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Crystals 2014, 4(2), 104-112; doi:10.3390/cryst4020104
Published: 15 May 2014
Abstract: Iron(III) compounds with long alkyl chains, [Fe(Cn-pap)2]ClO4 (Cn-pap: alkoxy-2-(2-pyridylmethyleneamino)phenol, n = 8 (1), 10 (2), 12 (3), 14 (4), 16 (5)) have been synthesized. The compounds were characterized by single crystal X-ray structure analysis and temperature dependent magnetic susceptibility in order to research the relationship between magnetic properties and the presence of long alkyl chains in soft molecules of the present type. The compounds 1, 2, 3 and 4 are in the high-spin (HS) state over the temperature range of 5 to 400 K. On the other hand, compound 5 is low-spin (LS) showing that the difference in magnetic properties depends on the length of the alkyl chain in the respective compounds.
Metal proteins and enzymes consist of flexible structures typified by peptide links surrounding active centers giving rise to “flexible space” which may play an important role in the biochemical function of such systems . In soft materials such as liquid crystals, gels and polymers, the presence of “flexible space” can be an important influence controlling the properties of such materials [2,3,4,5,6,7,8,9,10]. This motivated us to construct metal complexes with attached long alkyl chains that would result in flexible space in conjunction with the presence of metal complex centers. Positioning a spin-crossover (SCO) metal complex within the flexible space formed by the long alkyl chains is expected to result in altered properties based on synergic interactions occurring between the SCO and its environment reflecting external stimuli. A variety of dn (n = 4–7) transition metal compounds exhibiting SCO between the high-spin (HS) and low-spin (LS) states have been reported . Gradual or abrupt SCO may be observed in the solid state, depending on the degree of intermolecular cooperativity present. Flexibility in molecular assemblies based on molecular units has been shown to be an important factor in achieving synergy and resulting in various interesting physical properties among advanced materials [2,3,4,5,6,7,8,9,10].
Generally, SCO iron(III) compounds exhibit a 1/2 ↔ 5/2 spin change. It has been known that the iron(III) compounds [Fe(pap)2]X·H2O (Hpap = 2-(2-pyridylmethyleneamino)phenol, X = BF4− or ClO4−) exhibit abrupt SCO behavior [11,12,13,14,15]. We suggested that the strong intermolecular interactions (π–π stacking, hydrogen bonding and so on) are important for cooperativity. Although the π-conjugated system clearly plays an important role, in some cases the presence of long alkyl chains may also influence the magnetic behavior through intermolecular interaction. We have attempted to add long alkyl chains to iron(III) compounds with pap ligands. In this paper, we report about the iron(III) compounds [Fe(Cn-pap)2]ClO4 (n = 8 (1), 10 (2), 12 (3), 14 (4), 16 (5)).
2. Results and Discussion
The compounds 1–5 were prepared and characterized by elemental analysis. Single crystals of 4 suitable for X-ray structural analysis were obtained by slow recrystallization of the initial product from MeOH:CHCl3 (1:1). Single-crystal X-ray analysis of 4 was successfully carried out at 143 K (Figure 1) . An ORTEP view of compound 4 is shown in Figure 1a. X-ray crystallographic data for 4 are given in Table 1. Complex 4 crystallizes in the space group P-1. The iron(III) ions are octahedrally coordinated by four nitrogen atoms and two oxygen atoms from two C14-pap ligands, i.e., an N4O2 donor set. The Fe–N distances, the Fe–O distances, the N–Fe–N angles, the N–Fe–O angles and the O–Fe–O angles for 4 are shown in Table 1. The Fe(1)–N(1) and Fe(1)–N(3) axial bond distances, 2.109(2) and 2.112(2) Å, are shorter than the Fe(1)–N(2) and Fe(1)–N(4) distances, 2.207(2) and 2.2213(17) Å. The Fe(1)–O(1) and Fe(1)–O(3) bond distances, 1.935(1) and 1.9364(16) Å are the shortest because of their ionic character. These bond lengths are typical for HS iron(III) compounds. The N–Fe–N angles and the N–Fe–O angles are N(1)–Fe(1)–N(3) = 167.26(6)°, N(2)–Fe(1)–O(1) = 152.76(8)° N(4)–Fe(1)–O(3) = 152.42(7)°, respectively, indicating that the [FeN4O2] octahedron core is distorted. Compound 4 forms an angled Z-shaped structure with the two coordinated C14-pap donor fragments nearly perpendicular to one another. A view of the packing for 4 is shown in Figure 1b. It shows that the arrangement of the long alkyl chains is not affected by the ClO4− counter ions. There are two strong intermolecular interactions between each molecule. One is a π–π interaction between pap ligands, and the second is a “fastener” effect between the long alkyl chains which align adjacent to each other in the lattice.
