Dynamics of conformational transitions to isomeric states favoring intramolecular excimer formation in aromatic polyesters with methylene or oxyethylene spacers
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.456297
Reference21 articles.
1. Dynamics of conformational transitions to isomeric states favoring intramolecular excimer formation in polymeric chains. Application to dimer models of polystyrene
2. Mobility of macromolecular chains as studied by means of excimer fluorescence
3. Mobility of macromolecular chains as studied by means of excimer fluorescence
4. 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
5. Identification of conformations conducive to intramolecular excimer formation in polyesters with different numbers of methylene units between aromatic rings
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1. Structure—Property Relationships of Aromatic Polyesters;KOBUNSHI RONBUNSHU;2010
2. Conformational Characteristics, Configurational Properties, and Thermodynamic Characteristics of Poly(ethylene terephthalate) and Poly(ethylene-2,6-naphthalate);Macromolecules;2009-03-18
3. Morphological Consequences of Interchange Reactions during Solid State Polymerization in Oriented Polymers;Macromolecules;2001-05-11
4. Elucidation of the Chain Conformation in a Glassy Polyester, PET, by Two-Dimensional NMR;Science;1998-05
5. Rationalization of the ratio of excimer-to-monomer fluorescence emission intensity in bichromophoric diesters of 1-pyrenoic acid and mono-, di-, tri-, and tetraethylene glycols;Journal of Polymer Science Part B: Polymer Physics;1995-05
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