Heterobimetallic One-Dimensional Coordination Polymers MICuII (M = Li and K) Based on Ferromagnetically Coupled Di- and Tetracopper(II) Metallacyclophanes

The synthesis, crystal structure and magnetic properties of the coordination polymers of formula [EDAP{Li6(H2O)8[(Cu2(μ-mpba)2)2(H2O)2]}]n (1) and [(EDAP)2{K(H2O)4[Cu2(μ-mpba) 2(H2O)2]}Cl·2H2O]n (2), in which mpba = N,N′-1,3-phenylenebis(oxamate) and EDAP2+ = 1,1′-ethylenebis(4-aminopyridinium) are described. Both compounds have in common the presence of the [Cu2(mpba)2] tetraanionic unit which is a [3,3] metallacyclophane motif in which the copper(II) ions are five-coordinate in a distorted square pyramidal surrounding. The complex anion in 1 is dimerized through double out-of-plane copper to outer carboxylate-oxygen atoms resulting in the centrosymmetric tetracopper(II) fragment [Cu4(μ-mpba)4(H2O)2] which act as a ligand toward six hydrated lithium(I) cations leading to anionic ladder-like double chains whose charge is neutralized by the EDAP2+ cations. In the case of 2, each dicopper(II) entity acts as a ligand towards tetraquapotassium(I) units to afford anionic zig zag single chains of formula {K(H2O)4[Cu2(μ-mpba)2(H2O)2]}n plus EDAP2+ cations and non-coordinate chloride anions. Cryomagnetic measurements on polycrystalline samples 1 and 2 show the occurrence of ferromagnetic interactions between the copper(II) ions across the –Namidate–(C–C–C)phenyl–Namidate– exchange pathway [J = +10.6 (1) and +8.22 cm−1 (2)] and antiferromagnetic ones through the double out-of-plane carboxylate-oxygen atoms [j = −0.68 cm−1 (1), the spin Hamiltonian being defined as H = −J(SCu1·SCu2 + SCu2i ·SCu1i )− j(SCu2·SCu2i )].


Introduction
Nowadays molecular magnetism has become an interdisciplinary field in which scientists of different domains such as organic and inorganic chemistry, physical chemistry, condensed matter physics and biology have invested impressive research efforts.This diversity has led to a fast and significant progress of the different approaches of molecular magnetism, which depends on the nature of the spin carriers, these ones being organic radicals and/or paramagnetic metal ions [1,2].
More recently, oxamate-based compounds with higher nuclearity were prepared using two different strategies.One of them consists of the combination of the mpba ligand and first-or second-row transition metal ions described as "dimer of trimers" in which two Cu II −Pd II −Cu II trinuclear units are connected by two mpba ligands [25].The other one was the organic counterion modulated strategy in metathesis reactions with different (cat) 2 [Cu(opba)] [H 4 opba = N,N -1,2-phenylenediaminebis (oxamic acid)] building blocks resulting in dimers of Cu II arranged in supramolecular chains [26].Dealing with this last bis(oxamic) acid, some of its compounds have interesting catalytic properties and exhibit single-crystal-to single-crystal phase transitions [27][28][29][30].
Having in mind all those achievements with oxamate-based compounds, we decided to unite the possibility to play with supramolecular chemistry using the organic counterion EDAP 2+ [EDAP 2+ = 1,1 -ethylenebis(4-aminopyridinium)] featuring many sites of intermolecular interactions and the coordination versatility of the anionic [Cu 2 (µ-mpba) 2 ] 4− building block toward alkaline metal ions seeking out the synthesis of coordination polymers of varying dimensionalities and topologies (Scheme 1).In the following, we present the first results which concern the preparation, structural characterization and cryomagnetic investigation of the heterobimetallic compounds of formula

