versión impresa ISSN 0366-1644
Bol. Soc. Chil. Quím. v.44 n.4 Concepción dic. 1999
ELECTROCHEMICAL PROPERTIES OF RHENIUM CARBONYL
COMPLEXES CONTAINING TERPYRIDINE LIGAND DERIVATIVES
Departamento de Química Aplicada, Facultad de Química y Biología, Universidad de
Santiago de Chile, Santiago, Chile.
1Laboratoire de Chimie de Coordination et Catalyse, UMR6509, CNRS. Université de Renne
I, Rennes, France.
2Escuela de Química, Facultad de Ciencias, Universidad Central de Venezuela, Caracas,
3Centro de Investigaciones Químicas, Facultad de Ingeniería, Universidd de Carabobo,
(Recibido: Mayo 20, 1999 - Aceptado: Julio 30, 1999)
Correlations between the oxidation potentials and the stretching frequencies of the carbonyl groups in the fac-tricarbonylbromo(polypyridyl)rhenium(I) complexes with respect to the BrRe(CO)5 precursor are discussed.
KEY WORDS: Cyclic voltammetry, ligand effect, rhenium(I) complexes, heterocyclic nitrogen ligands.
Correlaciones entre los potenciales de oxidación y las frecuencias de estiramiento de los grupos carbonilos son discutidas en complejos tricarbonilbromo(polipiridilo) de renio(I), respecto al precursor BrRe(CO)5.
PALABRAS CLAVES: Voltametría cíclica, efecto ligando, complejos de renio(I), ligandos nitrogenados heterocíclicos.
*To whom correspondence should be addressed. Casilla 40-33, Fax: 56-2-6812108, e-mail: firstname.lastname@example.org, Santiago, Chile.
Electrochemical potential measurements are extremely sensible to any variation of the electronic density about the metal center in a transition metal complex. This sensibility can be used to monitoring the electronic effects provided by the replacement of one ligand by another or by the use substituted or unsubstituted ligands on many properties of the complex1). The oxidation potential of the metal (EpOX) in a coordination compound can be related with the electronic density about the metal center or more specifically can be correlated with the changes on the HOMO energies. Several molecular parameters such as vibrational and electronic transitions and even the chemical reactivities can be severely affected by modification of the redox potentials2). In carbonyl complexes the EpOX and the stretching frequencies of the carbonyl groups (nC-O) can be correlated properly by using specific ligands to modificate directly the strength of the p backbonding between the metal and the carbonyl group3).
We report here correlations between the EpOX and the DnC-O obtained from a number of BrRe(CO)3(L) complexes where L is a substituted terpyridine ligand (Figure 1). The heterocyclic nitrogen ligands and the rhenium(I) complexes were prepared by published procedures4). Cyclic voltammetry was performed with a Bank-Wenking POS 73 potentiostat, a Gould OS 4100 oscilloscope and a Graphtec XY recorder WX 4301. The three-electrode configuration contained a platinum button working electrode, platinum wire as auxiliary electrode and saturated calomel electrode (SCE) as reference. 0.1 mol L-1 of tetrabutylammonium perchlorate (TBAP) dry solution, oxygen-free acetonitrile was used as electrolyte. IR spectra were recorded on a Bruker IFS-66V FT spectrometer in KBr disk and CHCl3 solutions.
|FIG. 1. Heterocyclic nitrogen ligands: a) tpy(R=H): ph-tpy (R=ph); py-tpy (R=py); tpy-ph-tpy (R=ph-tpy); b) dq-py (X=CH); dn-py (X=N); c) ph-ddpy (R=ph); py-ddpy (R=py).|
|aredox potential in V vs Fc+/Fc, in CH3CN 0.1 mol L-1 OF TBAP, n=200mVs-1;birreversible; cDEp=Epcprecursor-Epa in mV, where Epc and Epa are cathodic and anodic peak potentials, respectively; d Dnc-o=nco ncocomplex|
Anodic behaviour. All the complexes show two oxidation processes between 0.4 and 1.5 V vs Fc+/Fc range, except for the BrRe(CO)3(py-dppy) complex. The first irreversible one-electron peak should be associated with the oxidation Re(II)/Re(I) pair4). The most positive oxidation peak is difficult to assign to a specific process due to irreversibility of the initial oxidation6).
|FIG. 2. Correlation between EpcOX and DnC-O for the series BrRe(CO)3(L).|
Traditionally the terpyridine ligand coordinates as a tridentate chelate. The compounds studied in this work show an IR spectra where three strong bands in the nC-O stretching region which namely corresponds to the normal vibration modes nC-O of terminal carbonyl groups in molecules with Cs symmetry7). The above implies that the heterocyclic nitrogen ligand acts as an asymmetric bidentate chelate and non as usually terpyridine ligand does. The coordination of the heterocyclic nitrogen ligands increases the backbonding on the carbonyl groups. By comparison of the stretching frequency of the carbonyl groups in the polypyridyl complex with respect to the precursor BrRe(CO)5 complex, DnC-O = nC-Oprecursor - nC-Ocomplex (Table I) we can estimate the distribution excess of negative charge on the carbonyl groups. The movement of this excess of charge provided by the heterocyclic nitrogen ligands on the metal center and distributed on the carbonyl groups can be monitored by analyzing the redox potential. Thus it is possible to establish a correlation between the high frequency (nC-O1) of the carbonyl stretching vibration and the oxidation potential of the ReII/ReI pair. A lineal relation should be found for the studied complexes (Eq. 2):
aredox potential in V vs Fc+/Fc, in CH3CN 0.1 mol L-1 of TBAP, n = 200 mV s-1; birreversible; c DEp = Epc - Epa in mV, where Epc and Epa are cathodic and anodic peak potentials, respectively; d DnC-O = nC-Oprecursor - nC-Ocomplex
However as can be observed in Figure 2 the measurements show several points which are far from a lineal relation slope. A polynomial of high order containing terms derived from EpOX larger than 1 can be rationalized other effects that can appear for high or low potential values (Eq. 3):
DnC-O = A + B (E1/2) + C (E1/2)2 + ...00000000000000000(3)
The above relation allows to estimate or predict the metal oxidation potential from the differences abserved for the DnC-O.
In accordance with the values contained in Table I, the polynomial regression with DnC-O in cm-1 and EpOX,1 in volts (Eq. 4) becomes:
This work was supported by DICYT/USACH, FONDECYT (1980374) and Prorject CNRS/CONICYT (Chile-France). We thank to S. Fernández for his assistance with computer calculations. A.J.P. thanks to CDCH-UCV (AI 4232.98).
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