Analyzing the molecular weight distribution in supramolecular polymers

S.A. Schmid, R.J. Abbel, A.P.H.J. Schenning, E.W. Meijer, R.P. Sijbesma, L.M. Herz

Research output: Contribution to journalArticleAcademicpeer-review

27 Citations (Scopus)
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Abstract

We have investigated the formation process of supramolecular linear polymer chains and its influence on the resulting chain length distribution function. For this purpose, we explored the migration of excitation energy between oligofluorene units coupled together through quadruple hydrogen-bonding groups to form linear chains that are terminated by oligophenylene vinylene end-caps acting as energy traps. The energy transfer dynamics from the main chain to the chain end was monitored experimentally using time-resolved PL spectroscopy and compared to an equivalent Monte Carlo simulation incorporating information on the structure of the chains, the transition transfer rates, and various weight distribution trial functions. We find that the assumption of a Flory distribution of chain lengths leads to excellent agreement between experimental and simulated data for a wide range of end-cap concentrations. On the other hand, both a Poisson function and a simplified assumption of a monodisperse distribution significantly underestimate the presence of long chains in the ensemble. Our results therefore show that supramolecular polymerization is a steplike process equivalent to polycondensation reactions in linear covalent polymers. These findings emphasize that equal reactivity of the supramolecular building blocks leads to a dynamic growth process for the supramolecular chain involving all chain components at all times. ©2009 American Chemical Society.
Original languageEnglish
Pages (from-to)17696-17704
JournalJournal of the American Chemical Society
Volume131
Issue number48
DOIs
Publication statusPublished - 2009

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