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Article

Modification of Structure and Magnetic Properties in Coordination Assemblies Based on [Cu(cyclam)]2+ and [W(CN)8]3−

by
Aleksandra Pacanowska
,
Mateusz Reczyński
and
Beata Nowicka
*
Jagiellonian University in Krakow, Faculty of Chemistry, Gronostajowa 2, 30-387 Kraków, Poland
*
Author to whom correspondence should be addressed.
Crystals 2019, 9(1), 45; https://doi.org/10.3390/cryst9010045
Submission received: 14 December 2018 / Revised: 6 January 2019 / Accepted: 10 January 2019 / Published: 16 January 2019
(This article belongs to the Special Issue Molecular Magnets)
Browse Figures
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Abstract

:
The 1D {[CuII(cyclam)]3[WV(CN)8]2.5H2O}n (1·5H2O) (cyclam = 1,4,8,11-tetraazacyclotetradecane) coordination polymer of ladder topology can be obtained in water-alcohol solution from [Cu(cyclam)]2+ and [W(CN)8]3− building blocks. Upon dehydration, 1·5H2O undergoes a single-crystal-to-single-crystal structural transformation to the anhydrous {[CuII(cyclam)]3[WV(CN)8]2}n (1) form, which retains the same topology, but is characterized by shorter Cu-W distances and significantly more bent CN-bridges. The deformation of the coordination skeleton is reflected in magnetic properties: the predominant intra-chain interactions change from ferromagnetic in 1·5H2O to antiferromagnetic in 1. The reaction between the same building blocks in water solution under slow diffusion conditions leads to the formation of a 0D {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O pentanuclear assembly (2·3H2O).

Graphical Abstract

1. Introduction

One of the interesting features that can be achieved in molecular magnetics is the possibility to modify magnetic properties by sorption of small guest molecules. At the turn of the century magnetic sponges was defined as compounds that change structure and magnetic properties upon reversible removal of coordinated or non-coordinated water molecules [1,2,3]. Later, the term solvatomagnetism was introduced to describe changes in magnetic behavior upon sorption or desorption of different guest molecules.
We have previously shown that the solvatomagnetic effect can be repeatedly observed in CN-bridged networks containing the [Ni(cyclam)]2+/3+ cationic building block. By combining it with different polycyanometallates, we obtained two main families of coordination polymers of 1D and 2D connectivity. The 2D {[NiII(cyclam)]3[M(CN)n]2}∞ (M = CrIII, FeIII, n = 6; M = WV, n = 8) networks [4,5,6,7] show honeycomb-like topology with microporous channels running across the coordination layers. For these networks, we observed formation of different hydrates as well as the possibility to introduce small organic molecules. For each of the three compounds, four pseudopolymorphic forms differing in structure and magnetic properties have been characterized. The second family of solvatomagnetic polymers are non-porous 1D bimetallic alternating chains. The {[NiIII(cyclam)][MIII(CN)6]2∙6H2O}∞ (MIII = Cr, Fe) [8] chains can be reversibly dehydrated, which affects their magnetic properties. The {(H3O)[NiIII(cyclam)][MII(CN)6]2∙5H2O}∞ (MII = Fe, [9] Ru, Os [10]) chains, where the charge of the coordination skeleton is compensated by the presence of the H3O+ ions, are rare examples of sorption-driven charge-transfer. The removal of water causes partial electron transfer from MII centers to NiIII ions. The process is reversible for FeII and irreversible for RuII and OsII—based compounds.
Cyclam complexes with different metal centers, including NiII [11,12], CuII [13,14,15,16,17] and MnIII [18,19,20], were often used to build CN-bridged coordination polymers. However, apart from our studies, there are no reports on the desolvation effects in this group of compounds. Thus, we decided to examine the potential of cyclam complexes with other metal ions for the construction of solvatomagnetic materials. The manganese(III)-based alternating bimetallic chains {[NiIII(cyclam)][MIII(CN)6]2∙6H2O}∞ (MIII = Cr, Fe) exhibit loss of crystallization water accompanied by structural and magnetic changes [21]; however, in contrast to their NiIII-based congeners [8], the dehydration process was irreversible. The CuII cationic building blocks often differ from those of other 3d metals, due to the strong Jahn-Teller effect. The {[CuII(cyclam)]3[WV(CN)8]2∙5H2O}n compound [22] shows 1D ladder-like topology, unlike the series of NiII-based 2D honeycomb-like networks of the same stoichiometry described above. It was characterized in terms of structure and magnetic properties, but dehydration effect was not mentioned in the report [22]. Here, we present the post-synthetic modification of structure and magnetic properties of this ladder chain network and the synthesis of a new 0D assembly based on the same building blocks.

