Characterization of the ground state pyrene complex in ethylene‐propylene copolymer solutions

Abstract

AbstractPyrene‐labeled functionalized ethylene‐propylene (EP) copolymer was prepared by grafting 1‐pyrenebutyrylhydrazine onto EP copolymer through maleic anhydride pendants. The EP copolymer contained 60 mol % ethylene; its weight‐average molecular weight (Mw) was 148,000. The pyrene‐labeled amide functionalized EP copolymer, PA‐EP(60/40), was made to simulate the amine functionalized EP copolymers that are commonly used as dispersant additives in motor oils. UV absorption spectra, fluorescence emission and excitation spectra, and fluorescence decay profiles of the pyrene were studied to determine the copolymer conformation and dynamics in methylcyclohexane and tetrahydrofuran (THF). The pyrene fluorescence characteristics of PA‐EP(60/40) were highly dependent on the solvent. The dependence of fluorescence emission intensity on the excitation wavelength was large in methylcyclohexane and moderate in THF. A frequency shift of about 2 nm was observed between the excitation spectrum obtained with the emission line at 377 nm and that at 550 nm in the methylcyclohexane solutions, but no shift was found in the corresponding tetrahydrofuran solutions. The ratios of the preexponential factors (a21/a22) of the excimer decays obtained in both methylcyclohexane and THF solutions were different from −1.0. However, the deviation of the excimer formation process from the Birks scheme is small in THF but large in methylcyclohexane. In addition, the Huggins constants obtained from intrinsic viscosity measurements of the PA‐EP(60/40) copolymer solutions suggest that copolymer aggregation occurs in methylcyclohexane but not in THF. H‐bonding between two pyrene‐containing pendants is apparently the main driving force for the formation of the ground state pyrene complex. THF is found to be effective in inhibiting the H‐bonding formation. © 1995 John Wiley & Sons, Inc.