Starting Materials
The reagents and solvents were purchased from Sigma Aldrich and they were used as received.The diethyl ester form of the mpba ligand (Et2H2mpba proligand) and the (EDAP)Cl2•2H2O salt were synthesized by following previously reported methods [12,26].Elemental analyses (C, H and N) were performed with a Perkin-Elmer 2400 elemental analyzer.The lithium and copper contents were determined by atomic absorption spectrometry with a Hitachi Z-8200 Polarized Atomic Absorption Spectrophotometer.Infrared spectra were recorded on a Perkin Elmer 882 spectrophotometer in the range 4000 and 400 cm −1 using dry KBr pellets.Thermal analyses (TG curves) of 1 and 2 were carried in alumina crucibles sample holing on a Shimadzu TGA-60 using dynamic nitrogen atmosphere (see Supplementary Information, Figures S1 and S2).X-ray diffraction patterns for 1 and 2 were obtained by means of a Rigaku/eirgeflex diffractometer working at room temperature.Diffraction data were collected in the Bragg/Brentano mode (deg•s −1 ) using monochromatic Cu-Kα radiation (see Supplementary Information, Figures S3 and S4).

Starting Materials
The reagents and solvents were purchased from Sigma Aldrich and they were used as received.The diethyl ester form of the mpba ligand (Et 2 H 2 mpba proligand) and the (EDAP)Cl 2 •2H 2 O salt were synthesized by following previously reported methods [12,26].Elemental analyses (C, H and N) were performed with a Perkin-Elmer 2400 elemental analyzer.The lithium and copper contents were determined by atomic absorption spectrometry with a Hitachi Z-8200 Polarized Atomic Absorption Spectrophotometer.Infrared spectra were recorded on a Perkin Elmer 882 spectrophotometer in the range 4000 and 400 cm −1 using dry KBr pellets.Thermal analyses (TG curves) of 1 and 2 were carried in alumina crucibles sample holing on a Shimadzu TGA-60 using dynamic nitrogen atmosphere (see Supplementary Information, Figures S1 and S2).X-ray diffraction patterns for 1 and 2 were obtained by means of a Rigaku/eirgeflex diffractometer working at room temperature.Diffraction data were collected in the Bragg/Brentano mode (deg•s −1 ) using monochromatic Cu-Kα radiation (see Supplementary Information, Figures S3 and S4).

Synthesis of [EDAP{Li
Compound 1 was prepared by the one-step reaction of the Et 2 H 2 mpba proligand with copper(II) nitrate trihydrate and lithium(I) hydroxide (1:1:4.2molar ratio) in water plus a further addition of (EDAP)Cl 2 •2H 2 O.The detailed procedure is as follows: an aqueous solution (5 mL) of Cu(NO 3 ) 2 •3H 2 O (0.24 g, 1.0 mmol) was added dropwise to an aqueous solution (15 mL) of Et 2 H 2 mpba (0.308 g, 1.0 mmol) and LiOH•H 2 O (0.167 g, 4.2 mmol) with stirring at room temperature.The resulting deep-green solution was filtered to discard any solid particle.Then, an aqueous solution (5 mL) of (EDAP)Cl 2 •2H 2 O (0.323 g, 1.0 mmol) was added dropwise and the pale green solution was left to crystallize at room temperature.X-ray quality green needles of 1 were grown after 3 days.The crystals were filtered and dried on filter paper at room temperature.Yield: 0.227 g, 54%.Anal.
Compound 2 was prepared by the one-step reaction of the corresponding Et 2 H 2 mpba proligand with copper(II) nitrate and potassium hydroxide (1:1:4.2molar ratio) in water with further addition of (EDAP)Cl 2 •2H 2 O.The detailed procedure is as follows: an aqueous solution (5 mL) of Cu(NO 3 ) 2 •3H 2 O (0.24 g, 1.0 mmol) was added dropwise to an aqueous solution (15 mL) of Et 2 H 2 mpba (0.308 g, 1.0 mmol) and KOH (0.235 g, 4.2 mmol) with stirring at room temperature and the resulting deep-green solution was filtered to discard any solid particle.Then, an aqueous solution (5 mL) of (EDAP)Cl 2 2H 2 O (0.323 g, 1.0 mmol) was added dropwise.Green needles of 2 suitable for X-ray experiments separated from the resulting pale green solution on standing at room temperature after several days.

