Alcohol- and water-soluble bis(tpy)quaterthiophenes with phosphonium side groups: new conjugated units for metallo-supramolecular polymersElectronic supplementary information (ESI) available. See DOI: 10.1039/c5dt04133c

Bis( tpy )quaterthiophenes with symmetrically distributed two and four 6-bromohexyl side groups were prepared and modified by the reaction with triethylphosphine to give the corresponding ionic species. Both ionic and non-ionic bis( tpy )quaterthiophenes (unimers) were assembled with Zn 2+ and Fe 2+...

Full description

Saved in:
Bibliographic Details
Main Authors Štenclová, P, Šichová, K, Šloufová, I, Zedník, J, Vohlídal, J, Svoboda, J
Format Journal Article
Published 06.01.2016
Online AccessGet full text

Cover

Loading…
More Information
Summary:Bis( tpy )quaterthiophenes with symmetrically distributed two and four 6-bromohexyl side groups were prepared and modified by the reaction with triethylphosphine to give the corresponding ionic species. Both ionic and non-ionic bis( tpy )quaterthiophenes (unimers) were assembled with Zn 2+ and Fe 2+ ions to conjugated metallo-supramolecular polymers (MSPs), of which the ionic ones are soluble in alcohols and those derived from tetrasubstituted unimers are soluble even in water. The differences in assembly are specified between systems with (i) ionic and non-ionic unimers, (ii) Zn 2+ and Fe 2+ ion couplers, and (iii) methanol and water solvents. A substantial decrease in the stability of Fe-MSPs and a surprisingly high red shift of the luminescence band of Zn-MSPs were observed on going from methanol to aqueous solutions. Bis( tpy )quaterthiophenes with symmetrically distributed two and four 6-bromohexyl side groups were prepared and modified by the reaction with triethylphosphine to give the corresponding ionic species.
Bibliography:Electronic supplementary information (ESI) available. See DOI
10.1039/c5dt04133c
ISSN:1477-9226
1477-9234
DOI:10.1039/c5dt04133c