Аннотация:
A prototropic rearrangement of a number of hydrophosphorylic compounds has been found to proceed by a bimolecular mechanism with tunneling predominant at temperatures below 340 K.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
V. M. Mamaev, A. V. Prisyajnuk, D. N. Laikov, L. S. Logutenko, Yu. V. Babin, “The mechanism of a diad prototropic rearrangement of hydrophosphorylic compounds”, Mendeleev Commun., 9:6 (1999), 240–241
Ashim Nandi, Jan M. L. Martin, “Thermally‐Activated Tunneling in the Two‐Water Bridge Catalyzed Tautomerization of Phosphinylidene Compounds**”, ChemPhysChem, 23:22 (2022)
Daniella Vincze, Péter Ábrányi-Balogh, Péter Bagi, György Keglevich, “A Mechanistic Study on the Tautomerism of H-Phosphonates, H-Phosphinates and Secondary Phosphine Oxides”, Molecules, 24:21 (2019), 3859
Guilhem Javierre, Rémy Fortrie, Marion Jean, Delphine Moraleda, Jean-Valère Naubron, Frédéric Fotiadu, “Racemization and transesterification of alkyl hydrogeno-phenylphosphinates”, J Mol Model, 23:5 (2017)
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Benjamin G. Janesko, Henry C. Fisher, Mark J. Bridle, Jean-Luc Montchamp, “P(═O)H to P–OH Tautomerism: A Theoretical and Experimental Study”, J. Org. Chem., 80:20 (2015), 10025
Yu. A. Ustynyuk, Yu. V. Babin, “Tautomerism of hydrophosphoryl compounds and their features as ligands in metal complex catalysis. Quantum-chemical simulations by the density functional method”, Russ J Gen Chem, 78:4 (2008), 822
A. V. Prisyajnuk, Yu. V. Babin, “Theoretical study of diad prototropic rearrangement in fluorinated methylphosphonic acid N,N-dimethylamides”, Mendeleev Commun., 12:4 (2002), 153–153
V. M. Mamaev, A. V. Prisyajnuk, L. S. Logutenko, Yu. V. Babin, “Prototropic rearrangement in fluorine-substituted hypophosphoric acid dimethylamides”, Mendeleev Commun., 11:6 (2001), 221–222
V. M. Mamaev, A. V. Prisyajnuk, L. S. Logutenko, Yu. V. Babin, “A theoretical study of the tautomeric forms of hydrophosphorilic compounds”, Mendeleev Commun., 10:6 (2000), 230–231