Crystallographic Data Collection and Refinement
Single crystal X-ray diffraction data were collected on an Oxford-Diffraction GEMINI-Ultra diffractometer (LabCri) at 150 K using Mo Kα radiation (λ = 0.71073 Å).The program CrysAlisPro [31] was used for data integration, scaling of the reflections and analytical absorption corrections.Final unit cell parameters were based on the fitting of all reflections positions.Non-merohedral twinning was observed for both compounds and the data were treated using also CrysAlisPro with two domains.The space group identification was done with XPREP [32] and the crystal structures were solved with direct methods with SIR-92 [33].The refinements were performed using SHELXL2018 [34] based on F 2 through full-matrix least-squares routine, using the WinGX [35] graphical user interface.All non-hydrogen atoms, except for the disordered ones, were refined anisotropically, and the hydrogen atoms were placed at calculated positions and refined isotropically with a riding model.Disordered atoms, except for those from crystallization water molecules in both structures, were split into two positions with occupancy refined independently for each disordered moiety.The crystallization water molecules were placed in electronic maxima not bonded to the rest of the structure with free refined occupancy.A summary of the crystal data, experimental details, and refinement results for 1 and 2 is given in Table 1 in which whereas selected bond lengths and angles are grouped in Table 2 (1) and Table 3 (2).Crystallographic data for the structures of 1 and 2 have been deposited at the Cambridge Crystallographic Data Centre with CCDC reference numbers 1846817 (1) and 1846818 (2).

Magnetic Measurements
The magnetic susceptibility measurements were carried out on crushed single crystals of 1 and 2 in the temperature range 2.0-300 K with a Quantum Design SQUID magnetometer and using applied magnetic fields of 0.5 T (T ≥ 100 K) and 1000 G (2.0 ≤ T < 100 K).Diamagnetic corrections of the constituent atoms were estimated from Pascal's constants [36] as −749 × 10 −6 (1) and −620 × 10 −6 cm 3 mol −1 (2) [per two copper(II) ions in both cases].Corrections for the temperature-independent paramagnetism [60 × 10 −6 cm 3 •mol −1 per copper(II) ion] and for the magnetization of the sample holder (a plastic bag) were also applied.

