Two branched polyphenylenes with 1,3,5-triphenylbenzene as branching centers were synthesized together with a family of phenylene cyclotrimers as model compounds. On the basis of the NMR analysis, specifically 1H NMR, 13C NMR and 2D heteronuclear correlation experiments (HSQC and HMBC) of model compounds, the huge number of overlapping signals in the polymer spectra are attributed to aromatic protons and carbon atoms of the branched phenylene structure. The comparison with absorption spectra of linear model compounds clearly shows that the polymer optical properties depend on the length of the segments between the branching cores. This result strongly supports the proposed NMR assignment proving that the combination of the two techniques is a powerful tool for unveiling complex branched structures.

Branched polyphenylenes and phenylene dendrimers:NMR and optical studies

Roberto Consonni;Umberto Giovanella;
2013

Abstract

Two branched polyphenylenes with 1,3,5-triphenylbenzene as branching centers were synthesized together with a family of phenylene cyclotrimers as model compounds. On the basis of the NMR analysis, specifically 1H NMR, 13C NMR and 2D heteronuclear correlation experiments (HSQC and HMBC) of model compounds, the huge number of overlapping signals in the polymer spectra are attributed to aromatic protons and carbon atoms of the branched phenylene structure. The comparison with absorption spectra of linear model compounds clearly shows that the polymer optical properties depend on the length of the segments between the branching cores. This result strongly supports the proposed NMR assignment proving that the combination of the two techniques is a powerful tool for unveiling complex branched structures.
2013
Istituto per lo Studio delle Macromolecole - ISMAC - Sede Milano
Polyphenylene dendrimers
1H 13C NMR -spectroscopy
Proton-carbon correlation experiments
Electronic absorption
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/214644
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