About this Journal Submit a Manuscript Table of Contents
Bioinorganic Chemistry and Applications
Volume 2010 (2010), Article ID 960571, 9 pages
http://dx.doi.org/10.1155/2010/960571
Research Article

Mononuclear and Dinuclear Manganese(II) Complexes from the Use of Methyl(2-pyridyl)ketone Oxime

1Department of Chemistry, University of Patras, 265 04 Patras, Greece
2Department of Chemistry, University of Florida, Gainesville, FL 32611-7200, USA
3Institute of Materials Science, National Centre of Scientific Research “Demokritos”, 153 10 Aghia Paraskevi Attikis, Greece
4Department of Chemistry, University of Cyprus, 1678 Nicosia, Cyprus

Received 23 March 2010; Accepted 3 May 2010

Academic Editor: Evy Manessi-Zoupa

Copyright © 2010 Constantinos G. Efthymiou et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The reactions of methyl(2-pyridyl)ketone oxime, (py)C(Me)NOH, with manganese(II) sulfate monohydrate have been investigated. The reaction between equimolar quantities of M n S O 4 H 2 O and (py)C(Me)NOH in H 2 O lead to the dinuclear complex [ M n 2 ( S O 4 ) 2 { ( p y ) C ( M e ) N O H } 4 ] ( p y ) C ( M e ) N O H , 𝟏 ( p y ) C ( M e ) N O H , while employment of NaOMe as base affords the compound [ M n ( H C O 2 ) 2 { ( p y ) C ( M e ) N O H } 2 ] (2). The structures of both compounds have been determined by single crystal X-ray diffraction. In both complexes, the organic ligand chelates through its nitrogen atoms. The IR data are discussed in terms of the nature of bonding and the structures of the two complexes.

1. Introduction

There is currently a renewed interest in the coordination chemistry of oximes [1]. The research efforts are driven by a number of considerations. One of these is that they are considered to be reasonable models for the biologically significant imidazole donor group of the amino acid histidine [2]. Thus, they potentially can be used for the synthesis of various nuclearity metal clusters to model M x sites in biomolecules, including elucidating the structure and mechanism of action of the C a M n 4 core of the water oxidizing complex within the photosynthetic apparatus of green plants and cyanobacteria [3, 4]. In addition, metal complexes of oximes can be used in several other applications, that is, the solution of pure chemical problems [5, 6], the development of new oxygen activation catalysts based on nickel(II) polyoximate complexes [7] and the application of metal ion/oxime systems as efficient catalysts for the hydrolysis of organonitriles [8]. In the latter, metal ions can behave as extremely strong activators of RCN molecules towards nucleophilic attack by O H / H 2 O . Other applications of metal complexes of oximes include the design of C a 2 + - and B a 2 + -selective receptors based on site-selective transmetallation of polynuclear zinc (II)/polyoxime complexes [9], the study of metal-ion assisted organic transformations [10], and the mechanistic investigation of corrosion inhibition by Acorga P5000 (a modern corrosion inhibitor comprising 5-nonylsalicylaldoxime as a mixture of carbon-chain isomers) on iron surfaces [11]. Note also that oximate ligands are employed in the synthesis of homo- and heterometallic [1, 12] clusters and coordination polymers [13] with interesting magnetic properties, including single-molecule magnetism [1416], and single-chain magnetism [17] behavior.

Ligands containing one oxime group and one pyridyl group, without other donor sites, are popular in coordination chemistry. Metal-free pyridine oximes exhibit a plethora of biological properties including action on the cardiovascular system, sedative, antidepressant, antispasmodic, cytotoxic, antiviral, and bactericidal activities, while they are good antidotes for poisoning by organophosphorus compounds [18]. Most of these ligands contain a 2-pyridyl group, and thus are named 2-pyridyl oximes, (py)C(R)NOH (Scheme 1). The anionic forms of these molecules, (py)C(R)NO , are versatile ligands for a variety of research objectives, including 𝜇 2 and 𝜇 3 behaviour; the activation of 2-pyridyl oximes by 3d-metal centers towards further reactions is also becoming a fruitful area of research. The majority of the metal complexes of these ligands have been prepared in the last 15 years and much of their chemistry remains to be explored in more detail [1].

960571.sch.001
Scheme 1: General structural formula and abbreviations of simple 2-pyridyl oximes, including methyl(2-pyridyl)ketone oxime [(py)C(Me)NOH].

With only few exceptions [19, 20], the hitherto structurally characterized metal complexes containing neutral 2-pyridyl oximes as ligands are mononuclear. The donor atoms of the neutral 2-pyridyl oximes in metal complexes are the nitrogen atom of the oxime group and the nitrogen atom of the pyridyl group. Thus, (py)C(R)NOH behave as 𝑁 , 𝑁 -chelating ligands (see Scheme 2) making necessary the employment of additional inorganic or organic anions to complete the coordination sphere of the metal centre or to balance the charge of the complex cation. A variety of monoanions have been used for this reason, for example, P h C O 2 [21], C l [22, 23], B r [24], and N O 3 [25]. Recently, we have started a research program to explore the use of the sulfate ion, S O 4 2 , in 3d-metal/2-pyridyl oxime chemistry, instead of the abovementioned monoanionic ligands. The possible advantages of using S O 4 2 include (i) the possibility of triggering aggregation of preformed smaller species into new products, and (ii) the possible diversion of known reaction systems developed using inorganic monoanions to new species as a result of the higher charge and higher denticity of the sulfate ligand.

960571.sch.002
Scheme 2: The common coordination mode of the neutral 2-pyridyl oximes and the Harris notation [26] which describes this mode.

The sulfate ion [27] is currently a ligand of intense interest. The 𝜇 2 , 𝜇 3 , 𝜇 4 , 𝜇 5 , 𝜇 8 , or 𝜇 1 0 potential of S O 4 2 (Scheme 3) prompted as to combine 2-pyridyloximes with the sulfate ligand to aim at new types of compounds.

960571.sch.003
Scheme 3: The up to now crystallographically established coordination modes of the sulfato ligand and the Harris notation [26] which describes these modes.

In this paper, we report the synthesis and the X-ray structural characterization of the two new Mn(II) complexes [Mn2(SO4) 2 { (py)C(Me)NOH } 4] (py)C(Me)NOH (1 (py)C(Me)NOH) and [ Mn(HCO2)2 { (py)C(Me)NOH } 2] (2) which contain the neutral methyl(2-pyridyl)ketone oxime as organic ligand. The IR data are discussed in terms of the nature of bonding and the structures of the two complexes.

2. Experiments

All manipulations were performed under aerobic conditions using materials and solvents as received. IR spectra were recorded on a Perkin-Elmer PC16 FT-IR spectrometer with samples prepared as KBr pellets.

[Mn2 (SO4)2 { (py)C(Me)NOH } 4 ] (py)C(Me)NOH (1 (py)C(Me)NOH)
Solid MnSO 4 H 2 O (0.067 g, 0.40 mmol) was added to a slurry of (py)C(Me)NOH (0.054 g, 0.40 mmol) in H 2 O ( 1 5 c m 3 ); the solid soon dissolved and the solution was stirred for 1 hour at room temperature. The resultant solution was left for slow evaporation. After one week, yellow crystals appeared which were collected by filtration, washed with cold H 2 O ( 1 c m 3 ), cold MeOH ( 1 c m 3 ) and ice-cold E t 2 O ( 2 c m 3 ), and dried in air. The yield was 79% (based on the metal). Found %: C, 42.94; H, 3.89; N, 14.51. Calc % for C 3 5 H 4 0 O 1 3 N 1 0 S 2 M n 2 : C, 42.78; H, 4.10; and N, 14.25. Selected IR data (KBr, c m 1 ): 3420 (wb), 3150 (m), 3069 (m), 2843 (m), 2363 (w), 2343 (w), 1654 (w), 1593 (s), 1561 (m), 1476 (s), 1437 (m), 1327 (m), 1285 (w), 1215 (m), 1124 (s), 1080 (s), 1030 (s), 1010 (s), 989 (s), 781 (s), 748 (m), 683 (m), 631 (m), 592 (m), 561 (w), 494 (w), 452 (w), and 447 (w).

[Mn(HCO2 )2 {(py)C(Me)NOH}2 ](2)
Solid NaOMe (0.090 g, 1.50 mmol) was added to a colourless solution of (py)C(Me)NOH (0.204 g, 1.50 mmol) in C H 2 C l 2 ( 2 0 c m 3 ); the solid soon dissolved. Solid MnSO 4 H 2 O (0.250 g, 1.50 mmol) was then added and the resulting solution was stirred for 24 hours at room temperature. A small quantity of undissolved material was removed by filtration and the dark brown filtrate layered with E t 2 O (40  c m 3 ). Slow mixing gave X-ray quality yellow crystals of the product. The crystals were collected by filtration, washed with cold H 2 O (1  c m 3 ), cold MeOH (2  c m 3 ), and ice-cold E t 2 O ( 2 × 3 c m 3 ), and dried in air. The yield was 45% (based on the metal). Found %: C, 46.95; H, 4.26; N, 13.43. Calc % for C 1 6 H 1 8 O 6 N 4 M n : C, 46.82; H, 4.13; N, 13.98. Selected IR data (KBr, c m 1 ): 3412 (mb), 3073 (w), 2362 (m), 1846 (m), 1597 (s), 1562 (s), 1475 (s), 1436 (m), 1365 (s), 1348 (s), 1326 (m), 1250 (w), 1165 (w), 1137 (m), 1042 (s), 961 (m), 782 (s), 751 (s), 683 (m), 562 (w), and 458 (w).

2.1. X-Ray Crystallography

For 1 (py)C(Me)NOH, X-Ray data were collected at 298 K using a Crystal Logic Dual Goniometer diffractometer with graphite-monochromated M o - 𝐾 𝑎 radiation ( 𝜆 = 0 . 7 1 0 7 3 Å). Lorentz, polarization, and Ψ -scan absorption corrections were applied using Crystal Logic software. Symmetry equivalent data were averaged with 𝑅 i n t = 0.0084, to give 3727 independent reflections from a total 3964 collected. The structure was solved by direct methods and refined by full-matrix least-squares on F 2 , using 3727 reflections and refining 325 parameters. All nonhydrogen atoms were refined anisotropically. Hydrogen atoms were either located by difference maps and were refined isotropically or were introduced at calculated positions as riding on bonded atoms.

For 2, X-ray data were collected at 100 K using a Oxford Diffraction diffractometer with graphite-monochromated M o - 𝐾 𝑎 radiation ( 𝜆 = 0 . 7 1 0 7 3  Å). Symmetry equivalent data were averaged with 𝑅 i n t = 0 . 0 1 6 0 , to give 9343 independent reflections from a total of 13039 collected. The structure was solved by direct methods and refined by full-matrix least-squares on F 2 , using 9343 reflections and refining 258 parameters. All non-hydrogen atoms were refined anisotropically. Hydrogen atoms were either located by difference maps and were refined isotropically or were introduced at calculated positions as riding on bonded atoms.

Details of the data collection and refinement for 1 (py)C(Me)NOH and 2 are given in Table 1.

tab1
Table 1: Crystal data and structure refinement for 1 (py)C(Me)NOH and 2.

3. Results and Discussion

3.1. Synthetic Comments

Treatment of MnSO4 H2O with one equivalent of (py)C(Me)NOH in H 2 O gave a colorless solution from which the new dinuclear compound [Mn2 (SO4 )2 { (py)C(Me)NOH } 4 ] (py)C(Me)NOH (1 (py)C(Me)NOH) was obtained in 80% yield. Its formation can be summarized in (1). 2 M n S O 4 H 2 O + 5 ( p y ) C ( M e ) N O H H 2 O M n 2 S O 4 2 { ( p y ) C ( M e ) N O H } 4 ( p y ) C ( M e ) N O H + 2 H 2 O 𝟏 ( p y ) C ( M e ) N O H . ( 1 ) The nonstoichiometric MnSO4 H2O to (py)C(Me)NOH reaction ratio (1 : 1) employed for the preparation of 1 (py)C(Me)NOH (Section 2) did not prove detrimental to the formation of the complex. With the identity of 1 (py)C(Me)NOH established by single-crystal X-ray crystallography, the “correct” stoichiometry (1 : 2.5) was employed and led to the pure compound in high yield.

As a next step, we decided to add base in the reaction mixture targeting the deprotonation of the organic ligand. Thus, treatment of MnSO4 H2O with one equivalent of (py)C(Me)NOH and one equivalent of NaOMe in C H 2 C l 2 gave a dark brown solution from which the mononuclear compound [ M n ( H C O 2 ) 2 { ( p y ) C ( M e ) N O H } 2 ] (2) was obtained. Its formation can be summarized in(2) M n S O 4 H 2 O + 2 ( p y ) C ( M e ) N O H + 2 N a O M e + 2 O 2 C H 2 C l 2 M n H C O 2 2 { ( p y ) C ( M e ) N O H } 2 + N a 2 S O 4 + 3 H 2 O . ( 2 )

To our surprise, an amount of the methoxide ions did not act as proton acceptors but they got oxidized to formates ( H C O 2 ) during the aerial aggregation process [28]. Thus, the organic ligand in 2 is neutral. As expected, the nature of the base is crucial for the identity of the product; employment of N E t 3 , N M e 4 OH, N E t 4 O H , LiOH H2O etc. leads to dark brown oily materials that have not been characterized. Also, note that: (i) The color of 2 (yellow) is different than the color of the reaction mixture (dark brown, this colour is characteristic of M n I I I or M n I I / I I I species), and (ii) a similar reaction, but with (py)C(ph)NOH instead of (py)C(Me)NOH, yields the octanuclear mixed-valent cluster [ M n I I 4 M n I I I 4 O 4 ( N O 3 ) 2 { ( p y ) C ( p h ) N O } 8 (HCOO)2 (MeOH)2 ] [29] whose core consists of two butterfly subunits. These observations indicate that compound 2 is not the only product of the reaction and that, presumably, a higher nuclearity cluster, with the metals at higher oxidation states, is present in solution. Work is in progress to isolate the second product from the reaction mixture.

3.2. Description of Structures

Selected interatomic distances and angles for complexes 1 (py)C(Me)NOH and 2 are listed in Tables 2 and 4, respectively. The molecular structures of the two compounds are shown in Figures 1 and 2.

tab2
Table 2: Selected dond lengths (Å) and angles ( ) for 1 (py)C(Me) 𝑁 𝑂 𝐻 . 𝑎
960571.fig.001
Figure 1: The dinuclear molecule present in 1 (py)C(Me)NOH. Primes are used for the symmetry-related atoms.
960571.fig.002
Figure 2: The molecular structure of compound 2.

Complex 1 (py)C(Me)NOH crystallizes in the triclinic space group 𝑃 - 1 . Its structure consists of dinuclear [ M n 2 ( S O 4 ) 2 { ( p y ) C ( M e ) N O H } 4 ] molecules and (py)C(Me)NOH molecules in the crystal lattice. The dinuclear molecules lie on a crystallographic inversion center. The two M n I I atoms are bridged by two 𝜂 1 : 𝜂 1 :  𝜇 2 or 2.1100 (Harris notation [26]) sulfato ligands; two N,N -chelating (py)C(Me)NOH ligands complete six coordination at each metal center. The ligating atoms of (py)C(Me)NOH are the nitrogen atoms of the neutral oxime and 2-pyridyl groups. Thus, adopting the Harris notation, (py)C(Me)NOH behaves as an 1.011 ligand.

The coordination sphere of the M n I I ion in 1 (py)C(Me)NOH exhibits a slightly distorted octahedral geometry as a consequence of the relatively small bite angles of the chelating ligands [N1–Mn–N2=70.11(10), N11–Mn–N12=70.19(10) ]. Both sulfato oxygen atoms O(31) and O( 3 2 ) are trans to the pyridyl nitrogen atoms N( 1 ) and N( 1 1 ), respectively. Each metal center adopts the cis-cis-trans configuration considering the position of the coordinated S O 4 2 oxygen, pyridyl nitrogen and oxime nitrogen atoms, respectively. The cis arrangement of the oxime groups seems unfavourable, probably due to the steric hindrance arising from the methyl group upon oxime coordination. The long M n M n distance [5.040( 2 ) Å] is a consequence of the presence of the two syn, anti sulfato bridges.

The molecular structure of 1 (py)C(Me)NOH is stabilized by intramolecular hydrogen bonds (Table 3). Each coordinated (py)C(Me)NOH oxime group is strongly hydrogen bonded to an uncoordinated O atom of the sulfato ligand (O33 or O 3 3 ). Thus, O33 (and its symmetry equivalent) participates in two hydrogen bonds.

tab3
Table 3: Dimensions of the hydrogen bonds in complex 1 (py)C(Me) 𝑁 𝑂 𝐻 . 𝑎
tab4
Table 4: Selected dond lengths (Å) and angles ( ) for 2.

Complex 2 crystallizes in the monoclinic space group P 2 1 / n and its structure consists of mononuclear [ M n ( H C O 2 ) 2 { ( p y ) C ( M e ) N O H } 2 ] molecules. Two bidentate chelating (py)C(Me)NOH molecules (1.011 [26], see Scheme 2) and two monodentate H C O 2 ions create six-coordination at the M n I I ion. The coordination geometry of the metal ion is distorted octahedral. As 1 (py)C(Me)NOH, complex 2 is the cis-cis-trans isomer considering the positions of the coordinated H C O 2 oxygen, pyridyl nitrogen and oxime nitrogen atoms, respectively.

Intramolecular hydrogen bonds are present in the structure of 2 (Table 5). The oximic oxygen atom of each (py)C(Me)NOH ligand is very strongly intramolecularly hydrogen bonded to one uncoordinated formate oxygen atom.

tab5
Table 5: Dimensions of the hydrogen bonds in complex 2 . 𝑎

Complexes 1 (py)C(Me)NOH and 2 join a small but growing family of structurally characterized metal complexes containing the neutral or anionic forms of methyl(2-pyridyl)ketone oxime as ligands. The 1.011 ligation mode is the exclusive one for the metal complexes containing the neutral ligand [22, 24, 30].

The structurally characterized Mn complexes of (py)C(Me)NOH and/or ( p y ) C ( M e ) N O [14, 3133] are collected in Table 6, together with the cores of the polynuclear complexes and the ligands’ coordination modes for convenient comparison. Closer inspection of Table 6 reveals that compound 1 is the first member of this subfamily in which the M n I I ions are linked by the S O 4 2 ion. Complex 2 can be compared with the compound [ M n I I ( O 2 C P h ) 2 { ( p y ) C ( M e ) N O H } 2 ] [33] which contains terminal P h C O 2 ions, instead of H C O 2 in 2; the H C O 2 versus P h C O 2 change has little structural effect.

tab6
Table 6: Formulae, coordination modes of the ligands, and cores of the structurally characterized Mn complexes of (py)C(Me)NOH and/or (py)C(Me)NO .
3.3. IR Spectra

Complexes 1 and 2 exhibit medium to strong intensity IR bands at 3400  c m 1 , assignable to 𝜈 (ΟH) vibrations of the (py)C(Me)NOH molecules. The broadness and relatively low frequency of these bands are both indicative of hydrogen bonding.

The ν(C=N) o x i m e and 𝜈 ( N - O ) o x i m e vibrations for the free ligand appear as medium intensity bands at 1566 and 1116  c m 1 , respectively [34, 35]. The 1116  c m 1 band is shifted to a lower wavenumber in 1 and 2 (1, 1080; 2, 1042  c m 1 ). This shift is attributed to the coordination of the neutral oxime nitrogen [22]. The strong band at 1124  c m 1 in the spectrum of 1 (py)C(Me)NOH should also have a 𝜈 ( N - O ) o x i m e character resulting from the presence of lattice (py)C(Me)NOH molecules in the structure. Several bonds appear in the 1 6 5 5 - 1 4 0 0 c m 1 region for both complexes; contribution from the ν(C=N) o x i m e and 𝛿 ( O H ) modes ( > 1580  c m 1 ) are expected in this region, but overlap with the stretching vibrations of the aromatic rings and the carboxylate groups (for 2) renders assignments and discussion of the coordination shifts difficult.

The in-plane deformation band of the 2-pyridyl ring of free (py)C(Me)NOH at 637  c m 1 shifts upwards in 1 (683  c m 1 ) and 2 (683  c m 1 ), confirming the involvement of the ring-N atom in coordination [36]. The appearance of a medium intensity band at 631  c m 1 in the spectrum of 1 (py)C(Me)NOH is indicative of the presence of lattice (py)C(Me)NOH molecules in this complex.

The IR spectrum of the free, that is, ionic, sulfate (the S O 4 2 ion belongs to the 𝑇 d point group) consists of two bands at 1105 and 615  c m 1 , assigned to the 𝜈 3 ( 𝐹 2 ) stretching [ 𝜈 d ( S O ) ] and 𝜈 4 ( 𝐹 2 ) bending [δd (OSO)] modes, respectively [27, 37, 38]. The 𝜈 1 ( 𝐴 1 ) stretching [ 𝜈 𝑠 ( S O ) ] and 𝜈 2 ( 𝐸 ) bending [ 𝛿 d ( O S O ) ] modes are not IR-active (these are Raman-active). The coordination of S O 4 2 to metal ions decreases the symmetry of the group and the 𝜈 3 and 𝜈 4 modes are split [27, 37, 38]. In the case, the S O 4 2 -site symmetry is lowered from 𝑇 d to 𝐶 3 v (monodentate coordination), both 𝜈 1 and 𝜈 2 appear in the IR spectrum with weak to medium intensity, while 𝜈 3 and 𝜈 4 each splits into two bands in both IR and Raman spectra [37]. When the S O 4 2 -site symmetry is lowered from 𝑇 d to 𝐶 2 v (bidentate chelating or bridging coordination), again 𝜈 1 and 𝜈 2 appear in the IR spectrum ( 𝜈 2 splits into two Raman modes), while 𝜈 3 and 𝜈 4 each splits into three IR-active and Raman-active vibrations [37]. The crystallographically established symmetry of the sulfato groups in 1 (py)C(Me)NOH is 𝐶 2 v . The bands at 1215, 1124 and 1080 (overlapping with the N - O o x i m e stretch) c m 1 are attributed to the 𝜈 3 modes [37, 39], while the bands at 592, 631 and 683  c m 1 (the latter two overlapping with the in-plane 2-pyridyl deformations) are assigned to the 𝜈 4 modes [37, 38]. The band at 1010  c m 1 and the two weak features at 494 and 452  c m 1 can be assigned to the 𝜈 1 and 𝜈 2 modes, respectively. The appearance of two 𝜈 2 bands is consistent with a symmetry at the sulfato groups lower than 𝐶 2 v [37, 39]. Thus, from the vibrational spectroscopy viewpoint, the sulfato ligands of 1 (py)C(Me)NOH appear to have 𝐶 i symmetry (and not 𝐶 2 v as deduced from their bidentate character). When the S O 4 2 -site symmetry is lowered from 𝑇 d to 𝐶 i , 𝜈 3 and 𝜈 4 each splits into three IR-active vibrations, 𝜈 2 splits into two ones, while 𝜈 1 appears as a single band [37, 39]. This spectroscopic feature in 1 (py)C(Me)NOH is attributed to the fact that one uncoordinated oxygen atom of each bidentate bridging sulfate is hydrogen bonded to the oxygen atoms of the neutral oxime groups (see Table 3) resulting in a further lowering of the sulphate symmetry [39].

The ν(CO2) bands are difficult to assign in the spectrum of 2 due to the appearance of various stretching vibrations in the 1 6 0 0 - 1 4 0 0 c m 1 region and thus the application of the spectroscopic criterion of Deacon and Phillips [40] is very difficult.

4. Conclusions

The use of the sulfate ligand in combination with neutral (py)C(Me)NOH in Mn(II) chemistry has provided access to the two new neutral complexes [Mn2 (SO4)2 { (py)C(Me)NOH } 4 ] (py)C(Me)NOH (1 (py)C(Me)NOH) and [ M n ( H C O 2 ) 2 { ( p y ) C ( M e ) N O H } 2 ] (2), the latter being sulphate-free. In both complexes, the organic ligand chelates through its nitrogen atoms. The sulfate anion bridges the two M n I I atoms in 1. Compounds 𝟏 ( p y ) C ( M e ) N O H and 2 join a small family of structurally characterized manganese complexes containing the neutral or anionic forms of methyl(2-pyridyl)ketone oxime as ligands, while they are new examples of structurally characterized compounds in which (py)C(Me)NOH exists exclusively in its neutral form.

Analogues of 1 (py)C(Me)NOH and 2 with phenyl(2-pyridyl)ketone oxime, (py)C(ph)NOH, are not known to date, and it is currently not evident whether the stability of these species is dependent on the particular nature of the 2-pyridyl oxime ligand. We are studying this matter. Synthetic efforts are also in progress to “activate” the 𝜇 3 to 𝜇 6 bridging potential of the sulfate ligand in Mn complexes containing 2-pyridyl oximes and/or their anions as a means to get access to clusters and polymers with interesting structural and magnetic properties. Studies on the biological activity of 1 (py)C(Me)NOH and 2 are also planned.

5. Supplementary Information

CCDC 757892 and 757893 contain the supplementary crystallographic data for 1 (py)C(Me)NOH and 2. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html, or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44)1223-336033; or e-mail: deposit@ccdc.cam.ac.uk.

Acknowledgments

This work was supported by the Cyprus Research Promotion Foundation (Grant DIETHNIS/STOXOS/0308/14). In dedication to Professor Nick Hadjiliadis for his retirement and for his important contributions to Bioinorganic Chemistry.

References

  1. C. J. Milios, T. C. Stamatatos, and S. P. Perlepes, “The coordination chemistry of pyridyl oximes,” Polyhedron, vol. 25, no. 1, pp. 134–194, 2006. View at Publisher · View at Google Scholar · View at Scopus
  2. D. T. Rosa, J. A. Krause Baue, and M. J. Baldwin, “Structural and spectroscopic studies of the versatile coordination chemistry of the chiral ligand N,N-bis(1-propan-2-onyl oxime)-L-methionine N-methylamide with NiII and ZnII,” Inorganic Chemistry, vol. 40, no. 7, pp. 1606–1613, 2001. View at Publisher · View at Google Scholar · View at Scopus
  3. K. Sauer, J. Yano, and V. K. Yachandra, “X-ray spectroscopy of the photosynthetic oxygen-evolving complex,” Coordination Chemistry Reviews, vol. 252, no. 3-4, pp. 318–335, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  4. A. Mishra, J. Yano, Y. Pushkar, V. K. Yachandra, K. A. Abboud, and G. Christou, “Heteronuclear Mn-Ca/Sr complexes, and Ca/Sr EXAFS spectral comparisons with the Oxygen-Evolving Complex of Photosystem II,” Chemical Communications, no. 15, pp. 1538–1540, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  5. D. Burdinski, F. Birkelbach, and F. Birkelbach, “Encapsulation by a chromium(III)-containing bicyclic ligand cage. synthesis, structures, and physical properties of heterometal complexes CrIIIMCrIII [M=(H+)2,Li(I),Mg(II),Cu(II), Ni(II),Ni(IV),Co(III),Fe(II),Fe(III),Mn(II)],” Inorganic Chemistry, vol. 37, no. 5, pp. 1009–1020, 1998. View at Scopus
  6. V. Yu. Kukushkin and A. J. L. Pombeiro, “Oxime and oximate metal complexes: unconventional synthesis and reactivity,” Coordination Chemistry Reviews, vol. 181, no. 1, pp. 147–175, 1999. View at Scopus
  7. M. J. Goldcamp, S. E. Robison, J. A. Krause Bauer, and M. J. Baldwin, “Oxygen reactivity of a nickel(II)-polyoximate complex,” Inorganic Chemistry, vol. 41, no. 9, pp. 2307–2309, 2002. View at Publisher · View at Google Scholar · View at Scopus
  8. M. N. Kopylovich, V. Yu. Kukushkin, M. Haukka, J. J. R. Fraústo da Silva, and A. J. L. Pombeiro, “Zinc(II)/ketoxime system as a simple and efficient catalyst for hydrolysis of organonitriles,” Inorganic Chemistry, vol. 41, no. 18, pp. 4798–4804, 2002. View at Publisher · View at Google Scholar · View at Scopus
  9. S. Akine, T. Taniguchi, T. Saiki, and T. Nabeshima, “Ca2+- and Ba2+-selective receptors based on site-selective transmetalation of multinuclear polyoxime-zinc(II) complexes,” Journal of the American Chemical Society, vol. 127, no. 2, pp. 540–541, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  10. A. J. L. Pombeiro and V. Yu. Kukushkin, “Reactivity of coordinated oximes,” in Comprehensive Coordination Chemistry II, J. A. McCleverty and T. J. Meyer, Eds., vol. 1, pp. 631–637, Elsevier, Amsterdam, The Netherlands, 2004.
  11. J. M. Thorpe, R. L. Beddoes, D. Collison, C. D. Garner, M. Helliwell, J. M. Holmes, and P. A. Tasker, “Surface coordination chemistry: corrosion inhibition by tetranuclear cluster formation of iron with salicylaldoxime,” Angewandte Chemie: International Edition, vol. 38, no. 8, pp. 1119–1121, 1999. View at Scopus
  12. S. Khanra, T. Weyhermüller, E. Bill, and P. Chaudhuri, “Deliberate synthesis for magnetostructural study of linear tetranuclear complexes BIIIMnIIMnIIBIII, MnIIIMnIIMnIIMnIII,MnIVMnIIMnIIMnIV, FeIIIMnIIMnIIFeIIICrIIIMnIIMnIICrIII. Influence of terminal ions on the exchange coupling,” Inorganic Chemistry, vol. 45, no. 15, pp. 5911–5923, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  13. D. Robertson, J. F. Cannon, and N. Gerasimchuk, “Double-stranded metal-organic networks for one-dimensional mixed valence coordination polymers,” Inorganic Chemistry, vol. 44, no. 23, pp. 8326–8342, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  14. T. C. Stamatatos, D. Foguet-Albiol, and D. Foguet-Albiol, “Initial example of a triangular single-molecule magnet from ligand-induced structural distortion of a [MnIII3O]7+  complex,” Journal of the American Chemical Society, vol. 127, no. 44, pp. 15380–15381, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  15. C. J. Milios, C. P. Raptopoulou, A. Terzis, F. Lloret, R. Vicente, S. P. Perlepes, and A. Escuer, “Hexanuclear manganese(III) single-molecule magnets,” Angewandte Chemie: International Edition, vol. 43, no. 2, pp. 210–212, 2003. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  16. C. J. Milios, A. Vinslava, and A. Vinslava, “Microwave-assisted synthesis of a hexanuclear MnIII single-molecule magnet,” Inorganic Chemistry, vol. 45, no. 14, pp. 5272–5274, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  17. H. Miyasaka, R. Clérac, K. Mizushima, K.-I. Sugiura, M. Yamashita, W. Wernsdorfer, and C. Coulon, “[Mn2(saltmen)2Ni(pao)2(L)2](A)2 with L = pyridine, 4-picoline, 4-tert-butylpyridine, N-methylimidazole and A=ClO4,BF4,PF6,ReO4: a family of single-chain magnets,” Inorganic Chemistry, vol. 42, no. 25, pp. 8203–8213, 2003. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  18. E. Abele, R. Abele, and E. Lukevics, “Pyridine oximes: synthesis, reactions, and biological activity,” Chemistry of Heterocyclic Compounds, vol. 39, no. 7, pp. 825–865, 2003. View at Publisher · View at Google Scholar · View at Scopus
  19. M. Alexiou, I. Tsivikas, and I. Tsivikas, “High nuclearity nickel compounds with three, four or five metal atoms showing antibacterial activity,” Journal of Inorganic Biochemistry, vol. 93, no. 3-4, pp. 256–264, 2003. View at Publisher · View at Google Scholar · View at Scopus
  20. C. Papatriantafyllopoulou, G. E. Kostakis, C. P. Raptopoulou, A. Terzis, S. P. Perlepes, and J. C. Plakatouras, “Investigation of the MSO4·xH2O(M=Zn,x=7;M=Cd,x=8/3)/methyl 2-pyridyl ketone oxime reaction systemml: a novel Cd(II) coordination polymer versus mononuclear and dinuclear Zn(II) complexes,” Inorganica Chimica Acta, vol. 362, no. 7, pp. 2361–2370, 2009. View at Publisher · View at Google Scholar · View at Scopus
  21. C. J. Milios, P. Kyritsis, C. P. Raptopoulou, A. Terzis, R. Vicente, A. Escuer, and S. P. Perlepes, “Di-2-pyridyl ketone oxime [(py)2CNOH] in manganese carboxylate chemistry: mononuclear, dinuclear and tetranuclear complexes, and partial transformation of (py)2CNOH to the gem-diolate(2−) derivative of di-2-pyridyl ketone leading to the formation of NO3,” Dalton Transactions, no. 3, pp. 501–511, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  22. C. Papatriantafyllopoulou, C. P. Raptopoulou, A. Terzis, E. Manessi-Zoupa, and S. P. Perlepes, “Investigation of the zinc chloride/methyl(2-pyridyl)ketone oxime reaction systemml: a mononuclear complex and an inverse 12-metallacrown-4 cluster,” Zeitschrift für Naturforschung, vol. 61, no. 1, pp. 37–46, 2006. View at Scopus
  23. M. Alexiou, C. Dendrinou-Samara, C. P. Raptopoulou, A. Terzis, and D. P. Kessissoglou, “From monomer zinc-oxamato complexes to tetranuclear inverse 12-membered and octanuclear 12-membered metallacrowns,” Inorganic Chemistry, vol. 41, no. 18, pp. 4732–4738, 2002. View at Publisher · View at Google Scholar · View at Scopus
  24. K. Riggle, T. Lynde-Kernell, and E. O. Schlemper, “Synthesis and X-ray structures of Ni(II) complexes of 1-(2-pyridinyl)ethanone oxime,” Journal of Coordination Chemistry Chemistry, vol. 25, pp. 117–125, 1992.
  25. R. Cibulka, I. Císařová, J. Ondráček, F. Liška, and J. Ludvík, “Electrochemical reductions of Ni2+, Cu2+ and Zn2+ complexes of azinyl methyl ketoximes on mercury,” Collection of Czechoslovak Chemical Communications, vol. 66, no. 1, pp. 170–184, 2001. View at Publisher · View at Google Scholar · View at Scopus
  26. R. A. Coxall, S. G. Harris, D. K. Henderson, S. Parsons, P. A. Tasker, and R. E. P. Winpenny, “Inter-ligand reactions: in situ formation of new polydentate ligands,” Journal of the Chemical Society, Dalton Transactions, no. 14, pp. 2349–2356, 2000. View at Publisher · View at Google Scholar
  27. C. Papatriantafyllopoulou, E. Manessi-Zoupa, A. Escuer, and S. P. Perlepes, “The sulfate ligand as a promising ‘player’ in 3d-metal cluster chemistry,” Inorganica Chimica Acta, vol. 362, no. 3, pp. 634–650, 2009. View at Publisher · View at Google Scholar
  28. S. Y. Nurova, E. P. Turevskaya, V. G. Kessler, and M. I. Yanovskaya, The Chemistry of Metal Alkoxides, Kluwer Academic Publishers, Dordrecht, The Netherlands, 2002.
  29. C. Papatriantafyllopoulou, A. Tasiopoulos, and S. P. Perlepes, unpublished results.
  30. C. Papatriantafyllopoulou, C. P. Raptopoulou, A. Terzis, J. F. Janssens, S. P. Perlepes, and E. Manessi-Zoupa, “Reactions of nickel(II) sulfate hexahydrate with methyl(2-pyridyl)ketone oxime: two mononuclear sulfato complexes containing the neutral ligand,” Zeitschrift für Naturforschung, vol. 62, no. 9, pp. 1123–1132, 2007. View at Scopus
  31. C. C. Stoumpos, T. C. Stamatatos, and T. C. Stamatatos, “Employment of methyl 2-pyridyl ketone oxime in manganese non-carboxylate chemistry: MnII2MnIV and MnII2MnIII6 complexes,” Dalton Transactions, no. 6, pp. 1004–1015, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  32. J. Zuo, J. Dou, D. Li, D. Wang, and Y. Sun, “Dichlorido[1-(2-pyrid-yl)ethanone oximato][1-(2-pyrid-yl)ethanone oxime]manganese(III),” Acta Crystallographica E, vol. 63, no. 12, pp. m3183–m3184, 2007. View at Publisher · View at Google Scholar · View at Scopus
  33. C. C. Stoumpos, T. C. Stamatatos, V. Psycharis, C. P. Raptopoulou, G. Christou, and S. P. Perlepes, “A new MnII4MnIII4 cluster from the use of methyl 2-pyridyl ketone oxime in manganese carboxylate chemistry: synthetic, structural and magnetic studies,” Polyhedron, vol. 27, no. 18, pp. 3703–3709, 2008. View at Publisher · View at Google Scholar · View at Scopus
  34. C. Papatriantafyllopoulou, G. Aromi, and G. Aromi, “Use of the sulfato ligand in 3d-metal cluster chemistry: a family of hexanuclear nickel(II) complexes with 2-pyridyl-substituted oxime ligands,” European Journal of Inorganic Chemistry, no. 18, pp. 2761–2774, 2007. View at Publisher · View at Google Scholar · View at Scopus
  35. P. Chaudhuri, M. Winter, U. Flörke, and H.-J. Haupt, “An effectively diamagnetic oximato-bridged asymmetric dinuclear copper(II) complex with a Cu(II)I bond,” Inorganica Chimica Acta, vol. 232, no. 1-2, pp. 125–130, 1995. View at Scopus
  36. A. B. P. Lever and E. Mantovani, “The far-infrared and electronic spectra of some bis-ethylenediamine and related complexes of copper(II) and the relevance of these data to tetragonal distortion and bond strengths,” Inorganic Chemistry, vol. 10, no. 4, pp. 817–826, 1971. View at Scopus
  37. K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds, Wiley, New York, NY, USA, 4th edition, 1986.
  38. C. Papatriantafyllopoulou, C. G. Efthymiou, and C. G. Efthymiou, “Initial use of the di-2-pyridyl ketone/sulfate ‘blend’ in 3d-metal cluster chemistry: preparation, X-ray structures and physical studies of zinc(II) and nickel(II) cubanes,” Journal of Molecular Structure, vol. 829, no. 1–3, pp. 176–188, 2007. View at Publisher · View at Google Scholar · View at Scopus
  39. C. Papatriantafyllopoulou, C. G. Efthymiou, C. P. Raptopoulou, A. Terzis, E. Manessi-Zoupa, and S. P. Perlepes, “Mononuclear versus dinuclear complex formation in nickel(II) sulfate/phenyl(2-pyridyl)ketone oxime chemistry depending on the ligand to metal reaction ratio: synthetic, spectral and structural studies,” Spectrochimica Acta A, vol. 70, no. 4, pp. 718–728, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  40. G. B. Deacon and R. J. Phillips, “Relationships between the carbon-oxygen stretching frequencies of carboxylato complexes and the type of carboxylate coordination,” Coordination Chemistry Reviews, vol. 33, pp. 227–250, 1980.