Description of the Crystal Structures of 1 and 2
Compound 1 crystallizes in the triclinic space group P1, with the asymmetric unit composed by a dicopper(II) [Cu 2 (µ-mpba) 2 ] 4− unit (Figure 1a), in which three lithium(I) cations are coordinated to it.In order to reach the charge balance, half of EDAP 2+ cation appears in this asymmetric unit together with coordinated water molecules to the lithium(I) cations.The two copper(II) ions of the dinuclear fragment (Cu1 and Cu2) are coordinated to two oxamate groups from two mpba 4− ligands in a bidentate form.Due to the geometrical constraints of this ligand, it cannot adopt the tetradentate coordination mode observed in its parent ligand in which the two oxamate substituents are in ortho position; however, a cis-CuN 2 O 2 coordination sphere occurs in relation to the bidentate oxamate groups.The resulting [3,3] The copper atoms are shifted from the mean basal plane by 0.261 (Cu1) and 0.135 Å (Cu2) towards the apical position.The values for the trigonality parameter (τ) are equal to 0.015 (Cu1) and 0.057 (Cu2) (τ = 0 and 1 for ideal square pyramidal and trigonal bipyramidal, respectively) [37].
This unusual coordination mode for meta-substituted bis-oxamate ligand in 1 is reported here for the first time, despite it has been already described for ortho [26, 38,39] and para [40] derivatives.It is important to point out that several counterions were used to obtain [Cu 2 (µ-mpba) 2 ] 4− complexes in the literature such as Na + [12], Li + [41,42], methylviologen (MV 2+ ) [43] 1-alkyl-3-methylimidazolium [C 4 MIm] + [44] and (S)-1-phenylethyl-trimethylammonium [(S)-(1-PhEt)Me 3 N] + [45] for instance, as described in the literature.In these cases, the resulting structures were composed by the [3,3] metallacyclophane-type motif of dicopper(II) ions in a dinuclear entity containing mpba as ligand.The EDAP 2+ dication combined with Li + ions in the presence of the metallacyclophane [Cu 2 (µ-mpba) 2 ] 2-moiety led to the tetranuclear copper(II)-oxamate unit, compound 1, which is the unique tetracopper(II) example reported in the literature so far.Besides that, it has already been shown that the EDAP 2+ cation as an additional templating counterion is justified by its ability to establish both hydrogen bonds and π−π interactions in the solid state due to the presence of the amino substituents at the pyridinium aromatic rings [26].
Six lithium(I) cations [Li1, Li2, Li3, Li1 i , Li2 ii , Li3 and Li3 i ; symmetry code: (ii) = x, 1 − y, z] are bound to each tetranuclear [{Cu 2 (µ-mpba) 2 } 2 ] 8− unit, four of them (Li1, Li2, Li1 i and Li2 ii ) being coordinated by two double carbonyl groups of two oxamate groups from two mpba ligands belonging to two tetranuclear units.These four alkaline cations exhibit a distorted square pyramidal surrounding, which is defined by one water molecule in the apical position and four oxamate-oxygens in the basal plane.The values of τ are equal to 0.06 (Li1 and Li1 i ) and 0.02 (Li2 and Li2 ii ) and they are shifted from the mean basal planes by 0.46 (Li1 and Li1 ii ) and 0.31 Å (Li2 and Li2 ii ) towards the apical site.The two remaining lithium atoms (Li3 and Li3 ii ) are also bonded to two tetracopper(II) units, but the coordination to the oxamate group in a monodentate form shares one oxygen atom of a carboxylate group with other lithium(I) ion.They are four-coordinate in a tetrahedral geometry with two water molecules completing the coordination sphere.Lithium(I) ions connect the tetranuclear units along the crystallographic b axis extending the motif to an 1D coordination polymer {Li 6 (H 2 O) 8 [Cu 4 (µ-mpba) 4 (H 2 O) 2 ]} 2− , in which the copper(II) ions separated along lithium bridges are distant from each other by 10.371(2) Å (Figure 2a).The resulting ladder-like double chain structure is interlinked through the EDAP 2+ cations, these counterions joining the ladders along the crystallographic c axis by means of hydrogen bonds involving their terminal NH 2 groups and the carboxylate oxygen atoms (Figure 2b).Since the EDAP 2+ cations in this compound show the anti conformation around their CH 2 -CH 2 centers, the pyridyl groups are not coplanar and occupy different layers, interconnecting ladders from different crystal packing layers and guaranteeing the 3D structure.2a).The resulting ladder-like double chain structure is interlinked through the EDAP 2+ cations, these counterions joining the ladders along the crystallographic c axis by means of hydrogen bonds involving their terminal NH2 groups and the carboxylate oxygen atoms (Figure 2b).Since the EDAP 2+ cations in this compound show