Comparing C2=O and C2=S Barbiturates: Different Hydrogen-Bonding Patterns of Thiobarbiturates in Solution and the Solid State

• Published in: International journal of molecular sciences 2021-11, Vol.22 (23), p.12679
• Main Authors: Li, Chenming, Hilgeroth, Philipp, Hasan, Nazmul, Ströhl, Dieter, Kressler, Jörg, Binder, Wolfgang H
• Format: Article
• Language: English
• Subjects: (2-thio)barbiturates; Barbiturates; Barbiturates - chemistry; Brewster angle; Carbonyls; Coalescing; Comparative studies; Crystallization; Crystallography, X-Ray; Drugs; Free energy; Gibbs free energy; Hydrogen; Hydrogen Bonding; Hydrogen bonds; Hydrophobicity; Langmuir film; Models, Molecular; Molecular Conformation; Polyisobutylene; Polymers; Polymers - chemistry; Rheological properties; Spectrum analysis; supramolecular association; Temperature; Temperature dependence; Thiobarbiturates - chemistry
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms222312679

Carbonyl-centered hydrogen bonds with various strength and geometries are often exploited in materials to embed dynamic and adaptive properties, with the use of thiocarbonyl groups as hydrogen-bonding acceptors remaining only scarcely investigated. We herein report a comparative study of C2=O and C2=S barbiturates in view of their differing hydrogen bonds, using the 5,5-disubstituted barbiturate and the thiobarbiturate as model compounds. Owing to the different hydrogen-bonding strength and geometries of C2=O vs. C2=S, we postulate the formation of different hydrogen-bonding patterns in C2=S in comparison to the C2=O in conventional barbiturates. To study differences in their association in solution, we conducted concentration- and temperature-dependent NMR experiments to compare their association constants, Gibbs free energy of association , and the coalescence behavior of the N-H‧‧‧S=C bonded assemblies. In Langmuir films, the introduction of C2=S suppressed 2D crystallization when comparing and using Brewster angle microscopy, also revealing a significant deviation in morphology. When embedded into a hydrophobic polymer such as polyisobutylene, a largely different rheological behavior was observed for the barbiturate-bearing compared to the thiobarbiturate-bearing polymers, indicative of a stronger hydrogen bonding in the thioanalogue . We therefore prove that H-bonds, when affixed to a polymer, here the thiobarbiturate moieties in can reinforce the nonpolar PIB matrix even better, thus indicating the formation of stronger H-bonds among the thiobarbiturates in polymers in contrast to the effects observed in solution.