Christopher C. Cummins Science 1 September 2006:Vol. 313. no. 5791, pp. 1276–1279 10.1126/science.1129630
- http://www.sciencemag.org/cgi/reprint/313/5791/1276.pdf
- Triple-Bond Reactivity of Diphosphorus Molecules Nicholas A. Piro, Joshua S. Figueroa, Jessica T. McKellar, Christopher C. Cummins Science 1 September 2006:Vol. 313. no. 5791, pp. 1276 - 1279 doi:10.1126/science.1129630 PMID 16946068
- Optische und photochemische versuche mit phosphor G. Rathenau Physica Volume 4, Issue 6, June 1937, Pages 503-514 doi:10.1016/S0031-8914(37)80084-1
- Tofan, D. and Cummins, C. C. (2010), Photochemical Incorporation of Diphosphorus Units into Organic Molecules. Angewandte Chemie International Edition, 49: 7516–7518. doi: 10.1002/anie.201004385
External links
- Ron Dagani, "A Mild Route To P2, Chemical & Engineering News September 4, 2006 Link