the anti conformation around their CH2-CH2 centers, the pyridyl groups are not coplanar and occupy different layers, interconnecting ladders from different crystal packing layers and guaranteeing the 3D structure.Compound 2 is made up of [Cu2(μ-mpba)2(H2O)2] 4− dicopper(II) units which act as ligands towards tetraaquapotassium(I) entities, non-coordinated chloride anions and EDAP 2+ cations allowing the achievement of the electroneutrality (Figure 3a).Disordered crystallization water molecules are found filling the voids in the structure.Each crystallographically independent copper(II) ion in 2 (Cu1) is five-coordinate in a cis-CuN2O3 environment (Figure 3b), just as found for 1 and related compounds in the literature.The value of τ for this copper atom is equal to 0.01.Two oxamate groups from two mpba ligands occupy the basal plane and the apical site is filled by a water molecule.The copper(II) ion is slightly lifted from the mean basal plane, being 0.03 Å above it.The copper-copper separation within the [3,3] metallacyclophane-type unit in 2 is equal to 7.056(1) Å and the angle between the basal planes of each copper atom is 47.4(1)°.This smaller angle, compared to 1, is most likely caused by the potassium coordination to both carboxylate groups, forming double Cu-(μ-O)2-K bridges [Cu1-O1-K1 and Cu1-O4 i -K1; symmetry code (i) = 5/2 − x, y, 2 − z] which tide the carboxylate groups and force their approximation and thus a more distorted square base at the copper atom [the carboxylate oxygen atoms in 1 are 2.754(1) Å far from each other whereas they are 2.675(1) Å in 2].The distortions are also observed in the phenyl rings.Since the carboxylate groups are close, the phenyl rings are farther than in 1, with their geometric centers at 3.44 Å and their mean planes forming a dihedral angle of 9.15(1)°.
Each potassium cation in 2 is eight-coordinate with four carboxylate-oxygens and four water molecules building a distorted square antiprism geometry (Figure 3c).Like in 1, the alkaline cation extends the structure into 1D coordination polymers of formula {K(H2O)4[Cu2(μ-mpba)2(H2O)2]}n 3n− , differently from 1 in which the alkaline ion is coordinated by the carbonyl amide and the carboxylate Compound 2 is made up of [Cu 2 (µ-mpba) 2 (H 2 O) 2 ] 4− dicopper(II) units which act as ligands towards tetraaquapotassium(I) entities, non-coordinated chloride anions and EDAP 2+ cations allowing the achievement of the electroneutrality (Figure 3a).Disordered crystallization water molecules are found filling the voids in the structure.Each crystallographically independent copper(II) ion in 2 (Cu1) is five-coordinate in a cis-CuN 2 O 3 environment (Figure 3b), just as found for 1 and related compounds in the literature.The value of τ for this copper atom is equal to 0.01.Two oxamate groups from two mpba ligands occupy the basal plane and the apical site is filled by a water molecule.The copper(II) ion is slightly lifted from the mean basal plane, being 0.03 Å above it.The copper-copper separation within the [3,3]  Each potassium cation in 2 is eight-coordinate with four carboxylate-oxygens and four water molecules building a distorted square antiprism geometry (Figure 3c).Like in 1, the alkaline cation extends the structure into 1D coordination polymers of formula {K(H 2 O) 4 [Cu 2 (µ-mpba) 2 (H 2 O) 2 ]} n 3n− , differently from 1 in which the alkaline ion is coordinated by the carbonyl amide and the carboxylate groups.The single chains in 2 exhibit a zig zag conformation using the intrinsic bend of the 1,3-substituted ligand, as pictured in Figure 4a.This pattern raises along the crystallographic a axis and voids filled with the two disordered crystallization water molecules (the number of crystallization water molecules was determined by TG/DTA analysis) can be found along the crystallographic b axis.Finally, the 1D coordination polymers are packed in the crystallographic ac plane and they are intercalated with layers of EDAP 2+ cations (Figure 4b).
groups.The single chains in 2 exhibit a zig zag conformation using the intrinsic bend of the 1,3substituted ligand, as pictured in Figure 4a.This pattern raises along the crystallographic a axis and voids filled with the two disordered crystallization water molecules (the number of crystallization water molecules was determined by TG/DTA analysis) can be found along the crystallographic b axis.Finally, the 1D coordination polymers are packed in the crystallographic ac plane and they are intercalated with layers of EDAP 2+ cations (Figure 4b).The crystallization water molecules were omitted in both figures for the sake of clarity.

