Synthesis and Structure of Novel RuII-NC-Me Complexes and Their Activity Towards Nitrile Hydrolysis: An Examination of Ligand Effects

MOLA, JOAQUIN; PUJOL, DAVID; RODRÍGUEZ, MONTSERRAT; ROMERO, ISABEL; SALA, XAVIER; KATZ, NÉSTOR; PARELLA, TEODOR; BENET-BUCHHOLZ, JORDI; FONTRODONA, XAVIER; LLOBET, ANTONI

AUSTRALIAN JOURNAL OF CHEMISTRY

CSIRO Publishing

Año: 2009 vol. 62 p. 1675 - 1683

0004-9425

The synthesis and isolation of newRuII–acetonitrile complexes, of general formula trans,fac-[Ru(bpea)(B)(MeCN)](BF4)2 (bpea=N,N-bis(2-pyridylmethyl)ethylamine; B=bpy, 2,2
-bipyridine, 4; B=dppe, 1,2-bis(diphenylphosphino)ethane, 5), together with a synthetic intermediate trans,fac-[Ru(NO3)(bpea)(dppe)](BF4), 6, are described. Ru(bpea)Cl3, 1, is used as the starting material for the synthesis of all complexes 2–6 presented in this paper, which are characterized by analytical, spectroscopic (IR, UV/Vis, 1D and 2D NMR), and electrochemical techniques (cyclic voltammetry). Furthermore, complexes 4, 5, and 6 have also been characterized in the solid state by single crystal X-ray diffraction analysis. Their structures show a distorted octahedral geometry where the bpea ligand binds in a facial mode, the bidentate ligands bpy and dppe bind in a chelate manner, and finally the MeCN or the NO−3 ligand occupy the sixth position of the octahedral Ru metal centre. The kinetics of the basic hydrolysis of the coordinated MeCN ligand for complexes 4 and 5 and for the related complex [Ru(phen)(MeCN)([9]aneS3)](BF4)2, 7, which contains the 1,4,7-trithiacyclonane ligand ([9]aneS3) and 1,10-phenanthroline (phen) is also described. Second-order rate constants for acetonitrile hydrolysis measured at 25◦C of k =1.01×10−3M−1 s−1 for 4, 1.08×10−4M−1 s−1 for 5, and 6.8×10−3M−1 s−1 for 7, have been obtained through UV-vis spectroscopy. Activation parameters have also been determined over the temperature range 25.0–45.0◦C and agree with a mechanism that involves an associative rate-determining step. Finally the electronic and steric influence of the auxiliary ligands on this reaction for the above and related complexes is discussed.