Increasing the operating temperatures of single-molecule magnets—molecules that can retain magnetic polarization in the absence of an applied field—has potential implications toward information storage and computing, and may also inform the development of new bulk magnets. Progress toward these goals relies upon the development of synthetic chemistry enabling enhancement of the thermal barrier to reversal of the magnetic moment, while suppressing alternative relaxation processes. Herein, we show that pairing the axial magnetic anisotropy enforced by tetramethylcyclopentadienyl (CpMe4H) capping ligands with strong magnetic exchange coupling provided by an N23− radical bridging ligand results in a series of dilanthanide complexes exhibiting exceptionally large magnetic hysteresis loops that persist to high temperatures. Significantly, reducing the coordination number of the metal centers appears to increase axial magnetic anisotropy, giving rise to larger magnetic relaxation barriers and 100-s magnetic blocking temperatures of up to 20 K, as observed for the complex [K(crypt-222)][(CpMe4H2Tb)2(μ−)].
Single-molecule magnets are molecules in which a strong axial anisotropy, imparted by the ligand field surrounding one or more metal centers, acts to create a bistable ground state, for which an activation barrier U must be overcome to reverse the orientation of the magnetic moment. The potential application of such species in high-density information storage1, as well as quantum computing2 and spin-based electronics3, hinges upon improving not just the defining thermal energy barrier to magnetization reversal, but also the magnetic blocking temperature and coercive field—metrics that determine the ability of the molecules to retain information upon removal of an applied magnetic field 4. The use of selected 4f metal ions, particularly TbIII, DyIII, and ErIII, has recently dominated this area of research due to the advantageous combination of high magnetic moment and intrinsic magnetic anisotropy engendered by large spin–orbit coupling4,5,6,7,8,9,10,11. Progress in increasing blocking temperatures and coercive fields has been challenging mainly owing to the prevalence of through-barrier relaxation pathways, such as quantum tunneling of the magnetization, though recent reports on a molecule containing a single DyIII ion demonstrate Orbach relaxation proceeding through nearly the entire effective magnetization reversal barrier (Ueff) of greater than 1200 cm−1, with a correspondingly high 100-s blocking temperature12, 13.
Coordination chemistry can be utilized to yield electronic structures designed to prevent through-barrier relaxation pathways, with the goal of attaining magnetic blocking temperatures that scale with the magnitude of Ueff14. One strategy for suppressing quantum tunneling of the magnetization is to establish rigorously symmetry-protected pure MJ states15, a condition as-yet only experimentally achieved in adatom-surface experiments16, though reports of the high-blocking temperature [Dy(Cpttt)2]+ (Cpttt = 1,2,4-tri(tert-butyl)cyclopentadienide) complex suggest that rigorous symmetry may not be crucial to achieve high performance in single-ion magnetic molecules12, 13. Another promising route is the design of systems with strong intramolecular magnetic coupling between two or more metal centers. In addition to creating a more classical coupled system with large total angular momentum, magnetic coupling has been postulated to generate an exchange bias field that impedes quantum tunneling of the magnetization17,18,19,20. In recent years, a particularly successful strategy to promote strong magnetic coupling between lanthanide centers has been the employment of paramagnetic bridging ligands21,22,23,24,25,26,27,28. Significantly, the diffuse spin orbitals of anionic radical ligands are better able to penetrate into the core electron density of the deeply buried 4f orbitals. Our strategy toward high-performance single-molecule magnets therefore targets systems in which radical ligands facilitate a direct exchange coupling with lanthanide ions constrained in coordination environments that promote strong axial magnetic anisotropy. Here we show that this can be achieved in two new series of organometallic N23− radical-bridged dilanthanide complex salts: [K(crypt-222)(THF)][(CpMe4H2Ln(THF))2(μ−)] (crypt-222 = 2.2.2-cryptand, THF = tetrahydrofuran, CpMe4H = tetramethylcyclopentadienyl, Ln = Gd (1-Gd), Tb (1-Tb), Dy (1-Dy)) and [K(crypt-222)][(CpMe4H2Ln)2(μ−)], (Ln = Tb (2-Tb), Dy (2-Dy)). Notably, 2-Tb exhibits the highest coercive field yet observed for any molecular magnet, substantially larger even than those of commercial permanent magnets, as well as the highest 100-s blocking temperature for a terbium single-molecule magnet.
