6, 6′, 11, 11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1, 4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization. Issue 5 (13th April 2017)

• Record Type: Journal Article
• Authors: Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd
• Is Part Of: Organic chemistry frontiers. Volume 4:Issue 5(2017)
• Page Start: 853
• Page End: 860
• Publication Date: 2017-04-13
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/c7qo00117g
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : [2.2]-Acenophanes are a class of compounds with two acene units interconnected by two ethano bridges. Abstract : [2.2]-Acenophanes are a class of compounds with two acene units interconnected by two ethano bridges. Due to the short bridges, the two acene subunits are in close proximity and can result in a modification of properties compared to the monomeric acene. We describe the synthesis of the first example of a [2.2](1, 4)tetracenophane that is modified by four (triisopropylsilyl)ethynyl substituents and its characterization by a number of techniques including single crystal X-ray crystallography. The tetracene moieties are found to be essentially parallel to each other in the molecule. The packing is characterized by the formation of a staircase arrangement with a weak overlap between individual tetracenophane molecules. Optical spectroscopy and electrochemical investigations indicate that the two tetracene moieties of the tetracenophane communicate more than the individual pentacene units in the larger pentacenophane.