Dinuclear ruthenium acetylide complexes with diethynylated anthrahydroquinone and anthraquinone frameworks: a multi-stimuli-responsive organometallic switch. Issue 21 (8th May 2019)

• Record Type: Journal Article
• Authors: Oyama, Yousuke; Kawano, Reo; Tanaka, Yuya; Akita, Munetaka
• Is Part Of: Dalton transactions. Volume 48:Issue 21(2019)
• Page Start: 7432
• Page End: 7441
• Publication Date: 2019-05-08
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c9dt01255a
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : The organometallic AcAHQ/AQ-Ru system turns out to be an effective redox and pH stimuli triggered bimodal molecular switch. Abstract : The anthrahydroquinone (AHQ)/anthraquinone (AQ) system is of particular interest as a molecular switching system for molecule-based devices because AHQ and AQ can be interconverted by redox stimuli and their π-conjugated systems are distinct from each other. To date, however, a way to modify and/or functionalize the switching behavior based on the AHQ/AQ system is still limited. In the present contribution, the synthesis and properties of multi-responsive dinuclear molecular switches having Ru(dppe)2 fragments bridged by the diethynylated diacetoxyanthracene (AcAHQ) and AQ units (μ-AcAHQ/AQ){CC-Ru(R)(dppe)2 }2 (R = Cl, C4 TMS) are presented. The terminal Ru(dppe)2 fragments are redox-active and, therefore, the intermetallic interaction can be estimated by electrochemical as well as IVCT band analysis. As a result, the organometallic AcAHQ/AQ-Ru system turns out to be an effective bimodal molecular switch, which is triggered not only by redox stimuli but also by pH stimuli.