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RESEARCH PRODUCT
Water-Soluble Squaramide Dihydrates: N-Methylation Modulates the Occurrence of One- and Two-Dimensional Water Clusters through Hydrogen Bonding and Dipolar Interactions
Marta XimenisCarmen RotgerJavier Pitarch-jarqueEnrique García-españaAntonio CostaSalvador Blascosubject
010405 organic chemistryHydrogen bondChemistrySquaramideGeneral ChemistryCrystal structureN methylation010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesDipoleWater solubleChemical physicsMoleculeMoietyGeneral Materials Sciencedescription
Water confined in molecular size domains is distinct to bulk water. The altered interactions between adjacent water molecules, and between water molecules and molecular wall components of the confinement system, determine aspects of important phenomena in material science, biology, and nanotechnology. The structural determination of confined water, however, has proven to be challenging. Here, we describe the crystal structures of three related squaramides 1–3 whose molecular structures are modulated by the gradual incorporation of N-methyl groups to the squaramide moiety. The three squaramides differ in their hydrogen bonding capabilities due to the different degree of N-methylation of each one. Thus, while 1·2H2O forms narrow tapes of water molecules, the monomethylated squaramide 2·2H2O produces two-dimensional water layers, and the dimethylated squaramide 3·2H2O develops polymeric one-dimensional water chains. Our observations show that N-methylation heavily alters the interplay between H-bonding and d...
year | journal | country | edition | language |
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2018-07-10 | Crystal Growth & Design |