Abstract
Unexpected trends in the strengths of halogen-bond based adducts of CY3I (Y = F, Cl, Br, I) with two typical Lewis bases (chloride and trimethylamine) show that the halogen-bond donor strength (Lewis acidity) of a compound R–X is not necessarily increased with higher electronegativity of the (carbon-based) group R. © 2012 Royal Society of Chemistry.
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CITATION STYLE
APA
Huber, S. M., Jimenez-Izal, E., Ugalde, J. M., & Infante, I. (2012). Unexpected trends in halogen-bond based noncovalent adducts. Chemical Communications, 48(62), 7708–7710. https://doi.org/10.1039/c2cc33304j
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