2. Materials and Methods

The Na3[W(CN)8]·4H2O precursor complex was prepared according to the published procedure [23]. Other reagents and solvents were commercially available and used as supplied. Measurements of powder X-ray diffraction were carried out on a PANanalitical X’Pert Pro powder diffractometer with the Cu Kα radiation source. Elemental analysis for carbon, nitrogen and hydrogen were carried out on a Vario Micro Cube elemental analyser. IR spectra of single crystals were recorded using a Nicolet iN10 MX FTIR microscope operating in the transmission mode. The dehydration process was characterized by a dynamic vapor sorption method using an SMS DVS Resolution apparatus in the 40–0% RH range at 298 K. Magnetic measurements were performed on a Quantum Design MPMS3 magnetometer. Variable-temperature magnetic susceptibility was measured at an applied field of 1000 Oe in the temperature range of 300 K to 1.8 K and magnetization at 1.8 K up to 70 kOe. The samples were sealed in polyethylene bags to avoid dehydration at low pressure.

2.1. Synthesis of the [Cu(cyclam)](NO3)2·6H2O Precursor Complex

The compound was prepared according to the modified published procedure [24]. Cu(NO3)2·3H2O (1 mmol, 245.4 mg) was dissolved in 4 ml of absolute ethanol at 60 °C. To the above solution, solid cyclam (1 mmol, 200.0 mg) was added and immediate precipitation of violet product was observed. The suspension was left in the freezer for 1h and then filtered. Yield: 396.0 mg (79%).

2.2. Synthesis of {[Cu(cyclam)]3[W(CN)8]2·5H2O}n (1·5H2O)

The compound was prepared according to the modified published procedure [22]. A solution of [Cu(cyclam)](NO3)2·6H2O (0.13 mmol, 66.4 mg) in a water-ethanol mixture (1:2, 20 mL) was layered over a solution of Na3[W(CN)8]·4H2O (0.07 mmol, 35.6 mg) in a water-ethanol mixture (2:1, 20 mL) in test tubes. Brownish-red needle-shaped crystals were formed after three days. (Found: C, 33.53; H, 4.976; N, 23.44; calc. C46H82Cu3N28O5W2: C, 33.17; H, 4.96; N, 23.55) IR νCN: 2167 cm−1, 2151 cm−1, 2145 cm−1, 2139 cm−1.

2.3. Synthesis of {[Cu(cyclam)]3[W(CN)8]2}n (1)

The anhydrous compound was obtained by drying 1·5H2O at 50 °C for 1 h. IR νCN: 2166 cm−1, 2161 cm−1, 2151 cm−1, 2144 cm−1, 2139 cm−1, 2134 cm−1

2.4. Synthesis of {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O (2·3H2O)

The solutions of [Cu(cyclam)](NO3)2·6H2O (0.05 mmol, 26.8 mg in 8 mL of H2O) and Na3[W(CN)8]·4H2O (0.03 mmol, 14.5 mg in 8 mL of H2O) were placed in separate sections of an H-tube and water was added to fill the horizontal connecting tube. Brownish-red plate-shaped crystals were formed after 2–3 weeks. (Found: C, 33.42; H, 4.76; N, 23.53; cal. C46H82Cu3N28O5W2: C, 33.17; H, 4.96; N, 23.55). IR νCN: 2166 cm−1, 2151 cm−1, 2144 cm−1, 2139 cm−1.