Magnetic Study
Magnetic properties of 1 in the form of the χMT versus T plot [χM is the magnetic susceptibility per four copper(II) ions] are shown in Figure 5. χMT at 300 K is equal 1.59 cm 3 mol −1 K, a value which is consistent with the presence of four magnetically isolated spin doublets (ca.1.58 cm 3 mol -1 K for SCu = ½ and gCu = 2.05).Upon cooling, a smooth increase of χMT occurs below 100 K to reach a maximum of 1.98 cm 3 mol -1 K at 9.0 K and exhibiting a further decrease to 1.77 cm 3 mol -1 K at 2.0 K.This plot is typical of an overall ferromagnetic behavior, the small decrease at very low temperatures being most likely due to very weak (intra/intermolecular) antiferromagnetic interactions and/or zerofield splitting effects.No maximum of χM is observed in the χMagainst T plot (see inset in Figure 5).
Having in mind the tetracopper(II) unit of 1 and aiming at evaluating the magnitude and nature of the magnetic interactions in this compound, its magnetic data were analyzed through the Hamiltonian of equation ( 1):

S S S S S S S S S S
(1) in which J and j are the magnetic coupling parameters between the copper(II) ions across the meta substituted phenyl ring of the mpba ligand and through the double out-of-plane carboxylate(oxamate)-oxygen exchange pathway, respectively.An average Landé factor (g = gCu1 = gCu2) was assumed for the two crystallographically independent copper(II) in order to avoid any overparametrization.The deduced analytical expression is given by equation (2) [46]: A    j J

Magnetic Study
Magnetic properties of 1 in the form of the χ M T versus T plot [χ M is the magnetic susceptibility per four copper(II) ions] are shown in Figure 5. χ M T at 300 K is equal 1.59 cm 3 mol −1 K, a value which is consistent with the presence of four magnetically isolated spin doublets (ca.1.58 cm 3 mol −1 K for S Cu = 1 /2 and g Cu = 2.05).Upon cooling, a smooth increase of χ M T occurs below 100 K to reach a maximum of 1.98 cm 3 mol −1 K at 9.0 K and exhibiting a further decrease to 1.77 cm 3 mol −1 K at 2.0 K.This plot is typical of an overall ferromagnetic behavior, the small decrease at very low temperatures being most likely due to very weak (intra/intermolecular) antiferromagnetic interactions and/or zero-field splitting effects.No maximum of χ M is observed in the χ M against T plot (see inset in Figure 5).
Having in mind the tetracopper(II) unit of 1 and aiming at evaluating the magnitude and nature of the magnetic interactions in this compound, its magnetic data were analyzed through the Hamiltonian of equation ( 1): in which J and j are the magnetic coupling parameters between the copper(II) ions across the meta substituted phenyl ring of the mpba ligand and through the double out-of-plane carboxylate(oxamate)-oxygen exchange pathway, respectively.An average Landé factor (g = g Cu1 = g Cu2 ) was assumed for the two crystallographically independent copper(II) in order to avoid any overparametrization.The deduced analytical expression is given by equation (2) [46]: in which N, β and k have their usual meanings.The best-fit parameters are: ).The calculated curve (solid line in Figure 5) reproduces well the magnetic data in the whole temperature range explored.The ferromagnetic interaction in 1 (J = +10.63cm −1 ) is unambiguously mediated by the double Cu1-N amidate -(C-C-C) phenyl -N amidate -Cu2 exchange pathway, being once more a nice example of the efficiency of the spin polarization mechanism to transmit ferromagnetic interactions between copper(II) ions separated by ca.7 Å in this type of meta-substituted bis-oxamate ligands [12,[47][48][49].The ferromagnetic coupling in this compound is explained by the spin polarization mechanism operating in the Cu-N amidate -C ring -C ring -C ring -N amide -Cu fragment.The alternating sign of the spin density in this pathway leads to the same sign on the two copper(II) ions.In comparison with the first dicopper(II) compound containing mpba ligands reported in literature Na J value for 1 is smaller than the one observed (see Table 4).This may be understood by comparing the values of the torsion angle (φ) involving the Cu-N amidate bonds and the aromatic spacers.The closer this angle is to 90 • and the greater the planarity of the aromatic spacer, the stronger is the ferromagnetic coupling through this pathway.This angle in 1 vary from 71.5(3) to 85.9(9) • , a value which is smaller than those occurring in the related compound Na Concerning the value of j (−0.68 cm −1 ), it unambiguously corresponds to the interaction between Cu1 and Cu1 i atoms through the double out-of-plane carboxylate(oxamate)-oxygen pathway.For such a situation, weak ferro-and antiferromagnetic couplings were reported in the literature, its sign and magnitude being dependent on subtle structural factors such as the value of the angle at the bridgehead oxygen and the apical copper-to oxygen bond length (see Table 4).Simple orbital symmetry considerations allow to understand this situation.For a copper(II) ion in a square pyramidal surrounding like Cu2 (and the symmetry related Cu2 i ), the unpaired electron is mainly defined by a d x 2 −y 2 magnetic orbital which spreads its density only over the basal plane, a poor spin density being expected on the apical site.Then, the overlap between the parallel magnetic orbitals of Cu2 and Cu2 i is predicted to be very weak leading to a very weak antiferromagnetic interaction.Depending on the value of the angle at the bridgehead oxygen, accidental orthogonality of the magnetic orbitals may result and the interaction would become weakly ferromagnetic.The j value found in 1 is in the range of those reported in the literature for the double out-of-plane copper(II)-carboxylate-oxygen bridged compounds, as shown in Table 4.The magnetic properties of 2 in the form of χMT against T plot [χMT is the magnetic susceptibility per two copper(II) ions] are shown in Figure 6.At room temperature, χMT is equal to 0.81 cm 3 mol -1 K, a value which is as expected for two magnetically non-interacting spin doublets.Upon cooling, this value remains practically constant until 150 K and it further increases continuously to reach 1.24 cm 3 mol -1 K at 2.0 K.This plot is typical of an overall ferromagnetic behavior.The magnetic properties of 2 in the form of χ M T against T plot [χ M T is the magnetic susceptibility per two copper(II) ions] are shown in Figure 6.At room temperature, χ M T is equal to 0.81 cm 3 mol −1 K, a value which is as expected for two magnetically non-interacting spin doublets.Upon cooling, this value remains practically constant until 150 K and it further increases continuously to reach 1.24 cm 3 mol −1 K at 2.0 K.This plot is typical of an overall ferromagnetic behavior.The magnetic properties of 2 in the form of χMT against T plot [χMT is the magnetic susceptibility per two copper(II) ions] are shown in Figure 6.At room temperature, χMT is equal to 0.81 cm 3 mol -1 K, a value which is as expected for two magnetically non-interacting spin doublets.Upon cooling, this value remains practically constant until 150 K and it further increases continuously to reach 1.24 cm 3 mol -1 K at 2.0 K.This plot is typical of an overall ferromagnetic behavior.The magnetic data of 2 were analyzed through the spin Hamiltonian for an isolated pair of isotropic metal ions [Equation ( 3)] in which J is the magnetic coupling parameter, S 1 = S 2 = 1 /2 and g is the isotropic Landé factor of the copper(II) ions.In this case, the equation derived from the Hamiltonian is the Bleaney-Bowers expression (equation ( 4)) [63]: A Curie-Weiss term (θ) was introduced in Equation ( 4) to take into account the possible intermolecular interactions.Best-fit parameters are: J = +8.22cm −1 , g = 2.07 and θ = +0.27K with R = 2.15 × 10 −4 .The magnetic coupling within the dicopper(II) [3,3] metallacyclophane fragment in 2 (J = +8.22cm −1 ) is of identical nature with that in 1 (J = +7.14cm −1 ), although it is somewhat smaller.The same spin polarization mechanism involved in 1 occurs in 2, but the different values of J found for them can be understood by a comparison of some structural parameters within their dicopper(II) fragments.The dihedral angle between the Cu-N amidate bond and the aromatic spacer in 2 [47.4(1) • ] is smaller than the corresponding one in 1 [59.2(2)• ], indicating that the spin polarization mechanism to mediate ferromagnetic interactions between copper(II) ions through this pathway would be more efficient in 1.This subtle structural difference accounts for the somewhat weakening of the ferromagnetic coupling when going from 1 to 2 [12,48].

