Wielopolski, MateuszMolina Ontoria, AgustínSchubert, ChristinaMargraf. Johannes T.Krokos, EvangelosKirschner, JohannesGouloumis, AndreasClark, TimothyGuldi, Dirk M.Martín León, Nazario2025-01-202025-01-202013-07-030002-78631520-512610.1021/ja401239rhttps://hdl.handle.net/20.500.14352/115116A series of ZnP-pCp-oPPV-C60 conjugates covalently connected through [2,2′]-paracyclophane-oligophenylenevinylene (pCp-oPPV) bridges containing one, two, and three [2,2′]-paracyclophanes (pCps) has been prepared in multistep synthetic procedures involving Horner-Wadsworth-Emmons olefination reactions and/or Heck type Pd-catalyzed reactions. Molecular modeling suggests that charge transfer is effectively mediated by the pCp-oPPVs through a predominant hole-transfer mechanism. Photophysical investigation supports molecular modeling and reveals two major trends. On one hand, C 60 excitation of 1, 2, and 3 leads exclusively to charge transfer between pCp and C60 to afford a ZnP-(pCp-oPPV)•+- C60•- radical ion pair state without giving rise to a subsequent charge shift to yield the ZnP•+-pCp-oPPV-C 60•- radical ion pair state. On the other hand, ZnP excitation of 1, 2, and 3 results in a rather slow charge transfer between ZnP and C60, after which the ZnP•+-pCp-oPPV-C 60•- radical ion pair state evolves. In temperature-dependent ZnP fluorescence experiments, which were performed in the temperature range from 273 to 338 K, two domains are discernible: low and high temperature behaviors. In the low temperature range (i.e., below 30 C) the rate constants do not change, suggesting that a superexchange mechanism is the modus operandi. In the high temperature range (i.e., >30 C) the rate constants increase. Moreover, we find rather strong distance dependence for 1 and 2 and weak distance dependence for 2 and 3. A damping factor of 0.145 Å-1 is derived for the former pair and 0.012 Å-1 for the latter.engAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/journal articlehttps://doi.org/10.1021/ja401239rhttps://pubs.acs.org/doi/10.1021/ja401239rrestricted access547AbsorptionAnionsCharge transferExcited statesFluorescenceQuímica orgánica (Química)2306 Química Orgánica