2.5. Structure Determination

Single crystal X-ray diffraction measurements for 1 and 2·3H2O were performed on a Bruker D8 QUEST diffractometer. The structures were solved by direct methods using SHELXT [25]. Refinement and further calculations were carried out using SHELXL [25]. The non-H atoms were refined anisotropically, apart from some O atoms of disordered crystallization water, which were refined isotropically. H—atoms were placed in idealized positions and refined using riding model. H—atoms were not considered for disordered water molecules in 2·3H2O; however, they were included in the calculation of the molecular weight. The unit cell of 1 was transformed in order to allow direct comparison to the structure of 1·5H2O, therefore it does not conform to the requirements of a reduced cell. Due to high absorption and relatively poor quality of the crystals of 1 after solid state transformation, some residual electron density peaks appear around W. The crystallographic data for 1 and 2·3H2O are presented in Table 1, with structure parameters for 1·5H2O [22] added for comparison. Graphics were created with Mercury 3.9.10. The analysis of coordination polyhedra was performed using SHAPE 2.1 [26]. CCDC 1885028 and 1885029 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html

3. Results and Discussion

3.1. Synthesis and Post-Synthetic Modification

The reaction between [Cu(cyclam)]2+ and [W(CN)8]3- building blocks in water-alcohol solution leads to the formation of {[CuII(cyclam)]3[WV(CN)8]2.5H2O}n (1·5H2O) of the ladder-chain structure reported earlier [22]. The crystals of 1·5H2O are stable under ambient conditions, but at slightly elevated temperatures (30–50 °C), they lose crystallization water to result in an anhydrous {[CuII(cyclam)]3[WV(CN)8]2}n (1) form. The process occurs with retention of crystallinity and thus the structure of 1 could be established from a single crystal XRD measurement. The single-crystal-to-single-crystal structural transformations upon desolvation are relatively rare [5,27,28]. In the family of the coordination polymers based on [Ni(cyclam)]2+/3+ ions and polycyanometallates, we observed this phenomenon only for the 2D {[NiII(cyclam)]3[WV(CN)8]2}∞ network [5]. The crystals of 1 exposed at 25 °C to humid air (40–60% RH) regain their original composition. However, upon rehydration, the crystals collapse and the PXRD results (Figure S1) show that the rehydration process leads to a mixture of phases, one of which is the original 1·5H2O form. We followed the dehydration process using the gravimetric dynamic vapor sorption method. The sample was subjected to decreasing relative humidity from 40% to 0% at a constant temperature of 298K. The sharp decrease in mass starts at about 15% RH (Figure S2), and takes place in two unresolved steps, which correspond to the subsequent loss of 3 and 2 water molecules.
When the reaction between the same building blocks is carried out in a water solution under slow diffusion conditions, a 0D pentanuclear assembly of the formula {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2.3H2O} (2·3H2O) is obtained. Interestingly, quick precipitation from the water solution does not lead to the same result. The analysis of the PXRD patterns (Figure S3) suggests that 1·5H2O is formed instead. Similar disparity between the course of slow diffusion and quick precipitation reactions was observed for the 3D {[NiII(cyclam)]2[WIV(CN)8]}∞ network [29]. Due to a very low yield and long time taken to grow crystals, the dehydration of 2·3H2O was not studied, but it seems likely that both lattice and coordinated water could be removed, possibly with the formation of additional CN-bridges between neighboring molecules.