Conclusions
This work shows that the use of templating organic counterions such as EDAP 2+ and coordinated alkaline cations may play a relevant structural role in the assembling of 1D coordination polymers with ladder-like double chain or zig zag chain structures depending on the nature of the univalent alkaline cation.Remarkably, the use of the lithium(I) leads to the tetranuclear copper(II)-oxamate unit in compound 1, in which two dicopper(II) [3,3] metallacyclophane-type entities are assembled throughout double out-of-plane interactions.As far as we know, it is the first time that such a tetracopper(II) unit with the mpba ligand is described.Although compound 1 presents a satisfactory R int indicator, due to intrinsic crystals quality and twinning, the refinement indicators are out of routine of the X-ray crystallography for small molecules, but its crystal structure is corroborated by chemical analysis and it matches the theoretical models based on it which were proposed to treat the magnetic properties.Compound 2 is obtained when the lithium(I) cations are replaced by the potassium(I) ones where this assembling does not occur and the dicopper(II) [3,3] metallacyclophane units are interconnected through the alkaline cations.Moderate ferromagnetic couplings between the copper(II) ions separated by more than ca.7.0 Å in the metallamacrocycles of the [3,3] metallacyclophane-type of 1 and 2 are observed, the spin polarization mechanism being responsible for them.Author Contributions: T.T.d.C. performed the synthesis of compounds and also the IR, elemental analyses and atomic absorption measurements.W.X.C.O.carried out X-ray diffraction measurements.E.F.P. took the magnetic measurements and calculated the best-fit curves.M.J. and F.L. interpreted all results and contributed to the revision of this manuscript.C.L.M.P. designed the synthesis, supervised all the experiments, interpreted all results and was the responsible scientist for Funding Acquisition.All authors contributed to the writing of the manuscript.
metallacyclophane-type motif of this dicopper(II) entity is also somewhat driven by π-stacking between the phenyl groups of the two mpba ligands which are placed very close (h = 3.38 Å between the geometric centers) and almost parallel [θ = 10.7(1)• from mean planes] to each other.The value of the dihedral angle between the basal planes of the copper atoms (Φ) is 59.2(2) • and the intermetallic distance (r) is equal to 7.030(1) Å.All these values are slightly different from those in the compound Na 4 [Cu 2 (µ-mpba) 2 ]•10H 2 O [12] (h = 3.36 Å, θ = 7.5 • , Φ= 58 • and r = 6.822Å, respectively).Cu1 and Cu2 are five-coordinate in somewhat distorted square pyramidal surroundings.Their basal planes are defined by the O1N1N2O4 (Cu1) and O7N3N4O10 (Cu2) sets of atoms whereas the apical sites are filled by a water molecule (O13 at Cu1) and a carboxylate-oxygen from an oxamate group of an adjacent [Cu 2 (µ-mpba) 2 ] 4− unit [O10 i at Cu2; symmetry code:
metallacyclophane-type unit in 2 is equal to 7.056(1) Å and the angle between the basal planes of each copper atom is 47.4(1) • .This smaller angle, compared to 1, is most likely caused by the potassium coordination to both carboxylate groups, forming double Cu-(µ-O) 2 -K bridges [Cu1-O1-K1 and Cu1-O4 i -K1; symmetry code (i) = 5/2 − x, y, 2 − z] which tide the carboxylate groups and force their approximation and thus a more distorted square base at the copper atom [the carboxylate oxygen atoms in 1 are 2.754(1) Å far from each other whereas they are 2.675(1) Å in 2].The distortions are also observed in the phenyl rings.Since the carboxylate groups are close, the phenyl rings are farther than in 1, with their geometric centers at 3.44 Å and their mean planes forming a dihedral angle of 9.15(1) • .

Figure 4 .
Figure 4. (a) View of the packing of two adjacent heterobimetallic chains along the crystallographic a axis in 2. EDAP 2+ cations are omitted for clarity.(b) Intercalated layers of EDAP 2+ cations separating the layers of {K(H2O)4[Cu2(μ-mpba)2(H2O)2]}n 3n− polymers packed along the crystallographic ab plane.The crystallization water molecules were omitted in both figures for the sake of clarity.

Figure 4 .
Figure 4. (a) View of the packing of two adjacent heterobimetallic chains along the crystallographic a axis in 2. EDAP 2+ cations are omitted for clarity.(b) Intercalated layers of EDAP 2+ cations separating the layers of {K(H 2 O) 4 [Cu 2 (µ-mpba) 2 (H 2 O) 2 ]} n 3n− polymers packed along the crystallographic ab plane.The crystallization water molecules were omitted in both figures for the sake of clarity.

Table 1 .
Summary of Crystallographic Data for 1 and 2.