Copper Complexes with Neutral N4 Tripodal Ligands: Influence of the Number of Nitrogen Donors on Their Structures, Properties, and Reactivity
✍ Scribed by Kiyoshi Fujisawa; Shingo Chiba; Yoshitaro Miyashita; Ken-ichi Okamoto
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 345 KB
- Volume
- 2009
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
Abstract
Copper coordination complexes of the neutral tetradentate nitrogen‐containing ligands tris(3,5‐dimethylpyrazol‐1‐ylmethyl)amine (L0N4) and tris(3,5‐diisopropylpyrazol‐1‐ylmethyl)amine (L1N4), namely the copper(II) chlorido complexes [Cu^II^(L0N4)Cl~2~] (1) and [Cu^II^(L1N4)Cl~2~] (2), the copper(II) nitrato complexes Cu^II^(L0N4)(NO~3~) (3) and Cu^II^(L1N4)(NO~3~) (4), and the copper(II) sulfato complexes [Cu^II^(L0N4)(SO~4~)] (5) and [Cu^II^(L1N4)(SO~4~)] (6), and the copper(I) complexes Cu^I^(L0N4) (7) and Cu^I^(L0N4)(PPh~3~) (8), have been systematically synthesized in order to investigate the influence of the number of nitrogen donors on their structures, properties, and reactivity. All copper(II) complexes were fully characterized by X‐ray crystallography and by IR/far‐IR, UV/Vis absorption, and ESR spectroscopy. Although the structure of 7 was not determined by X‐ray crystallography, this complex and the structurally characterized copper(I) triphenylphosphane complex 8 were fully characterized by IR/far‐IR and NMR spectroscopy. A comparison of the copper(II) complexes with two tris(pyrazol‐1‐ylmethyl)amine ligands with different bulkiness of the pyrazolyl rings has allowed us to evaluate the second coordination sphere effects of the ligands. Moreover, the structures and physicochemical properties of these complexes are compared with those of related complexes containing the neutral tridentate tris(pyrazolyl)methane ligand and the neutral bidentate bis(pyrazolyl)methane ligand. Finally, the relative stability of the copper(I) complexes is discussed. The influence of the number of nitrogen donors in copper complexes is observed from these systematic results.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)