The temperature dependences of the magnetic susceptibility for the compounds 1–5 were measured in the form of the χmT versus T curve, where χm is the molar magnetic susceptibility and T is the temperature (Figure 2). The compounds 1–4 are in the HS state in the temperature range of 5–400 K. The χmT value for 1 increased abruptly from 1.64 cm3·Kmol−1 at 5 K to 3.00 cm3n·Kmol−1 at 65 K and increased gradually to 3.89 cm3·Kmol−1 at 400 K. The value at 400 K is smaller than that in iron(III) HS (4.38 cm3·Kmol−1), and it is proposed that an LS specie is mixed even at 400 K. The χmT value for 2 increased abruptly from 3.32 cm3·Kmol−1 at 5 K to 4.16 cm3·Kmol−1 at 24 K and increased gradually to 4.69 cm3·Kmol−1 at 400 K. The χmT value for 3 increased abruptly from 2.54 cm3·Kmol−1 at 5 K to 3.39 cm3·Kmol−1 at 27 K and increased gradually to 4.00 cm3·Kmol−1 at 400 K. The value also indicates the mixture of a small amount of LS specie. The χmT value for 4 increased abruptly from 4.01 cm3·Kmol−1 at 5 K to 5.55 cm3·Kmol−1 at 41 K and decreased gradually to 4.21 cm3·Kmol−1 at 400 K. Compound 4 shows weak ferromagnetic interactions between the complexes, it is proposed that the ferromagnetic interaction results from interchain interactions. Furthermore, the decrease in the χmT value below 50 K is due to zero field splitting. On the other hand, the χmT value for 5 increased gradually from 0.57 cm3·Kmol−1 at 5 K to 1.32 cm3·Kmol−1 at 400 K, in accord with compound 5 being in the LS state at room temperature. This compound has the longest alkyl chain (C16), and hence the strongest interchain interaction can be expected, in accord with it adopting the LS state.
|Table 1. Crystal parameter, and bond lengths and angles for compound 4.|
|Compound||4||Metal-ligand Ligand-metal-ligand||Bond lengths (Å) and angles (°)|
|CCDC Number ||988486||Fe–N(1)||2.109|
|Crystal size/mm3||0.200 × 0.180 × 0.020||Fe–N(4)||2.221|
|Space group||P-1 (#2)||Fe–O(3)||1.936|
|h, k, l range||−13 ≤ h ≤ 13||N(2)–Fe–N(3)||103.26(8)|
|−15 ≤ k ≤ 15||N(2)–Fe–N(4)||93.37(8)|
|−28 ≤ l ≤ 28||N(3)–Fe–N(4)||73.90(7)|
|Independent reflections (Rint)||11,396 (0.0499)||–||–|
|Observed reflections [I ≥ 2σ(I)]||9,058||–||–|
|R1/wR2 [I ≥ 2σ(I)]||0.0685/0.1811||–||–|
|R1/wR2 (all data)||0.0847/0.1811||–||–|
3. Experimental Section
All reagents were obtained commercially (Wako, Kumamoto, Japan) and were used in the form that they were received. The reactions were performed under N2.
3.1. Synthesis of 5-Hydroxy-2-Methylpyridine N-Oxide
A solution of 5-hydroxy-2-methylpyridine (7.50 g, 0.70 mol, 1 eq.) and hydrogen peroxide 30% (16.5 mL, q.s.) in CH3COOH (150 mL) was heated at 80 °C for 2.5 h. A solution color change was observed from orange to pale yellow. The solution was further stirred at room temperature for 24 h and concentrated in vacuo. Acetone was added to force precipitation. The resulting pale yellow precipitate was collected by vacuum filtration (6.60 g, 77%). 1H-NMR (CD3OD): 7.93 (d 1H) 7.32 (d 1H) 7.03 (dd 1H) 2.41 (s 3H).
3.2. Synthesis of 2-Pyridylmethanol Acetate
5-Hydroxy-2-methylpyridine N-oxide (6.60 g, 0.05 mol, 1 eq.) was added slowly to (CH3CO)2O (65 mL) at 110 °C. The resultant dark brown reaction mixture was stirred for 2 h at 140 °C. EtOH (150 mL) was added and the solution was concentrated in vacuo to yield a brown oil. CHCl3 (40 mL) was added and the solution was neutralized with saturated NaHCO3. The organic layer was collected and washed with saturated NaHCO3 (30 mL × 2), dried (MgSO4, q.s.) and filtered. The solvent was removed in vacuo to yield a brown oil, which was further dried under high vacuum for 2 h. Without purification the product was used for next reaction. 1H-NMR (CDCl3): 8.40 (d 1H) 7.49 (d 1H) 7.39 (dd 1H) 5.21 (s 2H) 2.33 (s 3H) 2.15 (s 3H).
3.3. Synthesis of 5-Hydroxy-2-Hydroxymethylpyridine
A solution of 2-pyridylmethanol acetate (q.s.) in conc. HCl (10 mL) was heated under reflux for 1.5 h. The reaction mixture was cooled to room temperature and concentrated in vacuo. CHCl3 (40 mL) was added and the solution neutralized carefully with saturated NaHCO3. The aqueous layers were collected through washings with saturated NaHCO3 and concentrated in vacuo. The brown solid was triturated with MeOH and filtrates collected through filtration. The solvent was removed in vacuo yielding a brown solid (3.20 g). 1H-NMR (CDCl3): 7.85 (d 1H) 7.18 (d 1H) 7.01 (dd 1H) 4.51 (s 2H).
3.4. Synthesis of 5-Hydroxypyridine 2-Carbaldehyde
A suspension of 5-hydroxy-2-hydroxymethylpyridine (3.20 g, 0.03 mol) and MnO2 (oven dried, q.s.) in iso-PrOH (100 mL) was heated under reflux for 24 h. The hot mixture was filtered through Celite® and washed thoroughly with hot MeOH (q.s.). The solution was allowed to cool to room temperature and concentrated in vacuo, yielding a brown solid. The solid was purified by chromatography on a short silica gel column (gradient elution; 0% to 5% methanol in CH2Cl2). The solvent was removed in vacuo to yield a brown solid (0.96 g, 26%). 1H-NMR (CD3OD): 9.60 (s 1H) 7.90 (d 1H) 7.74 (d 1H) 6.84 (dd 1H).
3.5. Synthesis of 5-(n-alkoxy)Pyridine 2-Carbaldehyde (n = 8, 10, 12, 14, 16)
5-Hydroxypyridine-2-carbaldehyde (3.30 mmol, 1 eq.), K2CO3 (3.30 mmol, 1 eq) and n-alkylbromide (3.50 mmol, n = 8–16) were stirred vigorously in dry DMF at 100 °C for 6 h. After cooling to room temperature, the solvent was removed in vacuo. The solid was purified by chromatography on a short silica gel column (hexane:ethyl acetate = 5:1). The solvent was removed in vacuo to yield a white solid.
3.6. Synthesis of Cn-pap (n = 8, 10, 12, 14, 16) (L1)–(L5)
5-(n-Alkoxy)pyridine-2-carbaldehyde (1 eq) and 2-aminophenol (1 eq) were stirred in MeOH. A solution color change from yellow to orange was observed. The solution was concentrated in vacuo and left in a refrigerator for several hours. The precipitate was collected by vacuum filtration.
1H-NMR (500 MHz; CDCl3): L1; 8.85 (s, 1H, pyH), 8.20 (s, 1H, pyH), 7.61 (d, 1H, pyH) 7.49 (m, 1H, N–CH2), 7.14 (m, 2H, ArH), 6.78 (m, 2H, ArH), 4.88 (s, 1H, OH), 3.95 (m, 2H, CH2 of main chain), 1.73 (m, 2H, CH2 of main chain), 1.33 (m, 2H, CH2 of main chain), 1.25 (s, 8H, CH2 of main chain), 0.95 (s, 3H, CH3), L2; 8.79 (s, 1H, pyH), 8.21 (s, 1H, pyH), 7.59 (d, 1H, pyH) 7.40 (m, 1H, N–CH2), 7.12 (m, 2H, ArH), 6.75 (m, 2H, ArH), 4.90 (s, 1H, OH), 3.92 (m, 2H, CH2 of main chain), 1.73 (m, 2H, CH2 of main chain), 1.30 (m, 2H, CH2 of main chain), 1.20 (s, 12H, CH2 of main chain), 0.92 (s, 3H, CH3), L3; 8.81 (s, 1H, pyH), 8.22 (s, 1H, pyH), 7.59 (d, 1H, pyH) 7.47 (m, 1H, N–CH2), 7.11 (m, 2H, ArH), 6.75 (m, 2H, ArH), 4.85 (s, 1H, OH), 3.99 (m, 2H, CH2 of main chain), 1.70 (m, 2H, CH2 of main chain), 1.35 (m, 2H, CH2 of main chain), 1.25 (s, 16H, CH2 of main chain), 0.93 (s, 3H, CH3), L4; 8.84 (s, 1H, pyH), 8.19 (s, 1H, pyH), 7.63 (d, 1H, pyH) 7.45 (m, 1H, N–CH2), 7.14 (m, 2H, ArH), 6.80 (m, 2H, ArH), 5.01 (s, 1H, OH), 3.94 (m, 2H, CH2 of main chain), 1.75 (m, 2H, CH2 of main chain), 1.35 (m, 2H, CH2 of main chain), 1.24 (s, 20H, CH2 of main chain), 0.96 (s, 3H, CH3), L5; 8.80 (s, 1H, pyH), 8.18 (s, 1H, pyH), 7.58 (d, 1H, pyH) 7.44 (m, 1H, N–CH2), 7.10 (m, 2H, ArH), 6.88 (m, 2H, ArH), 4.85 (s, 1H, OH), 3.91 (m, 2H, CH2 of main chain), 1.77 (m, 2H, CH2 of main chain), 1.36 (m, 2H, CH2 of main chain), 1.27 (s, 24H, CH2 of main chain), 0.90 (s, 3H, CH3).
