The Dominant Role of Chalcogen Bonding in the Crystal Packing of 2D/3D Aromatics

0434589 - ÚOCHB 2015 RIV DE eng J - Journal Article
Fanfrlík, Jindřich - Přáda, A. - Padělková, Z. - Pecina, Adam - Macháček, Jan - Lepšík, Martin - Holub, Josef - Růžička, A. - Hnyk, Drahomír - Hobza, Pavel
The Dominant Role of Chalcogen Bonding in the Crystal Packing of 2D/3D Aromatics.
Angewandte Chemie - International Edition. Roč. 53, č. 38 (2014), s. 10139-10142. ISSN 1433-7851. E-ISSN 1521-3773
R&D Projects: GA ČR GBP208/12/G016; GA ČR GAP208/10/2269
Grant - others:GA MŠk(CZ) ED2.1.00/03.0058; GA MŠk(CZ) ED1.1.00/02.0070; GA MŠk(CZ) LM2011033
Program: ED; ED
Institutional support: RVO:61388963 ; RVO:61388980
Keywords : boranes * chalcogen bonds * crystal structures * sulfur * X-ray diffraction
Subject RIV: CF - Physical ; Theoretical Chemistry
Impact factor: 11.261, year: 2014

The chalcogen bond is a nonclassical sigma-hole-based noncovalent interaction with emerging applications in medicinal chemistry and material science. It is found in organic compounds, including 2D aromatics, but has so far never been observed in 3D aromatic inorganic boron hydrides. Thiaboranes, harboring a sulfur heteroatom in the icosahedral cage, are candidates for the formation of chalcogen bonds. The phenylsubstituted thiaborane, synthesized and crystalized in this study, forms sulfur center dot center dot center dot pi type chalcogen bonds. Quantum chemical analysis revealed that these interactions are considerably stronger than both in their organic counterparts and in the known halogen bond. The reason is the existence of a highly positive sigma-hole on the positively charged sulfur atom. This discovery expands the possibilities of applying substituted boron clusters in crystal engineering and drug design.
Permanent Link: http://hdl.handle.net/11104/0238582