Details
| Original language | English |
|---|---|
| Pages (from-to) | 1462-1463 |
| Number of pages | 2 |
| Journal | Journal of the American Chemical Society |
| Volume | 125 |
| Issue number | 6 |
| Publication status | Published - 12 Feb 2003 |
Abstract
A new molecular system combining an open-shell organic radical that acts as an acceptor group, different from an o-quinone moiety, covalently linked to a ferrocene moiety, acting as the donor group, is shown to exhibit valence tautomerism.
ASJC Scopus subject areas
- Chemical Engineering(all)
- Catalysis
- Chemistry(all)
- General Chemistry
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Chemical Engineering(all)
- Colloid and Surface Chemistry
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In: Journal of the American Chemical Society, Vol. 125, No. 6, 12.02.2003, p. 1462-1463.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - A new valence tautomerism example in an electroactive ferrocene substituted triphenylmethyl radical
AU - Ratera, Imma
AU - Ruiz-Molina, Daniel
AU - Renz, Franz
AU - Ensling, Jürgen
AU - Wurst, Klaus
AU - Rovira, Concepció
AU - Gütlich, Philipp
AU - Veciana, Jaume
PY - 2003/2/12
Y1 - 2003/2/12
N2 - A new molecular system combining an open-shell organic radical that acts as an acceptor group, different from an o-quinone moiety, covalently linked to a ferrocene moiety, acting as the donor group, is shown to exhibit valence tautomerism.
AB - A new molecular system combining an open-shell organic radical that acts as an acceptor group, different from an o-quinone moiety, covalently linked to a ferrocene moiety, acting as the donor group, is shown to exhibit valence tautomerism.
UR - http://www.scopus.com/inward/record.url?scp=0037433193&partnerID=8YFLogxK
U2 - 10.1021/ja0282590
DO - 10.1021/ja0282590
M3 - Article
C2 - 12568590
AN - SCOPUS:0037433193
VL - 125
SP - 1462
EP - 1463
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 6
ER -