1. Monireh Zarghani, Batool Akhlaghinia, “Green and Efficient Procedure for Suzuki–Miyaura and Mizoroki–Heck Coupling Reactions Using Palladium Catalyst Supported on Phosphine Functionalized ZrO2 NPs (ZrO2@ECP-Pd) as a New Reusable Nanocatalyst”, Bulletin of the Chemical Society of Japan, 89:10 (2016), 1192  crossref
  2. A. M. Safiulina, A. G. Matveeva, D. V. Ivanets, E. M. Kudryavtsev, M. S. Grigor´ev, V. E. Baulin, A. Yu. Tsivadze, “Phosphoryl-containing acidic podands as extractants for recovery of f-elements”, Russ Chem Bull, 64:1 (2015), 161  crossref
  3. Ali Khalafi-Nezhad, Farhad Panahi, “Phosphine-functionalized magnetic nanoparticles (PFMN) as a magnetic recyclable phosphorus ligand: Preparation of its palladium(II) complex for Heck reaction of chloroarenes”, Journal of Organometallic Chemistry, 741-742 (2013), 7  crossref
  4. Ilya G. Shenderovich, “Effect of Noncovalent Interactions on the 31P Chemical Shift Tensor of Phosphine Oxides, Phosphinic, Phosphonic, and Phosphoric Acids, and Their Complexes with Lead(II)”, J. Phys. Chem. C, 117:50 (2013), 26689  crossref
  5. Olivier P. J. Vieuxmaire, Rémi E. Piau, Fabienne Alary, Jean-Louis Heully, Pierre Sutra, Alain Igau, Martial Boggio-Pasqua, “Theoretical Investigation of Phosphinidene Oxide Polypyridine Ruthenium(II) Complexes: Toward the Design of a New Class of Photochromic Compounds”, J. Phys. Chem. A, 117:48 (2013), 12821  crossref
  6. Natalie E. Mansfield, Martyn P. Coles, Peter B. Hitchcock, “Examining the stability of phospha(III)guanidines: Formation of a formamidinium:phosphinate ion-pair and an N-protonated phospha(III)guanidinium chloride”, Polyhedron, 37:1 (2012), 9  crossref
  7. I. V. Ananyev, P. Yu. Barzilovich, K. A. Lyssenko, “Evidence for the Zundel-like Character of Oxoethylidenediphosphonic Acid Hydrate”, Mendeleev Commun., 22:5 (2012), 242–244  mathnet  crossref
  8. Adrian Mermer, Przemysław Starynowicz, “Charge-density distribution in hydrogen methylphosphonates of calcium and lithium”, Acta Crystallogr B Struct Sci, 67:5 (2011), 399  crossref
  9. Ivan S. Bushmarinov, Orudzh G. Nabiev, Remir G. Kostyanovsky, Mikhail Yu. Antipin, Konstantin A. Lyssenko, “The azide anion as a building block in crystal engineering from a charge density point of view”, CrystEngComm, 13:8 (2011), 2930  crossref
  10. Andrew R. Shaffer, Nihal Deligonul, Daniel A. Scherson, John D. Protasiewicz, “A Hybrid Lithium Oxalate-Phosphinate Salt”, Inorg. Chem., 49:23 (2010), 10756  crossref
  11. Yu. V. Nelyubina, G. A. Gazieva, V. V. Baranov, P. A. Belyakov, A. O. Chizhov, K. A. Lyssenko, A. N. Kravchenko, “The synthesis, structure, and electron density distribution in crystals of 4,5-dihydroxyimidazolidine-2-thiones”, Russ Chem Bull, 58:7 (2009), 1353  crossref
  12. K. A. Lyssenko, P. Yu. Barzilovich, Yu. V. Nelyubina, E. A. Astaf'ev, M. Yu. Antipin, S. M. Aldoshin, “Charge transfer and hydrogen bond energy in glycinium salts”, Russ Chem Bull, 58:1 (2009), 31  crossref
  13. Yulia V. Nelyubina, Sergey I. Troyanov, Mikhail Yu. Antipin, Konstantin A. Lyssenko, “Why Oxonium Cation in the Crystal Phase is a Bad Acceptor of Hydrogen Bonds: A Charge Density Analysis of Potassium Oxonium Bis(hydrogensulfate)”, J. Phys. Chem. A, 113:17 (2009), 5151  crossref
  14. Ivan S. Bushmarinov, Mikhail Yu. Antipin, Vnira R. Akhmetova, Guzel R. Nadyrgulova, Konstantin A. Lyssenko, “Stereoelectronic Effects in N-C-S and N-N-C Systems: Experimental andab InitioAIM Study”, J. Phys. Chem. A, 112:22 (2008), 5017  crossref
  15. Lada N. Puntus, Konstantin A. Lyssenko, Mikhail Yu. Antipin, Jean-Claude G. Bünzli, “Role of Inner- and Outer-Sphere Bonding in the Sensitization of EuIII-Luminescence Deciphered by Combined Analysis of Experimental Electron Density Distribution Function and Photophysical Data”, Inorg. Chem., 47:23 (2008), 11095  crossref
  16. Sergey S. Bukalov, Larissa A. Leites, Konstantin A. Lyssenko, Rinat R. Aysin, Alexander A. Korlyukov, Jan V. Zubavichus, Konstantin Yu. Chernichenko, Elizabeth S. Balenkova, Valentine G. Nenajdenko, Mikhail Yu. Antipin, “Two Modifications Formed by “Sulflower” C16S8Molecules, Their Study by XRD and Optical Spectroscopy (Raman, IR, UV-Vis) Methods”, J. Phys. Chem. A, 112:43 (2008), 10949  crossref
  17. Alexandra O. Borissova, Alexander A. Korlyukov, Mikhail Yu. Antipin, Konstantin A. Lyssenko, “Estimation of Dissociation Energy in Donor-Acceptor Complex AuCl·PPh3via Topological Analysis of the Experimental Electron Density Distribution Function”, J. Phys. Chem. A, 112:46 (2008), 11519  crossref
  18. Yu. V. Nelyubina, K. A. Lyssenko, R. G. Kostyanovsky, D. A. Bakulin, M. Yu. Antipin, “ClO3–···ClO3 – interactions in crystalline sodium chlorate”, Mendeleev Commun., 18:1 (2008), 29–31  mathnet  crossref
  19. Konstantin A. Lyssenko, Alexander A. Korlyukov, Denis G. Golovanov, Sergey Yu. Ketkov, Mikhail Yu. Antipin, “Estimation of the Barrier to Rotation of Benzene in the (η6-C6H6)2Cr Crystal via Topological Analysis of the Electron Density Distribution Function”, J. Phys. Chem. A, 110:20 (2006), 6545  crossref
  20. R.E. Asfin, G.S. Denisov, K.G. Tokhadze, “The ν(OH/OD) band shape of strong hydrogen bonded dimers of phosphinic acids. Phenomenology and formation models”, Journal of Molecular Structure, 790:1-3 (2006), 11  crossref
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