Regulation of charge delocalization in a heteronuclear Fe2 ru system by a stepwise photochromic process.

Chemistry

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, 155 Yangqiao Road West, Fuzhou, Fujian 350002 (P.R. China).

Published: February 2015


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Article Abstract

Heteronuclear complexes FeCp2 -DTE-C≡C-Ru(dppe)2 Cl (1 o; dppe=1,2-bis(diphenylphosphino)ethane, Cp=cyclopentadienyl, DTE=dithienylethene) and FeCp2-DTE-C≡C-Ru(dppe)2-C≡C-DTE-FeCp2 (2 oo), with redox-active ferrocenyl and ruthenium centers separated by a photochromic DTE moiety, were prepared to achieve photoswitchable charge delocalization and Fe⋅⋅⋅Ru electronic communication. Upon UV-light irradiation of 2 oo, the Fe⋅⋅⋅Ru heterometallic electronic interaction is increasingly facilitated with stepwise photocyclization, 2 oo→2 co→2 cc; this is ascribed to the gradual increase in π-conjugated systems. The near-infrared absorptions in mixed-valence species [2 oo](+) /[2 co](+) /[2 cc](+) are gradually intensified following the conversion of [2 oo](+) →[2 co](+) →[2 cc](+) , which demonstrates that the extent of charge delocalization shows progressive enhancement with stepwise photocyclization. As revealed by electrochemical, spectroscopic, and theoretical studies, complex 2 exhibits nine switchable states through stepwise photochromic and reversible redox processes.

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