3.2. Description of Structures

Upon dehydration of 1·5H2O, the triclinic system and space group P-1 are retained, but cell parameters change significantly (Table 1). In particular, period c shortens by 1.7 Å (8.7%) and the γ angle decreases by 9.38° (13.5%). The cell volume decreases by 155 Å3 (9.6%) per formula unit, which corresponds quite well to the volume expected for five H-bound water molecules. The connectivity of the coordination network is retained, with Cu and W CN-bridged centers forming a 1D ladder-like chain. Apart from the removed water molecules, the asymmetric unit of 1 (Figure 1) contains the same set of atoms as 1·5H2O, including Cu1 and W1 ions located in general positions and Cu2 ions in the inversion center. Each tungsten center (W1) is coordinated by eight cyanide ligands, three of which form bridges to copper centers (two Cu1 and one Cu2). The copper ions are connected with two tungsten centers through cyanide bridges coordinated in axial positions, with equatorial positions blocked by the cyclam ligand. The dehydration process strongly affects the geometry of CN-bridges and coordination polyhedra. The Continuous Shape Measure analysis [26] shows that the geometry of the [W(CN)8]3− ion in the hydrated form 1·5H2O is close to square antiprism, while for the anhydrous form (1), it changes to a triangular dodecahedron (Table S1). Both Cu ions in 1·5H2O show a highly distorted octahedral geometry (Table S2), due to the significant Jahn-Teller effect causing elongation of the axial bonds. The non-centrosymmetric Cu1 center is more distorted, due to the asymmetry of the axial bonds, one of which (Cu1-N1 of 2.698 Å) can be classified as a semi-coordination bond. Upon dehydration, the Cu2-N5 distances shorten by 0.053 Å, while the Cu2-N distances become more symmetrical (Table 2). As an effect, the octahedral geometry of both copper centers in the anhydrous form 1 is less distorted (Table S2). The angles of cyanide bridges (Cu1-N1-C1, Cu1-N4-C4, Cu2-N5-C5) decrease by 13.74–24.78° (Table 2). Therefore, dehydration leads to significant shortening of the distances between the CN-linked metal centers by 0.219–0.392 Å.
Projections of structure along the crystallographic axes for 1·5H2O and 1 (Figure 2) show the ladder-like topology retained upon dehydration. In both structures, the ladders lie in the (11–1) plane and run along the [1,2,3,4,5,6,7,8,9,10] direction. However, the changes in the coordination geometry of the [W(CN)8]3− ion and different alignment of the cyclam ligand in both forms are noticeable. Likewise, the bending of the CN-bridges can be seen, particularly in the view along the a period. Upon dehydration, the distance between the neighboring chains in the [001] direction shortens, which is visible in the projections along the b and c axes. The distance between the Cu1 and W1 centers from the neighboring chains shortens by 0.725 Å. In the hydrated form 1·5H2O, the coordination ladders are bound into a 3D supramolecular network by H-bonds between cyanide ligands, NH groups of the cyclam molecules, and crystallization water [22]. Upon loss of crystallization water, the hydrogen bonds are rearranged (Figure S4). The ladders are bound into stacks along the [110] direction, resulting in the 2D supramolecular network. Conversely, there is no connection in the [001] direction, despite shorter distance between the ladders. Moreover, due to the bending of CN-bridges, intramolecular H-bonds appear. They link the terminal CN ligands with the NH groups of cyclam from the W1 and Cu1 centers, and thus stabilize strong bending of the Cu1-N1-C1 bridge (Table 2). This may be the reason why the rehydration process leads to the collapse of crystals and is not fully reversible.
The 0D {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O assembly (2·3H2O) is obtained from the same building blocks as the 1·5H2O ladder chain, but under different synthetic conditions. The compound crystallizes in a monoclinic system, space group P 21/n (Table 1). Its structure is composed of Z-shaped pentanuclear molecules containing two W and three Cu centers connected by CN-bridges with water molecules coordinated to the terminal Cu ions (Figure 3). There are two symmetrically independent molecules. Each of them is centrosymmetric with the central Cu ions located at the inversion centers. Therefore, the asymmetric unit consist of two tungsten and two copper centers (W1, W2, Cu1, Cu3) in general positions and two copper centers (Cu2 and Cu4) in special positions. Each W atom is coordinated by eight cyanide ligands, two of which form bridges to two Cu centers (W1 with Cu1 and Cu2; W2 with Cu3 and Cu4). The coordination geometry of both W centers is close to ideal square antiprism (Table S1). All Cu ions have cyclam ligand coordinated in equatorial positions. The centrosymmetric Cu2 and Cu4 atoms are linked by two cyanide bridges, whereas the Cu1 and Cu3 centers located at the ends of the Z-shaped molecule are coordinated by one cyanide bridge and one water molecule in axial positions. The octahedral coordination geometry is distorted due to the Jahn-Teller effect (Table S2). There is a large disproportion of the extent of this distortion between the centrosymmetric Cu centers: Cu2 with the very long and bent NC-bridges (Table 3) shows very large distortion, while Cu4 shows the lowest distortion among the Cu centers in 1 and 2.
The average length of the Cu-N bond in the CN-bridge is 2.543 Å, which is shorter than for 1·5H2O (2.588 Å) or 1 (2.565 Å). The average value of the Cu-N-C angles of the CN-bridges (147.87°) is closer to those observed in 1·5H2O (153.58°) than those in the anhydrous form 1 (132.31°). The distances between the CN-bridged metal centers are shorter for the central Cu (W1-Cu2, W2-Cu4) than for the terminal ones (W1-C1, W2-Cu3) by about 0.25 Å, due to the stronger bending of the central CN bridges.
Projection along the a and b crystallographic directions (Figure 4) shows that the symmetrically independent molecules (marked red and blue) are arranged in independent layers in the (10–1) and (20–2) planes. They are bound into a 3D supramolecular network by the net of hydrogen bonds between cyanide ligands, NH groups of cyclam, aqua ligands, and crystallization water (Figure S5). The molecules of the same symmetry are bound within the layers by H-bonds formed by coordinated water, which donates two protons to two CN ligands of two neighboring molecules. The layers are linked by direct bonds between CN ligands and NH groups, as well as by H-bonds between CN-ligands mediated by crystallization water.

