Reactions of acetonyltriphenyl¬phosphonium and 2-butene-1,4-bis(triphenylphosphonium) chlorides with nitric acid

Authors

  • V.V. Sharutin Author
  • D.P. Shevchenko Author
  • K.R. Khazhieva Author

Abstract

Reactions of acetonyltriphenylphosphonium and 2-butene-1,4-bis(triphenylphosphonium) chlorides with nitric acid synthesized alkyltriphenylphosphonium compounds [Ph3PCH2C(O)Me]NO3 (1) and [Ph3PCH2CH=CHCH2PPh3][NO3]2 ∙ 2H2O (2), respectively. The resulting compounds were character-ized by IR spectroscopy and X-ray diffraction analysis (XRD). According to the X-ray diffraction da-ta, acetonyltriphenylphosphonium nitrate (1) [C21H20NO4P, M = 381.35; monoclinic system, sp. gr. C2/c; cell parameters: a = 14.301(13) Å, b = 12.756(11) Å, c = 21.40(2) Å;  = 90.00, β = 90.66(3),  = 90.00, V = 3904(8) Å3, Z = 8; calc = 1.298 g/cm3;  = 0.167 mm–1; F(000) = 1600.0; collection re-gion at 2q: 5.7–56.96; –16 ≤ h ≤ 19, –17 ≤ k ≤ 17, –28 ≤ l ≤ 28; total reflections 46344; independent reflections 4894 (Rint = 0.0808); GOOF = 1.034; R-factor = 0.0631] and (2-butene-1,4-bis(triphenylphosphonium nitrate hydrate (2) [C40H40N2O8P2, M = 738.68; triclinic system, space group P–1; cell parameters: a = 9.259(7) Å, b = 9.514(6) Å, c = 12.247(9) Å;  = 68.43(4), β = 72.47(5),  = 84.06(3), V = 956.7(12) Å3, Z = 2; calc = 1.282 g/cm3;  = 0.168 mm–1; F(000) = 388.0; collection region for 2q: 5.9– 54.34; –11 ≤ h ≤ 11, –12 ≤ k ≤ 12, –15 ≤ l ≤ 15; total reflections 21543; independent reflections 4219 (Rint = 0.0354); GOOF = 1.029; R-factor = 0.0493] have an ionic structure and consist of organyltriphenylphosphoni-um cations with a slightly distorted tetrahedral coordination of the phosphorus atom (the CPC angles vary between 105.5(3)111.8(2) for 1 and 107.61(11)111.28(11) for 2; the P–C distances are 1.751(6)–1.805(5) Å and 1.792(2)–1.815(2) Å, respectively) and planar trigonal nitrate anions (the sums of the ONO angles equal to 359.5 and 360, respectively). Complete tables of atomic coordi-nates, bond lengths, and bond angles of nitrates 1 and 2 have been deposited in the Cambridge Struc-tural Data Bank (CCDC 2338987 (1), 2335887 (2); deposit@ccdc.cam.ac.uk; http://www.ccdc.cam.ac.uk).

Author Biographies

  • V.V. Sharutin
    доктор химических наук, главный научный сотрудник управления научной и инновационной деятельности
  • D.P. Shevchenko
    аспирант, химический факультет, институт естественных и точных наук
  • K.R. Khazhieva
    бакалавр кафедры теоретической и практической химии, институт естественных и точных наук

Published

2024-12-21