One-Electron Reduction of an “Extended Viologen” p-Phenylene-bis-4,4‘-(1-aryl-2,6-diphenylpyridinium) Dication-Reference-Cited by-同舟云学术

One-Electron Reduction of an “Extended Viologen” p-Phenylene-bis-4,4‘-(1-aryl-2,6-diphenylpyridinium) Dication

Published:2005-11-10 Issue:48 Volume:109 Page:10862-10869
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Funston Alison¹,Kirby James P.¹,Miller John R.¹,Pospíšil Lubomír¹,Fiedler Jan¹,Hromadová Magdaléna¹,Gál Miroslav¹,Pecka Jaroslav¹,Valášek Michal¹,Zawada Zbigniew¹,Rempala Pawel¹,Michl Josef¹

Affiliation:

1. Chemistry Department, Brookhaven National Laboratory, Building 555A, Upton, New York 11973, J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Dolejškova 3, 18223 Prague, Department of Organic Chemistry, Charles University, Albertov 2030, Prague, Czech Republic, and Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0215

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp053556n

Reference53 articles.

1. Oligomers of “Extended Viologen”, p-Phenylene-bis-4,4‘-(1-aryl-2,6-diphenylpyridinium), as Candidates for Electron-Dopable Molecular Wires

2. Charge Hopping in Molecular Wires as a Sequence of Electron-Transfer Reactions

3. Characterization of rigid rod poly(pyridinium salt)s by conformational analysis, molecular dynamics, and steady-state and time resolved fluorescence

4. Aromatic poly(pyridinium salt)s: synthesis and structure of organo-soluble, rigid-rod poly(pyridinium tetrafluoroborate)s

5. Aromatic poly(pyridinium salt)s Part 2. Synthesis and properties of organo-soluble, rigid-rod poly(pyridinium triflate)s

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