3.3. Magnetic Properties

All compounds were characterized by DC susceptibility measurements at the applied field of 1000 Oe in the temperature range 1.8–300 K (Figure 5) and magnetization at 1.8K in the field up to 70 kOe (Figure 6). At the high temperature limit, the value of χT for all compounds is close to the Curie constant of 1.88 cm3K/mol, expected for three CuII and two WV ions with s = 1/2 and g = 2, and it remains constant down to about 60 K. Below that temperature, differences in magnetic behavior between the compounds become apparent. For 1·5H2O, where intra-chain interactions are predominantly ferromagnetic [22], the χT curve rises slightly to reach the maximum of 2.03 cm3K/mol at 7.5 K. For the dehydrated sample 1, the χT value decreases below 60 K down to 0.87 cm3K/mol at 1.8 K, indicating predominantly antiferromagnetic interaction within the chains. This change in magnetic behavior can be attributed to the bending of the CN-bridges. As was shown before [30,31,32] for d9 configuration, the bridge geometry strongly affects the character and strength of magnetic superexchange through the π* orbitals of CN– ions, which changes from ferromagnetic for a linear bridge to antiferromagnetic for strongly bent bridges. The antiferromagnetic character of intra-chain interactions in 1 is also visible in the magnetization at 1.8 K. The increase of the magnetic moment in an increasing field is much slower for the dehydrated sample 1 than for 1·5H2O and it reaches only 2.98 Nβ at 70 kOe, which is far from the expected saturation value of 5 Nβ. The magnetic characteristic that we obtained for 1·5H2O is very similar, but not identical with the published data [22]. Slightly lower values of magnetization and high-temperature susceptibility are most probably caused by the relatively low accuracy of small sample weight assessment. The difference in the χT course in the low temperature range, where we observed a lower maximum at a slightly higher temperature, may be due to partial loss of water and onset of the structural transformation in one of the samples.
The magnetic behavior of 2·3H2O is similar to that of 1·5H2O. In the χT dependence on T (Figure 5), a slight increase below 60 K is observed with a broad maximum of 2.01 cm3K/mol at about 14 K and an abrupt drop below 7 K. The magnetization curve lies slightly below the one of 1·5H2O and at 70 kOe reaches 4.37 Nβ (Figure 6). These results suggest the presence of weak intramolecular ferromagnetic interactions. This is consistent with the observed geometry of CN-bridges, which in 2·3H2O is similar to that in 1·5H2O.

