The two-dimensional pattern formation of hydrogen bonding isophthalic acid derivatives at the liquid/solid interface has been investigated using scanning tunneling microscopy. By varying the location and nature of alkyl substituents on the aromatic core in combination with the intrinsic hydrogen bonding properties of the isophthalic acid units, the two-dimensional supramolecular ordering has been controlled, leading to several different motifs.
No takes yet. Share an insight, caveat, or question.
Feyter et al. (2003) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: