Electrochemical Synthesis and Structural Characterization of a Novel Mixed-valence Copper (i)-copper (ii) Complex: {[bis(ethylenediamine) Copper (ii)] Bis[diiodocuprate (i)]}

A novel, mixed-valent copper(I)-copper(II) complex, {[bis(ethylene-diamine)copper(II)] bis[diiodocuprate(I)]} (1), has been prepared by electrochemical dissolution of a sacrificial copper anode in a solution of ethylenediamine (en), I 2 and tetraethylammoniumperchlorate (TEAP) as supporting electrolyte in acetonitrile (AcN) and characterized by single-crystal X-ray structure determination. The crystal structure of the complex 1 shows that it consists of a CuI 2 polymer formed from I-ligands bridging Cu(I) ions, with a nearly square planar geometry of bivalente Cu(II) atoms chelated by two ethylenediamine ligands. The results also show that direct electrosynthesis of the complex had high current efficiency, purity and electrolysis yield.


Introduction
The design of complex molecular architectures based on transition metal atoms and organic ligands is an important goal for synthetic chemistry as it provides the opportunity to control or encode the properties of a material at the molecular level [1].Suitable organic ligands favoring structure-specific self-assembly are the bases for the construction of coordination architectures.On the other hand, copper halides have been successfully used for the synthesis of uncharged coordination polymer arrays [2][3][4].Various factors, such as the stiochiometric metal-to-ligand ratio, the halide and the nature and substitution of the ligand have been shown to influence the form of the copper-halide motifs and the structures of the resulting coordination polymer [2,3].Recently, increasing attention has been paid to the use of flexible bridging units in the construction of supramolecular architectures [5,6] and this approach is attractive because the flexibility and conformation freedoms of such ligands offer the possibility for the construction of unprecedented frameworks with tailored properties and functions [7].
Although to date remarkable Cu(I) complexes [8][9][10][11] and examples of Cu(I) complexes with halocuprate anion [12][13][14] have been reported, there is no report on diiodocuprate (I) anion polymeric complex with ethylenediamine.Thus, we report herein the electrosynthesis and crystal structure of a novel Cu(I) polymeric complex with potentiostatic dissolution of copper anode in a solution of ethylendiamine and iodine in AcN.

Electrosynthesis
Direct anodic dissolution of copper metal and cathodic reduction of iodine in AcN proved to be a simple and efficient one-step route to new copper(I) iodide ligand polymeric complex, {[Cu(en) 2 ][CuI 2 ] 2 } n (1) in an undivided cell.The dark brown air-stable crystalline complex is obtained by dissolving in DMF.The complex is insoluble in water and most common organic solvents except DMF.The electrochemical cell for this system could be presented as follows: The electron transfer reaction mechanism involves the anodic oxidation of copper to Cu + , which in the presence of I -(resulting from the reduction of I 2 at the cathode) forms the CuI 2 -complex.However, since en is a stronger ligand than I -, some of Cu + participates in a disproportionation reaction to form Cu +2 as Cu (en)

Electrochemistry
A sweep for complex from +0.4 to +1.2 V shows only one quasi-reversible anodic peak (E A1 = 0.98 V) and the backwards cathodic sweep (+1.2 to 0.0 V) shows two cathodic peaks at E C1 = 0.74 V and E C2 = 0.09 V (Figure 1).In a second reversing anodic sweep another anodic peak (E A2 = 0.61 V) corresponding to the reoxidation of the product of cathodic peak at E C2 = 0.09 V appeared.If the studied range is limited from +1.2 to +0.6 V (Figure 1, inset, right) a quasi-reversible wave at E C1 = 0.74 V and E A1 = 0.98 V was observed and assigned to the Cu(II)/Cu(I) redox couple, while a potential sweep in the limited range of +0.8 to 0.0 V shows the second redox couple (E C2 = 0.09 V, E A2 = 0.61 V) corresponding to Cu(I)/Cu(0).The latter redox assignment is further supported by recording the cyclic voltammogram of CuI under the same experimental conditions.As it can be seen from Figure 1 (inset, left) the Cu(I) in CuI cyclic voltammogram is reduced to Cu(0) at E C2 = 0.09 V and its anodic compartment wave is observed at E A2 = 0.61 V, which is a good indication of the presence of a Cu(I)/Cu(0) redox couple in the complex.
Since the cyclic voltammogram of ethylenediamine didn't show any wave in the potential range of 0.0 to 1.2 V (data not shown), thus the redox couples in the complex have been assigned to the metal center in the complex.Therefore, the observed cyclic voltammogram was consistent and characteristic of two Cu (II)/Cu (I) and Cu (I)/Cu (0) redox couples in the structure of the complex.

Structural studies
The crystallographic data are summarized in Table 1 and selected bond distances and angles are given in Table 2. Views of the [Cu (en) 2 ][CuI 2 ] 2 complex 1 shown in Figures 2 and 3 reveal that it crystallized in the monoclinic crystal system with space group C2/m.Complex 1 is mixed-valence.The asymmetric unit of 1 contains two crystallographically independent metal centers in the crystal structure.The bivalent Cu (1) atom has a nearly square planar geometry and was chelated by two ethylenediamine ligands.The two inter and intraligand N-Cu-N angles differ only slightly from 90° (85.51(27)°-94.49(27)°),and the two N-Cu-N angles are close to 180°.The Cu-N distance 2.003(10)Å is similar to those found in other Cu(II) complexes [15][16][17].The structure of 1 consisted of a chain of alternatively perpendicular planes Cu 4 I 4 running along the c axis of CuI 2 -formed from I - ligands bridging Cu (I) ions.The monovalent Cu(2) atom ion in this complex is distorted tetrahedral.The I1 i -Cu2-I1 angle is much less than 109.5°,being only 96.72(0)°.On the contrary, the I2-Cu2-I1 angle (112.25(0)°,) is much larger than those of a tetrahedral complex.The average Cu-I bond distance (2.6752 Å) is similar to that found in other Cu (I) (diimine) pseudotetrahedral complexes [18][19][20].Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters are reported in Table 3.   Largest difference Peak and hole (e.Å -3 ) 0.799 and -0.740

Conclusions
The utility of direct and uncomplicated electrosynthesis to obtain this type of copper complex of ethylenediamine with high yield and high purity has been demonstrated.Comparing with the usual chemically copper complexes of ethylenediamine prepared over the years [21], the resulting complex is a new and unusual member of an interesting class of mixed-valence one-dimensional supramolecular copper complexes.

Apparatus
Electrochemical experiments were performed using a Metrohm model 746 VA trace analyzer connected a 747 VA stand.A glassy carbon electrode (0.2 mm diameter) was used as the working electrode.A platinum wire and a commercial KCl saturated Ag/AgCl electrode from Metrohm were used as the auxiliary and reference electrodes, respectively.The solutions were purged with 99.999% argon for 10 min before the start of the experiments.Electrosynthesis was performed using a Zahner electrik PP200 potentiostat/galvanostat.The electrochemical cell consists of a tall-form beaker (100 mL) with three cross sectional openings.The potential of copper anode was held 0.5 V with respect to an Ag/AgCl reference electrode and a platinum sheet was used as a cathode counter electrode.A magnet stirring system was also used.

Electrosynthesis
Electrosynthesis was carried out in an undivided cell.The copper anode and platinum cathode were inserted in a solution of ethylenediamine (0.030 g, 0.5 mmol), iodine (0.126 g, 0.5 mmol) and 0.10 M TBAP as supporting electrolyte in can (50 mL).Potentiostatic oxidation of the copper anode at 0.5 V resulting in colorless solution initially.Electrolysis was stopped after 30 minutes and brown product was filtered off, washed with AcN and dried.The final brown precipitate was dissolved in DMF and allowed to stand over several days to deposit the complex as dark brown prisms suitable for X-ray crystallography.The IR spectra of both, brown precipitate and its crystalline complex showed the same bands, indicating that DMF did not engaged in the resulted crystalline complex.

Figure 1 .
Figure 1.Cyclic voltammogram of 1 at the glassy carbon electrode in DMF.Initial anodic scan from 0.6 V to 1.2 V and reversing scan up to 0.0 V. Inset right: cyclic voltammogram of 1 in the 1.2 V to 0.6 V range.Inset left: cyclic voltammogram of CuI in the 0.8 V to 0.0 V range.Scan rate 50 mVs -1 .

Figure 2 .
Figure 2. ORTEP view of the crystal structure of [Cu(C) 2 ] + , showing the atom labeling scheme.The thermal ellipsoids enclose 50% of the electronic density.

Figure 3 .
Figure 3.A view of the overall network slightly offset from directly down the c axis.

Table 1 .
Crystal data and structure refinement for 1.