The influence of competitive interactions on multiple eutectic phase behavior in poly(ethylene oxide) molecular complexes

Binary mixtures of poly(ethylene oxide) and resorcinol exhibit two eutectic phase transitions at 40 and 80 degreesC, which are separated by a single-phase stoichiometric complex at approximate to33 mol% resorcinol. These eutectic temperatures increase slightly at higher molecular weights of poly(ethylene oxide). The eutectics and the molecular complex are absent in ternary mixtures with either 25 or 40 wt% poly(2-vinylpyridine) because both polymers contain electron-pair donors which participate in hydrogen bonding interactions with the hydroxyl groups of the small-molecule aromatic. In contrast, 25 wt% polystyrene does not disrupt the bi-eutectic phase behavior of poly(ethylene oxide) and resorcinol because polystyrene is inert in these ternary mixtures. The lightest lanthanides with the largest ionic radii in the first-row of the f-block, like LaCl3(H2O)(6) and CeCl3(H2O)(x), are more effective than neodymium, terbium and ytterbium trichloride hexahydrates from the viewpoint of (i) competing with resorcinol, (ii) interacting with poly(ethylene oxide), (iii) eliminating eutectic melting, and (iv) disrupting the 2:1 stoichiometric complex between poly(ethylene oxide) and resorcinol. High-resolution C-13 solid state NMR spectroscopy identifies resorcinol in several different molecular environments. Multiple resonances are observed for chemically equivalent, but morphologically and crystallographically inequivalent, C-13 sites in the solid state. The isotropic chemical shift of the phenolic C-13 site in this small-molecule aromatic is very sensitive to the strength of intermolecular interactions in various phases. For example, self-association of resorcinol in pure crystalline phase gamma yields a phenolic carbon chemical shift at 155 ppm. The formation of a 2:1 stoichiometric complex between poly(ethylene oxide) and resorcinol in co-crystallized phase beta is identified by a phenolic carbon chemical shift at 158 ppm. When resorcinol and poly(2-vinylpyridine) interact in a homogeneous amorphous phase, the phenolic carbon resonance appears at a chemical shift of 160 ppm. A resorcinol-rich disordered crystalline phase in ternary mixtures with poly(ethylene oxide) and poly(2-vinylpyridine) yields a phenolic carbon resonance at 159 ppm. Temperature-composition projections of the binary and ternary phase diagrams, constructed via differential scanning calorimetry. allow one to interpret C-13 NMR spectra of these strongly interacting blends and complexes in the solid state. (C) 2003 Elsevier Science Ltd. All rights reserved.