Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Protonation of ninhydrin and indan-1,2,3-trione revisited : A combined theoretical and experimental study. / Salnikov, George E.; Genaev, Alexander M.; Shernyukov, Andrey V. и др.
в: Journal of Molecular Structure, Том 1134, 15.04.2017, стр. 1-5.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - Protonation of ninhydrin and indan-1,2,3-trione revisited
T2 - A combined theoretical and experimental study
AU - Salnikov, George E.
AU - Genaev, Alexander M.
AU - Shernyukov, Andrey V.
AU - Shubin, Vyacheslav G.
PY - 2017/4/15
Y1 - 2017/4/15
N2 - The literature data on protonation of indan-1,2,3-trione and ninhydrin (indantrione hydrate) in acidic media are inconsistent, formation of dications at pH 3 and very low extent of protonation in superacid CF3SO3H were claimed. Our combined theoretical (DFT, MP2, CCSD) and experimental (NMR) study has shown that indantrione undergoes single protonation in CF3SO3H resulting in monocation formation. In more strong superacid FSO3H-SbF5 dication is formed, but, contrary to the literary data, trication is not formed even in this superacid. Significant dependence of 13C NMR chemical shifts of indantrione on media acidity allows using this compound as a convenient indicator of acidity in a broad range, from H0 −3 to −25.
AB - The literature data on protonation of indan-1,2,3-trione and ninhydrin (indantrione hydrate) in acidic media are inconsistent, formation of dications at pH 3 and very low extent of protonation in superacid CF3SO3H were claimed. Our combined theoretical (DFT, MP2, CCSD) and experimental (NMR) study has shown that indantrione undergoes single protonation in CF3SO3H resulting in monocation formation. In more strong superacid FSO3H-SbF5 dication is formed, but, contrary to the literary data, trication is not formed even in this superacid. Significant dependence of 13C NMR chemical shifts of indantrione on media acidity allows using this compound as a convenient indicator of acidity in a broad range, from H0 −3 to −25.
KW - Ninhydrin
KW - NMR
KW - Quantum chemistry calculations
KW - Superacid
KW - AROMATIC-COMPOUNDS
UR - http://www.scopus.com/inward/record.url?scp=85007328532&partnerID=8YFLogxK
U2 - 10.1016/j.molstruc.2016.12.057
DO - 10.1016/j.molstruc.2016.12.057
M3 - Article
AN - SCOPUS:85007328532
VL - 1134
SP - 1
EP - 5
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
SN - 0022-2860
ER -
ID: 10040811