@article{oai:oist.repo.nii.ac.jp:00002778,
 author = {Karimata, Ayumu and Gridneva, Tatiana and Patil, Pradnya H. and Fayzullin, Robert R. and Khaskin, Eugene and Lapointe, Sébastien and Garcia-Roca, Alèria and Khusnutdinova, Julia R.},
 issue = {35},
 journal = {Dalton Transactions},
 month = {Aug},
 note = {Herein we report a series of CuI complexes supported by tetradentate RN4 pyridinophane ligands that coordinate to ethylene forming either mononuclear complexes with ethylene coordinated in an η2-mode or a binuclear complex where ethylene binds to two Cu atoms in a μ-η2-η2-mode, depending on the steric effects of the RN4 ligand and the reaction conditions. In the binuclear complex with bridging ethylene, the C[double bond, length as m-dash]C bond is significantly elongated, with a bond length of 1.444(8) Å according to X-ray diffraction analysis. This complex represents the only examination a μ-η2-η2-coordinated Cu–olefin complex reported to date, featuring one of the longest reported C[double bond, length as m-dash]C bonds. The spectroscopic characterization, structure, electrochemical properties and solution behavior are analyzed in this study. Coordination of ethylene was found to be reversible in these complexes and more favored in less sterically hindered RN4 ligands, so that ethylene binding is observed in a coordinating solvent (MeCN) environment. In the case of the MeN4 ligand, the ethylene complex is photoluminescent in the solid state. The ethylene binding modes in mono- and binuclear complexes are elucidated through Natural Bond Orbital and QTAIM analyses.},
 pages = {13426--13434},
 title = {Ethylene binding in mono- and binuclear CuI complexes with tetradentate pyridinophane ligands},
 volume = {51},
 year = {2022}
}