The significance of the alkene size and the nature of the metal ion in metalalkene complexes: a theoretical studyElectronic supplementary information (ESI) available: optimized geometries, total energies, EDA and NBO results. See DOI: 10.1039/c2dt30119a

Cation interactions with -systems are a problem of outstanding contemporary interest and the nature of these interactions seems to be quite different for transition and main group metal ions. In this paper, we have systematically analyzed the contrast in the bonding of Cu + and main group metal ions. The molecular structures and energetics of the complexes formed by various alkenes (A = C n H 2 n , n = 26; C n H 2 n 2 , n = 38 and C n H 2 n + 2 , n = 510) and metal ions ( M = Li + , Na + , K + , Ca 2+ , Mg 2+ , Cu + and Zn 2+ ) are investigated by employing ab initio post HartreeFock (MP2/6-311++G**) calculations and are reported in the current study. The study, which also aims to evaluate the effect of the size of the alkyl portion attached to the -system on the complexation energy, indicates a linear relationship between the two. The decreasing order of complexation energy with various metal ionalkene complexes follows the order Zn 2+ A > Mg 2+ A > Ca 2+ A > Cu + A > Li + A > Na + A > K + A . The increased charge transfer and the electron density at (3,1) intermolecular bond critical point corroborates well with the size of the -system and the complexation energy. The observed deviation from the linear dependency of the Cu + A complexes is attributed to the d * back bonding interaction. An energy decomposition analysis via the reduced variational space (RVS) procedure was also carried out to analyze which component among polarization, charge transfer, coulomb and exchange repulsion contributes to the increase in the complexation energy. The RVS results suggest that the polarization component significantly contributes to the increase in the complexation energy when the alkene size increases. The impact of the size of the alkene and the nature of the metal ion in metalalkene complexes.