Repozytorium

Reactivity of bulky tris(phenylpyrazolyl)methanesulfonate copper(I) complexes towards small unsaturated molecules.

Autorzy

Bruno G. M. Rocha

R. Wanke

Silva M. Fátima. C. Guedes da

Konstantin V. Luzyanin

Luisa M. D. R. S. Martins

Piotr Smoleński

Armando J. L. Pombeiro

Rok wydania

2012

Czasopismo

Journal of Organometallic Chemistry

Numer woluminu

714

Strony

47-52

DOI

10.1016/j.jorganchem.2012.03.022

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Reaction of the tris(3-phenylpyrazolyl)methane sulfonate species (TpmsPh)Li with the copper(I) complex [Cu(MeCN)4][PF6] affords [Cu(TpmsPh)(MeCN)] 1. The latter, upon reaction with equimolar amounts of cyclohexyl- (CyNC) or 2,6-dimethylphenyl (XylNC) isocyanides, or excess CO, furnishes the corresponding Cu(I) complexes [Cu(TpmsPh)(CNR)] (R = Cy 2, Xyl 3) or [Cu(TpmsPh)(CO)] 4. The ligated isocyanide in 2 or 3 (or the acetonitrile ligand in 1) is displaced by 3-iminoisoindolin-1-one to afford 5, the first copper(I) complex containing an 3-iminoisoindolin-1-one ligand. The ligated acetonitrile in 1 undergoes nucleophilic attack by methylamine to give the amidine complex [Cu(TpmsPh){MeC(NH)NHMe}] 6, whereas only the starting materials were recovered from the attempted corresponding reactions of 2 and 3 with methylamine. Complexes 1 or 6 form the trinuclear hydroxo-copper(II) species [(μ-Cu){Cu(μ-OH)2(TpmsPh)}2] 7 upon air oxidation in moist methanol. In all the complexes the scorpionate ligand facially caps the metal in the N,N,O-coordination mode.

Słowa kluczowe

Tris(pyrazolyl)methanesulfonate ligand, Copper complexes, Isocyanide, Carbon monoxide, 3-Iminoisoindolin-1-one

Adres publiczny

https://doi.org/10.1016/j.jorganchem.2012.03.022

Strona internetowa wydawcy

http://www.elsevier.com

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