Pancake Bonding in π‐Stacked Trimers in a Salt of Tetrachloroquinone Anion

• Published in: Chemistry : a European journal 2018-06, Vol.24 (33), p.8292-8297
• Main Authors: Molčanov, Krešimir, Mou, Zhongyu, Kertesz, Miklos, Kojić‐Prodić, Biserka, Stalke, Dietmar, Demeshko, Serhiy, Šantić, Ana, Stilinović, Vladimir
• Format: Article
• Language: English
• Subjects: Bonding; Charge density; charge transfer; Chemistry; Crystal structure; Crystals; density functional calculations; Density functional theory; Diamagnetism; Insulators; Moisture content; pancake bonding; tetrachloroquinone; Trimers; X-ray charge density
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.201800672

The crystal structure of [4‐damp])2[Cl4Q]3 (4‐damp=4‐dimethylamino‐N‐methylpyridinium, Cl4Q=tetrachloroquinone) salt is built up from slipped columnar stacks of quinoid rings composed of closely bound trimers with the intra‐trimer separation distance of 2.84 Å and total charge of −2 whereas the inter‐trimer distance is 3.59 Å. The individual rings exhibit partial negative charges that are distributed unevenly among the three Cl4Qs in the trimer. The strong interactions within a trimer (Cl4Q)32− have a partially covalent character with two‐electron/multicentered bonding, that is extended over three rings, plausibly termed as “pancake bonding”. The electron pairing within this multicentre bond leads to the fact that the crystals are diamagnetic and act as insulators. The studies of the structure and nature of bonding are based on X‐ray charge density analysis and density functional theory. Bonding over breakfast? Partially covalent pancake bonding in a trimer of partially charged tetrachloroquinone molecules (total charge −2) is studied by a combination of X‐ray charge density analysis and DFT calculations. Separation distance between the rings in a trimer is 2.84 Å.