Cyclopentadienylruthenium π complexes of subphthalocyanines: A "drop-pin" approach to modifying the electronic features of aromatic macrocycles
Caballero E, Fernandez-Ariza J, Lynch VM, Nieto CR, Salome Rodriguez-Morgade M, Sessler JL, Guldi DM, Torres T (2012)
Publication Type: Journal article, Original article
Publication year: 2012
Journal
Original Authors: Caballero E., Fernandez-Ariza J., Lynch V.M., Romero-Nieto C., Rodriguez-Morgade M.S., Sessler J.L., Guldi D.M., Torres T.
Publisher: Wiley-VCH Verlag
Book Volume: 51
Pages Range: 11337-11342
Journal Issue: 45
Abstract
Facing facts: Coordination of Cp*Ru (Cp*=CMe ) to the concave and convex π surfaces of subphthalocyanines constitutes a new approach to the functionalization of subazaporphyrins. While the convex face shows higher reactivity, coordination to the concave side produces a stronger diatropic influence on the Cp* ligand and a greater perturbation of the macrocyclic π-electronic features. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Authors with CRIS profile
Involved external institutions
Universidad Autónoma de Madrid (UAM)
Spain (ES)
University of Texas at Austin
United States (USA) (US)
Spain (ES)
University of Texas at Austin
United States (USA) (US)
How to cite
APA:
Caballero, E., Fernandez-Ariza, J., Lynch, V.M., Nieto, C.R., Salome Rodriguez-Morgade, M., Sessler, J.L.,... Torres, T. (2012). Cyclopentadienylruthenium π complexes of subphthalocyanines: A "drop-pin" approach to modifying the electronic features of aromatic macrocycles. Angewandte Chemie International Edition, 51(45), 11337-11342. https://doi.org/10.1002/anie.201206111
MLA:
Caballero, Esmeralda, et al. "Cyclopentadienylruthenium π complexes of subphthalocyanines: A "drop-pin" approach to modifying the electronic features of aromatic macrocycles." Angewandte Chemie International Edition 51.45 (2012): 11337-11342.
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