Publication Type Journal Article
Title ESR and ENDOR investigations on various Wurster s radical cations in solution. Experimental results, theoretical ab initio, and DFT calculations
Authors G Grampp AM Kelterer S Landgraf M Sacher D Niethammer J. P. Telo RMB Dias AJSC Vieira
Groups
Journal MONATSHEFTE FUR CHEMIE
Year 2005
Month April
Volume 136
Number 4
Pages 519-536
Abstract ESR and ENDOR spectra are reported of several symmetrical substituted N,N,N ,N -tetraalkyl-p-phenylenediamine radical cations in solution. Different N,N -alkyl substituted paraphenylenediamines, like the ethyl, n-propyl, and iso-propyl derivative are compared with the parent N,N,N, ,N -tetramethyl-p-phenylenediamine (Wurster s Blue Cation). N,N,N ,N -Tetrabenzyl-p-phenylenediamine, 1,4-dipyrrolidinylbenzene, and N,N -bis[4-(dimethylamino)phenyllpiperazine are additionally investigated. Experimental and calculated hyperfine coupling constants are compared. Characteristic UV-VIS data and redox potentials in acetonitrile are reported, together with the syntheses of the compounds.
DOI http://dx.doi.org/10.1007/s00706-004-0224-4
ISBN
Publisher SPRINGER WIEN
Book Title
ISSN 0026-9247
EISSN
Conference Name
Bibtex ID ISI:000228694100002
Observations
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