A.I. Kuramshin*, E.V. Kolpakova**, R.A. Cherkasov***, V.I. Galkin****

Kazan Federal University, Kazan, 420008 Russia

E-mail: *fea_naro@mail.ru, **argironet@gmail.com, ***Rafael.Cherkasov@kpfu.ru, ****Vladimir.Galkin@kpfu.ru

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Abstract

Using quantum-chemical calculations carried out for interpretation of the experimentally discovered reactivity of 1-hetero-1,3-dienes that are mono- and bidentally coordinated with the transition metal core, we have revealed that the difference in hydrophosphorylation directions of the free organic molecule and the same molecule involved in the coordination sphere of the transition metal can be explained by either weakening or complete loss of conjugation between the C=C and C=X fragments as a result of coordination.

In the case of monodentate coordination of heterodiene with the transition metal according to the η2(C,C)-type, the conjugation weakening is suggested to be maximum for the transition metal characterized by the minimum electronegativity, which predetermines the increased contribution of the metalcyclopropane resonance structure into the general bonding mode. Organometallic compounds having the heterodiene ligand bidentally coordinated demonstrate the conjugation weakening parallel to the metal radius.

Keywords: quantum-chemical calculations, metal-organic derivatives of chromium group metals, density functional (DFT), conjugation, stress energy

Figure captions

Fig. 1. Dependence of the energy of heterodiene ligand stress via the metal core on the electronegativity of the metal.

Fig. 2. Dependence of the energy of heterodiene ligand stress via the metal core on the valent radius of the metal.

References

  1. Galkin V.I., Galkina I.V., Courdi Kh.A., Denisov B.V., Cherkasov R.A. The reactions of dialkylphosphites with α-enones coordinated in p-complexes of iron carbonyls. Metallorg. Khim., 1990, vol. 3, no. 6, pp. 1429–1431. (In Russian)
  2. Kuramshin A.I., Karpenko E.A., Cherkasov R.A. Synthesis and hydrophosphorylation of adducts of 1,3-diphenylprop-2-en-1-one and 4-phenylbut-3-en-2-one with carbonyl complexes of group VIB metals. Russ. J. Gen. Chem., 1999, vol. 69, no. 7, pp. 1176–1177.
  3. Kuramshin A.I., Karpenko E.A., Cherkasov R.A. Hydrophosphorylation of 1,3-diphenyl-2-propen-1-one and 4-phenyl-3-buten-2-one in the coordinational sphere of carbonyl complexes of group VIB metals. Russ. J. Gen. Chem., 2001, vol. 71, no. 2, pp. 191–195.
  4. Kuramshin A.I., Kuramshina E.A., Cherkasov R.A. Synthesis of mesityl oxide π-complexes with metals of chromium subgroup and with iron. Theoretical and experimental investigation of the ligand dissociation energy. Russ. J. Org. Chem., 2005, vol. 41, no. 5, pp. 649–655.
  5. Kuramshin A.I., Kuramshina E.A., Cherkasov R.A. Synthesis, structure, and hydrophosphorylation of π-complexes derived from tert-butyl(1,3-dimethyl-2-butenylidene)amine and homoligand iron(0) and group VIb metal carbonyls. Russ. J. Org. Chem., 2005, vol. 40, no. 9, pp. 1265–1273.
  6. Kuramshin A.I., Pavlova I.V., Cherkasov R.A. Synthesis and structure of cyclopropenone π-complexes with pentacarbonyliron(0) and hexacarbonyltungsten(0). Hydrophosphorylation of cyclopropenone in the transition metal coordination sphere. Russ. J. Org. Chem., 2004, vol. 40, no. 1, pp. 45–49.
  7. Kuramshin A.I., Asafyeva E.V., Cherkasov R.A. Preparation of complexes η4-4-(1,3-diphenyl-2-propen-1-one)-η3-3-(1,3,5-triorganyl-1,3,5-triazacyclohexane)carbonyltungsten(0) and their reactions with diethyl phosphite. Russ. J. Org. Chem., 2005, vol. 41, no. 5, pp. 779–783.
  8. Kuramshin A.I., Kolpakova E.V., Kuramshina E.A., Galkin V.I. Cherkasov R.A. The synthesis of p,n-complexes of 1-thio-1,3-dienes with chromium group metals. The inner-sphere hydrophosphorylation of α-enethiones. Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki, 2015, vol. 157, no. 2, pp. 143–161. (In Russian)
  9. Kuramshin A.I., Vatsadze S.Z., Galkin V.I., Cherkasov R.A. Synthesis and hydrophosphorylation of π-complexes of dibenzylideneacetone and cyclic conjugated dienones with homocarbonyl and carbonylcyclopentadienyl molybdenum compounds. Russ. J. Gen. Chem., 2016, vol. 86, no. 3, pp. 645–655.
  10. Jones R.O., Gunnarsson O. The density functional formalism, its applications and prospects. Rev. Mod. Phys., 1989, vol. 61, no. 3, pp. 689–746.
  11. Kuramshin A.I., Zimaliev M.V., Kolpakova E.V., Galkin V.I. The selection of appropriate quantum-chemical model for calculations of properties of chromium group complexes via DFT. Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki, 2016, vol. 158, no. 1, pp. 34–43. (In Russian)
  12. Pearson R.G. Absolute electronegativity and absolute hardness of lewis acids and bases. J. Am. Chem. Soc., 1985, vol. 107, no. 24, pp. 6801–6806.
  13. Frenking G. Understanding the nature of the bonding in transition metal complexes: from Dewar's molecular orbital model to an energy partitioning analysis of the metal-ligand bond. J. Organomet. Chem., 2001, vol. 635, no. 1, pp. 9–23.
  14. Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Zakrzewski V.G., Montgomery J.A., Stratmann R.E., Burant J.C., Dapprich S., Millam J.M., Daniels A.D., Kudin K.N., Strain M.C., Farkas O., Tomasi J., Barone V., Cossi M., Cammi R., Mennucci B., Pomelli C., Adamo C., Clifford S., Ochterski J., Petersson G.A., Ayala P.Y., Cui Q., Morokuma K., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Cioslowski J., Ortiz J.V., Baboul A.G., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Gomperts R., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Andres J.L., Gonzalez C., Head-Gordon M., Replogle E.S., Pople J.A. Gaussian 98, Revision A.9. Pittsburgh, PA, Gaussian Inc., 1998.

For citation: Kuramshin A.I., Kolpakova E.V., Cherkasov R.A., Galkin V.I. The conjugation stress of ligand via metal core as the cause of changes in the reactivity of coordinated 1-hetero-1,3-dienes. Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki, 2016, vol. 158, no. 2, pp. 176–186. (In Russian)


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