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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Be(CO)3 as a Nontraditional Lewis Base Engaging in Halogen Bonding
Zhaohui Jia1, Qingzhong Li1, Steve Scheiner2
1The Laboratory of Theoretical and Computational Chemistry, School of Chemistry and Chemical Engineering, Yantai University, Yantai 264005, P. R. China.
Abstract:
The HOMO of Be(CO)3 resembles a Be lone pair that can donate charge in the context of a halogen bond. This propensity is tested via quantum chemical calculations wherein Be(CO)3 is paired with XF, XCl, XCN, and XCF3 (X = I, Br, Cl). In the case of the latter two molecules where X is attached to C, a fully noncovalent halogen bond is formed that varies in strength between 2.2 and 9.7 kcal/mol. The bonding causes a stretch of the internal X-C bond and a red shift of its stretching frequency. Interactions with XF and XCl are much stronger, 40 kcal/mol and higher, containing strong elements of covalency. The bridging X atom in these complexes shifts a good deal toward the Be center in what may be classified as partial transfer or halogen sharing. In contrast to the noncovalent halogen bonds involving XCN and XCF3, where the interaction is strengthened as X grows larger, the opposite trend is observed for the halogen-shared complexes including XF and XCl.
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