Abstract
Pseudopara[2.2]paracyclophane- and [2.1]orthocyclophane-bridged diruthenium complexes 2 and 3 with two interlinked electroactive styryl ruthenium moieties have been prepared and investigated. Both complexes undergo two reversible consecutive one-electron oxidation processes which are separated by 270 or 105 mV. Stepwise electrolysis of the neutral complexes to first the mixed-valent radical cations and then the dioxidized dications under IR monitoring reveal incremental shifts of the charge-sensitive Ru(CO) bands and allow for an assignment of their radical cations as moderately or very weakly coupled mixed-valent systems of class II according to Robin and Day. Ground-state delocalization in the mixed-valent forms of these complexes as based on the CO band shifts is considerably larger for the "closed" paracyclophane as for the "half-open" orthocyclophane. Experimental findings are backed by the calculated IR band patterns and spin density distributions for radical cations of slightly simplified model complexes 2Me*+ and 3Me*+ with the PiPr3 ligands replaced by PMe3. Radical cations 2*+ and 3*+ feature a characteristic NIR band that is neither present in their neutral or fully oxidized forms nor in the radical cation of the monoruthenium[2.2]paracyclophane complex 1 with just one vinyl ruthenium moiety. These bands are thus assigned as intervalence charge transfer (IVCT) transitions. Our results indicate that, for the radical cations, electronic coupling "through space" via the stacked styrene decks is significantly more efficient than the "through-bond" pathway.