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Implications of Guanidine Substitution on Copper Complexes as Entatic‐State Models
Author(s) -
Hoffmann Alexander,
Stanek Julia,
Dicke Benjamin,
Peters Laurens,
GrimmLebsanft Benjamin,
Wetzel Alina,
Jesser Anton,
Bauer Matthias,
Gnida Manuel,
MeyerKlaucke Wolfram,
Rübhausen Michael,
HerresPawlis Sonja
Publication year - 2016
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201600655
Subject(s) - chemistry , guanidine , steric effects , copper , crystallography , ligand (biochemistry) , coordination sphere , trifluoromethanesulfonate , computational chemistry , crystal structure , stereochemistry , organic chemistry , biochemistry , receptor , catalysis
The guanidine–quinoline ligand dimethylethyleneguanidinoquinoline (DMEGqu) is able to stabilise bis(chelate) copper complexes in an intermediate geometry between tetrahedral and square‐planar environments. The structures of the obtained complexes model the entatic state and have been investigated in solid state by single‐crystal X‐ray diffraction and in the solid state and in solution by X‐ray absorption spectroscopy. The dimethylethyleneguanidine (DMEG) unit of the DMEGqu ligand displays a smaller steric encumbrance than the tetramethylguanidine (TMG) counterpart; this allows slightly larger structural changes upon oxidation than those for the TMG counterparts. Moreover, triflate coordination was possible for the Cu II DMEG complexes. DFT analyses revealed that good structural and optical descriptions are possible through the use of the hybrid functionals B3LYP and TPSSh in combination with the triple‐zeta basis set def2‐TZVP and the inclusion of empirical dispersion with Becke–Johnson damping and a suitable solvent model. The orbital analysis gives insights into the electronic structure of the complexes and their charge‐transfer behaviour.