4. Conclusions

We have shown that similarly to [Ni(cyclam)]2+/3+ complexes, the [Cu(cyclam)]2+ ion can be used as a cationic building block in combination with polycyanometallates to construct solvatomagnetic coordination networks. The 1D {[CuII(cyclam)]3[WV(CN)8]2.5H2O}n (1·5H2O) polymer exhibits a rare single-crystal-to-single-crystal structural transformation to the anhydrous {[CuII(cyclam)]3[WV(CN)8]2}n (1) form. Although the topology of the compound is retained, the modification of bonds geometry and intermolecular interactions results in a noticeable change of magnetic properties, switching the predominant intra-chain interactions from ferromagnetic in 1·5H2O to antiferromagnetic in 1. The dehydration process is not fully reversible, probably due to the formation of intra-chain H-bonds, which stabilize strong bending of the CN-bridges. The rehydration causes collapse of the crystals and partial degradation of the sample. Apart from the post-synthetic modification of 1·5H2O, we have also shown that the same building block can be arranged in a different structure by slight modification of synthetic conditions. The {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O pentanuclear Z-shaped molecule (2·3H2O), obtained from water under slow diffusion conditions, exhibits weak ferromagnetic interactions through CN-bridges.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4352/9/1/45/s1, Figure S1: PXRD pattern for the rehydrated sample of 1 in comparison to 1∙5H2O and 1; Figure S2: Mass loss upon dehydration of 1∙5H2O monitored by dynamic vapor sorption method; Figure S3: PXRD pattern for sample obtained from [Cu(cyclam)](NO3)2 and Na3[W(CN)8] by quick precipitation from water solution in comparison to 1∙5H2O and 2∙3H2O; Table S1: Continuous shape measure parameters for octa-coordinated W centers in the structures of 1∙5H2O, 1 and 2∙3H2O; Table S2: Continuous shape measure parameters for hexa-coordinated Cu centers of 1∙5H2O, 1 and 2∙3H2O; Figure S4: Inter- and intra-chain H-bonds in 1; Figure S5: Inter- and intra-molecular H-bonds in 2·3H2O.

Author Contributions

Syntheses, original draft preparation: A.P.; crystal structures: A.P. and B.N.; magnetic characterization: M.R.; conceptualization, supervision, funding acquisition and project administration, manuscript review and editing: B.N.

Funding

This research was funded by Polish National Science Centre, grant number 2015/19/B/ST5/00922.

Conflicts of Interest

The authors declare no conflict of interest.

