SYNTHESIS OF MONODISPERSE MACROMOLECULAR BICYCLIC AND DENDRITIC COMPOUNDS FROM (R)-3-HYDROXYBUTANOIC ACID AND BENZENE-1,3,5-TRICARBOXYLIC ACID AND ANALYSIS BY FRAGMENTING MALDI-TOF MASS SPECTROSCOPY

摘要

As previously shown, oligo- and poly(beta-hydroxyalkanoates) have a high tendency to form lamellar crystallites with ca. 50-Angstrom thickness which corresponds to chain lengths of 16 units (Fig. I). To have monodisperse model compounds, we have now prepared bicyclic derivatives with three parallel (27-29) or two parallel and an antiparallel chain (68-70) consisting of up to 16 3-hydroxybutanoate (3-HB) units. We also prepared dendritic compounds (71-75, 82-85) containing oligo(3-HB) chains which cannot possibly be arranged as in the lamellae; the branching units were prepared from trimesic acid (= benzene-1,3,5-tricarboxylic acid). So far, none of the prepared samples formed crystals or contained crystalline domains which would have been suitable for single-crystal or powder-diffraction X-ray analysis. The terminally deprotected dendrimers (74, 75, and 85) are multi-anionic (up to 12 peripheral CO2H groups) and biodegradable. The macromolecular HE derivatives (molecular weight up to 10150 Da) have been fully characterized by IR, H-1- and C-13-NMR, [alpha](D), and elemental analysis. Especially important is the analysis by mass spectrometry with the MALDI-TOF technique (Fig. 2), proving that the products are monodisperse; application of a new variation of this MS method (post source decay = PSD or fragment analysis by structural lime of flight = FAST(TM)) allows for the observation of metastable fragment ions and, thus, is a tool for structural oligomer analysis (Fig. 3). [References: 88]