English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Electrochemical and spectrophotometric properties of polymers based on derivatives of di- and triphenylamines as promising materials for electronic applications.

MPS-Authors
/persons/resource/persons200157

Idzik,  K.
Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for biophysical chemistry, Max Planck Society;

External Resource
No external resources are shared
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Golba, S., Starczewska, O., & Idzik, K. (2015). Electrochemical and spectrophotometric properties of polymers based on derivatives of di- and triphenylamines as promising materials for electronic applications. Designed Monomers and Polymers, 18(8), 770-779. doi:10.1080/15685551.2015.1078110.


Cite as: http://hdl.handle.net/11858/00-001M-0000-002C-24BE-B
Abstract
Novel phenylamine-substituted derivatives, possessing different photochromic groups, were investigated. The electrochemical activity of the monomers and polymers were studied by usage of the electrochemical and spectroelectrochemical measurements. Heterocyclic side rings influence on the oxidation potential of monomers, decreasing its value below oxidation potential in comparison to parent phenylamine units. The removal of electron is easier for diphenylamine derivatives than for the triphenylamine ones. Electroactivity of monomers allows to polymerize them into macromolecule chains. Triphenylamine-based polymers are more stable as a result of the enlarged conjugated systems. Furthermore, the energy gap value of the final polymer can be reduced by introduction of additional branch into the monomer structure.