Unexpected trends in halogen-bond based noncovalent adducts

Electronegativity Halogen bond Non-covalent interactions
DOI: 10.1039/c2cc33304j Publication Date: 2012-06-14T11:00:22Z
ABSTRACT
Unexpected trends in the strengths of halogen-bond based adducts CY(3)I (Y = F, Cl, Br, I) with two typical Lewis bases (chloride and trimethylamine) show that donor strength (Lewis acidity) a compound R-X is not necessarily increased higher electronegativity (carbon-based) group R.
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