Abstract
In this paper we show that linked bis-isophthalic acid derivatives form ordered molecular structures in the solid state. The key organizing interactions are hydrogen bonds between the isophthalate carboxylic acid substituents on adjacent molecules or to methanol solvent. NMR investigations suggest that alternative aggregates form in solution.
Original language | English (US) |
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Pages (from-to) | 2327-2330 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 37 |
Issue number | 14 |
DOIs | |
State | Published - Apr 1 1996 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry