Intramolecular excimer formation in model compounds for polyesters. Diesters from 2-naphthol and aliphatic dicarboxylic acids
Author:
Publisher
Elsevier BV
Subject
Polymers and Plastics,Materials Chemistry,Organic Chemistry
Reference21 articles.
1. Dependence of the occupancy of excimer-forming conformations on the size of the flexible spacer in polyesters from terephthalic acid and mono-, di- or triethylene glycol
2. Identification of conformations conducive to intramolecular excimer formation in polyesters with different numbers of methylene units between aromatic rings
3. Intramolecular excimer formation by phthaloyl, isophthaloyl and terephthaloyl groups in polyesters with different numbers of methylene and oxyethylene spacers
4. Dynamics of conformational transitions to isomeric states favoring intramolecular excimer formation in aromatic polyesters with methylene or oxyethylene spacers
5. Patel, B., Mendicuti, F. and Mattice, W. L. Polymer in press
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3. Fluorescence Properties of Poly(ethylene terephthalate-co-2,6-naphthalene dicarboxylate) with Naphthalene Contents Ranging from 0.01 to 100 mol;Macromolecules;1999-04-06
4. Intramolecular excited state complexes in trichromophoric model compounds for polyesters derived from 2,6-naphthalenedicarboxylic acid and aliphatic glycols: experiment, rotational isomeric state model, and molecular dynamics;Journal of Polymer Science Part B: Polymer Physics;1999-02-01
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