Both the copper(I) and copper(II) states exhibit coordinative ambiguity as well as a typically increased coordination no. after oxidn. This tendency can be used in dynamic redox systems, employing hemilabile innocent ligands. With noninnocent hemilabile ligands such as thioether- or selenoether-substituted o-semiquinone imines there is a complementary reactivity on the ligand side, viz., stepwise electron transfer and coordinative ambivalence. Some resulting combinations have been analyzed for two systems, involving one copper center and one camphorquinone imine or two o-benzoquinone imine components (Qn). Combining redox (CuI/II, Q0/·-/2-) and coordinatively ambivalent metal and ligand components (hemilability) creates variable electronic situations which require exptl. and theor. anal. on SciFinder(R)
%0 Journal Article
%1 Kaim.2018
%A Kaim, Wolfgang
%A Beyer, Katharina
%A Filippou, Vasileios
%A Zalis, Stanislav.
%D 2018
%J Coordination Chemistry Reviews
%K imported
%P 173--179
%R 10.1016/j.ccr.2017.08.006
%T Charge and spin coupling in copper compounds with hemilabile noninnocent ligands - Ambivalence in three dimensions
%V 355
%X Both the copper(I) and copper(II) states exhibit coordinative ambiguity as well as a typically increased coordination no. after oxidn. This tendency can be used in dynamic redox systems, employing hemilabile innocent ligands. With noninnocent hemilabile ligands such as thioether- or selenoether-substituted o-semiquinone imines there is a complementary reactivity on the ligand side, viz., stepwise electron transfer and coordinative ambivalence. Some resulting combinations have been analyzed for two systems, involving one copper center and one camphorquinone imine or two o-benzoquinone imine components (Qn). Combining redox (CuI/II, Q0/·-/2-) and coordinatively ambivalent metal and ligand components (hemilability) creates variable electronic situations which require exptl. and theor. anal. on SciFinder(R)
@article{Kaim.2018,
abstract = {Both the copper(I) and copper(II) states exhibit coordinative ambiguity as well as a typically increased coordination no. after oxidn. This tendency can be used in dynamic redox systems, employing hemilabile innocent ligands. With noninnocent hemilabile ligands such as thioether- or selenoether-substituted o-semiquinone imines there is a complementary reactivity on the ligand side, viz., stepwise electron transfer and coordinative ambivalence. Some resulting combinations have been analyzed for two systems, involving one copper center and one camphorquinone imine or two o-benzoquinone imine components (Qn). Combining redox (CuI/II, Q0/·-/2-) and coordinatively ambivalent metal and ligand components (hemilability) creates variable electronic situations which require exptl. and theor. anal. [on SciFinder(R)]},
added-at = {2022-06-15T11:26:56.000+0200},
author = {Kaim, Wolfgang and Beyer, Katharina and Filippou, Vasileios and Zalis, Stanislav.},
biburl = {https://puma.ub.uni-stuttgart.de/bibtex/229208dff831dbcaadad2c22772761e00/huebleriac},
doi = {10.1016/j.ccr.2017.08.006},
interhash = {662228f130d725b9096383ffda56eb31},
intrahash = {29208dff831dbcaadad2c22772761e00},
issn = {0010-8545},
journal = {Coordination Chemistry Reviews},
keywords = {imported},
pages = {173--179},
timestamp = {2022-06-15T09:26:56.000+0200},
title = {Charge and spin coupling in copper compounds with hemilabile noninnocent ligands - Ambivalence in three dimensions},
volume = 355,
year = 2018
}
