Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Self-assembly of hydrogen-bonded cage tetramers of phosphonic acid. / Giba, Ivan S.; Tolstoy, Peter M.
в: Symmetry, Том 13, № 2, 258, 04.02.2021, стр. 1-12.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - Self-assembly of hydrogen-bonded cage tetramers of phosphonic acid
AU - Giba, Ivan S.
AU - Tolstoy, Peter M.
N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/2/4
Y1 - 2021/2/4
N2 - The self-association of phosphonic acids with general formula RP(O)(OH)2 in solution state remains largely unexplored. The general understanding is that such molecules form multiple intermolecular hydrogen bonds, but the stoichiometry of self-associates and the bonding motifs are unclear. In this work, we report the results of the study of self-association of tert-butylphosphonic acid using low temperature liquid-state1H and31P NMR spectroscopy (100 K; CDF3/CDF2Cl) and density functional theory (DFT) calculations. For the first time, we demonstrate conclusively that polar aprotic medium tert-butylphosphonic acid forms highly symmetric cage-like tetramers held by eight OHO hydrogen bonds, which makes the complex quite stable. In these associates. each phosphonic acid molecule is bonded to three other molecules by forming two hydrogen bonds as proton donor and two hydrogen bonds as proton acceptor. Though the structure of such cage-like tetramers is close to tetrahedral, the formal symmetry of the self-associate is C2 .
AB - The self-association of phosphonic acids with general formula RP(O)(OH)2 in solution state remains largely unexplored. The general understanding is that such molecules form multiple intermolecular hydrogen bonds, but the stoichiometry of self-associates and the bonding motifs are unclear. In this work, we report the results of the study of self-association of tert-butylphosphonic acid using low temperature liquid-state1H and31P NMR spectroscopy (100 K; CDF3/CDF2Cl) and density functional theory (DFT) calculations. For the first time, we demonstrate conclusively that polar aprotic medium tert-butylphosphonic acid forms highly symmetric cage-like tetramers held by eight OHO hydrogen bonds, which makes the complex quite stable. In these associates. each phosphonic acid molecule is bonded to three other molecules by forming two hydrogen bonds as proton donor and two hydrogen bonds as proton acceptor. Though the structure of such cage-like tetramers is close to tetrahedral, the formal symmetry of the self-associate is C2 .
KW - Hydrogen bond
KW - Low-temperature NMR
KW - Phosphonic acid
KW - Self-association
KW - Tetramer
KW - self-association
KW - phosphonic acid
KW - tetramer
KW - hydrogen bond
KW - low-temperature NMR
UR - http://www.scopus.com/inward/record.url?scp=85100520964&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/7dcecd5b-b2ee-3b9a-8c09-dab6863482c9/
U2 - 10.3390/sym13020258
DO - 10.3390/sym13020258
M3 - Article
AN - SCOPUS:85100520964
VL - 13
SP - 1
EP - 12
JO - Symmetry
JF - Symmetry
SN - 2073-8994
IS - 2
M1 - 258
ER -
ID: 85605076