Wydział Chemii

Valeriia V. Mulloyarova

Daria O. Ustimchuk

Aleksander Filarowski

Peter M. Tolstoy

2020

Molecules

25

1907/1-1907/17

10.3390/molecules25081907

Naukowa

Angielski

Artykuł

Hydrogen-bonded heterocomplexes formed by POOH-containing acids (diphenylphosphoric 1, dimethylphosphoric 2, diphenylphosphinic 3, and dimethylphosphinic 4) are studied by the low-temperature (100 K) ¹H-NMR and ³¹P-NMR using liquefied gases CDF₃/CDF₂Cl as a solvent. Formation of cyclic dimers and cyclic trimers consisting of molecules of two different acids is confirmed by the analysis of vicinal H/D isotope effects (changes in the bridging proton chemical shift, δH, after the deuteration of a neighboring H-bond). Acids 1 and 4 (or 1 and 3) form heterotrimers with very strong (short) H-bonds (δH ca. 17 ppm). While in the case of all heterotrimers the H-bonds are cyclically arranged head-to-tail, ···O=P–O–H···O=P–O–H···, and thus their cooperative coupling is expected, the signs of vicinal H/D isotope effects indicate an effective anticooperativity, presumably due to steric factors: when one of the H-bonds is elongated upon deuteration, the structure of the heterotrimer adjusts by shortening the neighboring hydrogen bonds. We also demonstrate the formation of cyclic tetramers: in the case of acids 1 and 4 the structure has alternating molecules of 1 and 4 in the cycle, while in case of acids 1 and 3 the cycle has two molecules of 1 followed by two molecules of 3.

phosphinic acids, phosphoric acids, hydrogen bond, heterodimers, heterotrimers, heterotetramers, H/D isotope effects, NMR

CC-BY

http://dx.doi.org/10.3390/molecules25081907

http://www.mdpi.com/journal/metals