2006
DOI: 10.1295/polymj.pj2005218
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Synthesis and Characterization of Main Chain Polyimides Containing Chalcone Derivatives for LC Alignment

Abstract: ABSTRACT:Two soluble polyimides containing chalcone derivatives in the main chains were successfully prepared using the Mitsunobu reaction at room temperature, reacting diols with diimides. With this reaction procedure the high temperature imidization step normally needed for the synthesis of polyimides is avoided and the polymers can be used for temperature sensitive applications. The main chain polyimides were characterized with FT-IR, NMR and DSC and the extent of the photoreaction was measured with FT-IR a… Show more

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Cited by 10 publications
(3 citation statements)
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“…These derivatives might be useful in single molecule fluorescence imaging . Polyimides that can be coated on films and show optical anisotropy have been synthesized at room temperature by the reaction of diols with diimides using the Mitsunobu protocol . This procedure was deemed useful for temperature sensitive applications.…”
Section: Amines Amides (Including Nucleobases) or Azides As Nucleophilesmentioning
confidence: 99%
“…These derivatives might be useful in single molecule fluorescence imaging . Polyimides that can be coated on films and show optical anisotropy have been synthesized at room temperature by the reaction of diols with diimides using the Mitsunobu protocol . This procedure was deemed useful for temperature sensitive applications.…”
Section: Amines Amides (Including Nucleobases) or Azides As Nucleophilesmentioning
confidence: 99%
“…[19] Thesuccessful removal of PEO and crosslinking of PChal through UV treatment are further demonstrated by IR spectroscopy (Supporting Information, Figure S4 B). [21] Carboxyl groups are generated after cleavage of the ONB group,asevidenced by the appearance of ab road peak at 3300 cm À1 . [15h, 20] Both of these peaks disappear after removal of the PEO.T he photo-crosslinking of the chalcone mesogens is also verified by the disappearance of the peaks at 1660 and 1587 cm À1 ,w hich correspond to C = Oa nd C = C groups,respectively,after UV irradiation.…”
mentioning
confidence: 99%
“…[15h, 20] Both of these peaks disappear after removal of the PEO.T he photo-crosslinking of the chalcone mesogens is also verified by the disappearance of the peaks at 1660 and 1587 cm À1 ,w hich correspond to C = Oa nd C = C groups,respectively,after UV irradiation. [21] Carboxyl groups are generated after cleavage of the ONB group,asevidenced by the appearance of ab road peak at 3300 cm À1 .…”
mentioning
confidence: 99%