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Crystals 09 00045 g001 550
Figure 1. The asymmetric unit of 1 with atom numbering; ellipsoids at 50% probability.
Figure 1. The asymmetric unit of 1 with atom numbering; ellipsoids at 50% probability.
Crystals 09 00045 g001
Crystals 09 00045 g002 550
Figure 2. Projection of structures of 1·5H2O and 1 along (a–c) crystallographic directions.
Figure 2. Projection of structures of 1·5H2O and 1 along (a–c) crystallographic directions.
Crystals 09 00045 g002
Crystals 09 00045 g003 550
Figure 3. Structure of 2·3H2O with atom numbering; ellipsoids at 50% probability.
Figure 3. Structure of 2·3H2O with atom numbering; ellipsoids at 50% probability.
Crystals 09 00045 g003
Crystals 09 00045 g004 550
Figure 4. Projection of the structure of 2·3H2O along (a,b) crystallographic directions; symmetrically independent molecules marked pink and violet.
Figure 4. Projection of the structure of 2·3H2O along (a,b) crystallographic directions; symmetrically independent molecules marked pink and violet.
Crystals 09 00045 g004
Crystals 09 00045 g005 550
Figure 5. Temperature dependence of the DC magnetic susceptibility at 1000 Oe for 1·5H2O, 1 and 2·3H2O.
Figure 5. Temperature dependence of the DC magnetic susceptibility at 1000 Oe for 1·5H2O, 1 and 2·3H2O.
Crystals 09 00045 g005
Crystals 09 00045 g006 550
Figure 6. Field dependence of magnetization at 1.8 K for 1·5H2O, 1 and 2·3H2O.
Figure 6. Field dependence of magnetization at 1.8 K for 1·5H2O, 1 and 2·3H2O.
Crystals 09 00045 g006
Table
Table 1. Structure and refinement data for 1 and 2·3H2O; data for 1·5H2O included for comparison.
Table 1. Structure and refinement data for 1 and 2·3H2O; data for 1·5H2O included for comparison.
1·5H2O 112·3H2O
Empirical formulaC46H82Cu3N28O5W2C46H72Cu3N28W2C46H82Cu3N28O5W2
Formula weight1665.721575.571665.72
Crystal systemtriclinictriclinicmonoclinic
Space groupP −1P −1P 21/n
a [Å]8.9255(11)9.0228(5)14.0566(7)
b [Å]10.0938(13)10.8399(8)12.8685(7)
c [Å]19.549(3)17.8734(13)36.7198(19)
α [°]78.342(5)75.409(6)90.0
β [°]83.074(5)87.810(4)100.821(2)
γ [°]69.472(5)60.092(7)90.0
V [Å3]1613.0(4)1458.5(8)6524.0(3)
Z114
dc [g·cm−3]1.7151.7941.696
µ [mm−1]4.5905.0644.539
F(000)8297793276
θ range [°]1.07–28.282.79–25.42.37–29.15
Reflns collected21,0645 26117,526
No. of params380356746
Rint0.06930.05320.0362
GooF (F2)-1.0181.059
R1 [I > 2σ(I)]0.06930.07080.0446
ωR2 (all data)0.16620.15100.0973
1 Data from reference [22].
Table
Table 2. Selected bond lengths (Å) and angles (°) in 1·5H2O and 1.
Table 2. Selected bond lengths (Å) and angles (°) in 1·5H2O and 1.
Bond1·5H2O 11Angle1·5H2O 11
W1-C12.1812.149Cu1-N1-C1143.0129.3
W1-C22.1572.129Cu1-N4-C4157.1135.3
W1-C32.1542.159Cu2-N5-C5157.1142.1
W1-C42.1692.155N11-Cu1-N1293.2286.1
W1-C52.1652.152N12-Cu1-N1386.4495.5
W1-C62.1522.159N13-Cu1-N1494.2386.6
W1-C72.1582.149N14-Cu1-N1185.9391.9
W1-C82.1692.214N21-Cu2-N2286.3486.2
Cu1-N12.6982.606W1-C1-N1176.75176.3
Cu1-N42.5102.585W1-C4-N4177.74179.4
Cu2-N52.5562.503W1-C5-N5174.43176.5
Cu1-N112.0042.037
Cu1-N122.0232.027
Cu1-N132.0242.018
Cu1-N142.0141.998
Cu2-N212.0152.011
Cu2-N222.0322.028
1 Data from reference [22].
Table
Table 3. Selected bond lengths (Å) and angles (°) in 2·3H2O.
Table 3. Selected bond lengths (Å) and angles (°) in 2·3H2O.
Cu1-N112.523Cu1-N11-C11157.9
Cu1-O12.518Cu2-N13-C13137.2
Cu2-N132.596Cu3-N21-C21153.9
Cu3-N212.594Cu4-N23-C23142.8
Cu3-O22.422N101-Cu1-N10293.3
Cu4-N232.457N102-Cu1-N10386.0
Cu1-N1012.013N103-Cu1-N10495.0
Cu1-N1022.037N104-Cu1-N10185.7
Cu1-N1032.011N201-Cu2-N20286.0
Cu1-N1042.023N301-Cu3-N30285.8
Cu2-N2012.008N302-Cu3-N30392.8
Cu2-N2022.019N303-Cu3-N30486.4
Cu3-N3012.021N304-Cu3-N30195.0
Cu3-N3022.029N401-Cu4-N40285.6
Cu3-N3032.008W1-C11-N11178.5
Cu3-N3042.013W1-C13-N13177.2
Cu4-N4012.024W2-C21-N21179.6
Cu4-N4022.016W2-C23-N23176.5

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Pacanowska, A.; Reczyński, M.; Nowicka, B. Modification of Structure and Magnetic Properties in Coordination Assemblies Based on [Cu(cyclam)]2+ and [W(CN)8]3−. Crystals 2019, 9, 45. https://doi.org/10.3390/cryst9010045

AMA Style

Pacanowska A, Reczyński M, Nowicka B. Modification of Structure and Magnetic Properties in Coordination Assemblies Based on [Cu(cyclam)]2+ and [W(CN)8]3−. Crystals. 2019; 9(1):45. https://doi.org/10.3390/cryst9010045

Chicago/Turabian Style

Pacanowska, Aleksandra, Mateusz Reczyński, and Beata Nowicka. 2019. "Modification of Structure and Magnetic Properties in Coordination Assemblies Based on [Cu(cyclam)]2+ and [W(CN)8]3−" Crystals 9, no. 1: 45. https://doi.org/10.3390/cryst9010045

APA Style

Pacanowska, A., Reczyński, M., & Nowicka, B. (2019). Modification of Structure and Magnetic Properties in Coordination Assemblies Based on [Cu(cyclam)]2+ and [W(CN)8]3−. Crystals, 9(1), 45. https://doi.org/10.3390/cryst9010045

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