Synthesis of Novel π-Conjugated Polymers Having [2.2]Paracyclophane Skeleton in the Main Chain. Extension of π-Conjugated Length via the Through-Space
- 21 December 2001
- journal article
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 35 (3) , 587-589
- https://doi.org/10.1021/ma011170e
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Rigid rod conjugated polymers for nonlinear optics: 1. Characterization and linear optical properties of poly(aryleneethynylene) derivativesMacromolecules, 1994
- Synthesis and electrical properties of substituted paracyclophane polymersJournal of Polymer Science Part A: Polymer Chemistry, 1988
- Cyclopolymerization of (E,E) ‐ [6.2]paracyclophane‐1,5‐dieneJournal of Polymer Science Part A: Polymer Chemistry, 1986
- Synthesis of a new crystalline polymer: polymetacyclophaneJournal of the Chemical Society, Chemical Communications, 1985
- Polyaromatic ether‐sulfone‐ketones with fluorosubstituted p‐cyclophane units as crosslinking sitesJournal of Polymer Science: Polymer Chemistry Edition, 1983
- Cyclopolymerization of α,ω‐BIS(4‐vinylphenyl)‐alkane: Polymer containing [3.3] paracyclophane unit in the main chainJournal of Polymer Science Part C: Polymer Letters, 1976
- Aromatic polyethers, polysulfones, and polyketones as laminating resins. VII. Polymers with [2.2]‐p‐cyclophane unitsJournal of Polymer Science: Polymer Chemistry Edition, 1975
- Aromatic polyethers, polysulfones, and polyketones as laminating resins. IV. Polymers with p‐cyclophane units for crosslinkingJournal of Polymer Science: Polymer Chemistry Edition, 1975
- Paracyclophane units: Versatile segments for polymer chain crosslink formationJournal of Polymer Science Part B: Polymer Letters, 1972
- Macro rings. XXXVII. Multiple electrophilic substitution reactions of [2.2]paracyclophanes and interconversions of polysubstituted derivativesJournal of the American Chemical Society, 1969