3.7. Synthesis of [Fe(Cn-pap)2]ClO4 (n = 8, 10, 12, 14, 16) (1)–(5)
Cn-pap (2 eq) was dissolved in CHCl3 and Fe(ClO4)3·nH2O (1.5 eq) in MeOH (10 mL) was added to the solution. The solution was stirred and then concentrated. The microcrystals of product that formed were collected by filtration and recrystallized from MeOH/CHCl3.
The composition of the bulk materials were confirmed through elemental analyses. [Fe(C8-pap)2]ClO4 (1), Anal. Calcd. for C40H50O8N4Cl1Fe1: C, 59.60; H, 6.25; N, 6.95. Found: C, 59.76; H, 6.38; N, 6.85. [Fe(C10-pap)2]ClO4 (2), Anal. Calcd. for C44H58O8N4Cl1Fe1: C, 61.29; H, 6.78; N, 6.50. Found: C, 61.13; H, 6.73; N, 6.08. [Fe(C12-pap)2]ClO4 (3), Anal. Calcd. for C48H66O8N4Cl1Fe1: C, 62.78; H, 7.24; N, 6.10. Found: C, 62.62; H, 7.53; N, 6.27. [Fe(C14-pap)2]ClO4 (4), Anal. Calcd. for C52H74O8N4Cl1Fe1: C, 64.09; H, 7.65; N, 5.75. Found: C, 64.02; H, 7.53; N, 5.87. [Fe(C16-pap)2]ClO4 (5), Anal. Calcd. for C56H82O8N4Cl1Fe1: C, 65.26; H, 8.02; N, 5.44. Found: C, 65.62; H, 8.13; N, 5.47.
The magnetic properties were determined by temperature-dependent susceptibility measurement with a Superconducting Quantum Interference Device (SQUID) magnetometer at field strengths of 1 T.
[Fe(Cn-pap)2]ClO4 (n = 8, 10, 12, 14, 16) have been synthesized and characterized. The single crystal X-ray analysis for compound 4 showed that there is fastener effect between long alkyl chains of neighboring molecules. The compounds 1–4 are in the HS states and compound 5 is in the LS state. Furthermore 4 shows weak ferromagnetic interaction between individual complexes in accord with the presence of a cooperative interaction being an important factor for inducing such a magnetic interaction.
This work was supported by Innovative Areas “Coordination Programming” (Area 2107), “Science of Atomic Layers” (Area 2506) and Grant-in-Aids for Science Research (No. 26288026) from the Ministry of Education, Culture, Sports, Science and Technology of the Japanese Government.
Manabu Nakaya, Saliu Alao Amolegbe, Masaaki Nakamura, and Shinya Hayami conceived the project. Manabu Nakaya, Saliu Alao Amolegbe, Masaaki Nakamura, Kodai Shimayama, Kohei Takami, Kazuya Hirata and Shinya Hayami designed the experiments. Manabu Nakaya and Kodai Shimayama performed all synthesis and characterisation experiments. Manabu Nakaya, Leonald F. Lindoy and Shinya Hayami analysed the data and co-wrote the manuscript. All authors discussed the results and commented on the manuscript.
Conflicts of Interest
The authors declare no conflict of interest.
References and Notes
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- Crystal data for 4 at 143 K: fw = 974.48; colorless prism, crystal dimensions of 0.200 mm × 0.180 mm × 0.020 mm, triclinic, space group P-1; a = 10.6395(10) Å, b = 12.2937(10) Å, c = 22.129(3) Å, α = 74.026(9)°, β = 84.735(11)°, γ = 65.255(9)°, V = 2526.2(5) Å3, Z = 2, Dcalc = 1.281 g·cm−3, R1 = 0.0685 for I > 2σ(I), R = 0.049 and Rw = 0.181 for all data with a linear absorption coefficient μ(Mo Kα) = 4.073 cm−1.
- CCDC 988486 contains 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 (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: +44 1223 336033; E-mail: email@example.com).
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