Phosphine telluride
A phosphine telluride refers to organophosphorus compounds with the formula R3PTe (R = alkyl or aryl). They are structurally analogous to phosphine oxides, phosphine sulfides, and phosphine selenides. Unlike other members of this series, the phosphine tellurides are labile with respect to loss of the chalcogen. Aryl-substituted phosphine telluridew tend to lose tellurium easier. Nonetheless, several members have been characterized by X-ray crystallography, which reveals a tetrahedral phosphorus center with a P-Te bond length of 236 picometers.[1] [2] Simple trialkylphosphine tellurides are pale yellow solids.[3]
Phosphine tellurides like trioctylphoshine telluride, tributylphosphine telluride and tricyclohexylphosphine telluride are reagents used in the preparation of metal telluride nanoparticles.[4] [5]
References[edit]
- ^ Jeremias, Lukáš; Babiak, Michal; Kubát, Václav; Calhorda, Maria José; Trávníček, Zdeněk; Novosad, Josef (2014). "Successful Oxidation of Ph2P(CH2)nPPh2 (n = 2, 4, 6) by Tellurium Leading to Ph2P(Te)(CH2)nP(Te)Ph2". RSC Advances. 4 (30): 15428. Bibcode:2014RSCAd...415428J. doi:10.1039/C4RA00157E.
- ^ Jones, C. H. W.; Sharma, R. D. (1987). "Tellurium-125 NMR and Moessbauer Spectroscopy of Tellurium-Phosphine Complexes and the Tellurocyanates". Organometallics. 6 (7): 1419–1423. doi:10.1021/om00150a009.
- ^ Zingaro, Ralf; Steeves, Brian H.; Irgolic, Kurt (1965). "Phosphine tellurides". Journal of Organometallic Chemistry: 320-323. doi:10.1016/s0022-328x(00)88840-3.
- ^ García-Rodríguez, Raúl; Hendricks, Mark P.; Cossairt, Brandi M.; Liu, Haitao; Owen, Jonathan S. (2013). "Conversion Reactions of Cadmium Chalcogenide Nanocrystal Precursors". Chemistry of Materials. 25 (8): 1233–1249. doi:10.1021/cm3035642.
- ^ Shuklov, I.A.; Mardini, A.A.; Skabitsky, I.V.; Dubrovina, N.V.; Lizunova, A.; Razumov, V. "Rational development of new phosphine telluride precursors for the synthesis of telluride quantum dots". Nano-Structures & Nano-Objects. 35: 101020. doi:10.1016/j.nanoso.2023.101020.