Krokos E, Spänig F, Ruppert M, Hirsch A, Guldi DM (2012)
Publication Type: Journal article, Original article
Publication year: 2012
Original Authors: Krokos E., Spänig F., Ruppert M., Hirsch A., Guldi D.M.
Publisher: Wiley-VCH Verlag
Book Volume: 18
Pages Range: 1328-1341
Journal Issue: 5
A series of truly water-soluble C60/porphyrin electron donor-acceptor conjugates has been synthesized to serve as powerful mimics of photosynthetic reaction centers. To this end, the overall water-solubility of the conjugates was achieved by adding hydrophilic dendrimers of different generations to the porphyrin moiety. An important variable is the metal center of the porphyrin; we examined zinc(II), copper(II), cobalt(II), nickel(II), iron- (III), and manganese (III). The first insights into electronic communication between the electron donors and the electron acceptors came from electrochemical assays, which clearly indicate that the redox processes centered either on C60 or the porphyrins are mutually affected. Absorption measurements, however, revealed that the electronic communication in terms of, for example, charge-transfer features, remains spectroscopically invisible. The polar environment that water provides is likely to be a cause of the lack of detection. Despite this, transient absorption measurements confirm that intramolecular charge separation processes in the excited state lead to rapid deactivation of the excited states and, in turn, afford the formation of radical ion pair states in all of the investigated cases. Most importantly, the lifetimes of the radical ion pairs were found to depend strongly on several aspects. The nature of the coordinated metal center and the type of dendrimer have a profound impact on the lifetime. It has been revealed that the nature/electronic configuration of the metal centers is decisive in powering a charge recombination that either reinstates the ground state or any given multiplet excited state. Conversely, the equilibrium of two opposing forces in the dendrimers, that is, the interactions between their hydrophilic regions and the solvent and the electronic communication between their hydrophobic regions and the porphyrin and/or fullerene, is the key to tuning the lifetimes. © 2012 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.
APA:
Krokos, E., Spänig, F., Ruppert, M., Hirsch, A., & Guldi, D.M. (2012). A charge-transfer challenge: Combining fullerenes and metalloporphyrins in aqueous environments. Chemistry - A European Journal, 18(5), 1328-1341. https://dx.doi.org/10.1002/chem.201102851
MLA:
Krokos, Evangelos, et al. "A charge-transfer challenge: Combining fullerenes and metalloporphyrins in aqueous environments." Chemistry - A European Journal 18.5 (2012): 1328-1341.
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