Synthesis and structural studies
The dilanthanide precursor complexes (CpMe4H2Ln(THF))2(µ-N2) (Ln = Gd (3-Gd), Tb (3-Tb), Dy (3-Dy)) are readily obtained via treatment of CpMe4H2Ln(BPh4) with KC8, which prompts the reduction of dinitrogen29, 30. Subsequent syntheses of compounds of type 1-Ln employ KC8 in the presence of 2.2.2-cryptand in THF to reduce the N22−-bridged molecules of 3-Ln (Fig. 1). The first series of radical-bridged complex salts then comprises the isostructural compounds 1-Gd, 1-Tb, and 1-Dy, which feature two crystallographically inequivalent lanthanide centers that are each ligated by two tetramethylcyclopentadienyl rings, one THF molecule, and a radical N23− bridging ligand that is coordinated in a side-on fashion (Fig. 1 and Supplementary Figs. 1 and 2). The THF ligands in compounds 1-Tb and 1-Dy can be readily dissociated by dissolution in 2-methyltetrahydrofuran (2-MeTHF), with the more sterically encumbered donor solvent enabling 2-Tb and 2-Dy to be crystallized from concentrated solutions. The isostructural compounds 2-Tb and 2-Dy are THF-free, resulting in decreased metal coordination numbers and increased Ln–N23−–Ln dihedral angles of 178.5(2)° and 178.9(3)°, compared to 173.45(16)° and 173.14(8)° in 1-Tb and 1-Dy, respectively (Fig. 1 and Supplementary Fig. 3). The analogous reaction with 1-Gd instead affords [K(crypt-222)][(CpMe4H2Gd(2-MeTHF))2(μ−)] (4), wherein the coordination of 2-MeTHF is a consequence of the larger radius of the GdIII ion (Supplementary Fig. 4).
Magnetic susceptibility measurements
Magnetic exchange coupling in the new compounds was first probed through measurement of the temperature dependence of the product of magnetic susceptibility and temperature (χMT). Complex 1-Gd exhibits a room temperature χMT value of 15.3 emu·K/mol, somewhat lower than the value of 16.13 emu·K/mol expected for two magnetically isolated S = 7/2 GdIII centers and an S = 1/2 radical spin. With decreasing temperature, a distinct rise in χMT is observed, up to a maximum value of 20.4 emu·K/mol at 10 K, owing to the presence of antiferromagnetic gadolinium-radical coupling which creates an S = 13/2 ground state that becomes isolated at low temperature. The magnetic coupling strength for 1-Gd could be quantified using the spin-only Hamiltonian Ĥ = −2JGd–radŜrad·(ŜGd(1) + ŜGd(2)), which reveals a Gd–N23− coupling constant of JGd–rad = –20 cm−1 (Fig. 2 and Supplementary Figs. 5, 6 and 7). This represents the second largest coupling constant yet observed for a gadolinium-containing compound, following that of a similar N23−-bridged complex with JGd–rad = –27 cm−121, and is significantly greater than the JGd–rad of –11 cm−1 observed for both a mononuclear gadolinium–nitronyl nitroxide radical complex31 and an indigo radical-bridged digadolinium complex28. Such strong antiferromagnetic coupling reflects the diffuse character of the radical spin of the compact, highly anionic N23− bridging unit, which is localized in the π* orbital perpendicular to the Ln2(µ−η2:η2−N2) plane32.
Compounds 1-Dy, 1-Tb, 2-Dy, and 2-Tb exhibit similar increases in χMT with decreasing temperature, which are attributed to the presence of strongly coupled, higher-angular momentum ground states. Room temperature χMT values of 28.0 (1-Dy), 25.1 (1-Tb), 28.1 (2-Dy), and 24.2 (2-Tb) emu·K/mol are observed under an applied field of 1 T. The χMT values expected for magnetically isolated DyIII2–N23− and TbIII2–N23− complexes are 28.7 and 24.0 emu·K/mol, respectively. The observed values then increase to local maxima of 38.6 emu·K/mol at 40 K (1-Dy), 36.5 emu·K/mol at 65 K (1-Tb), 41.8 emu·K/mol at 32 K (2-Dy), and 32.6 emu·K/mol at 75 K (2-Tb) (Fig. 2 and Supplementary Figs. 5–25). Such dramatic increases in χMT again indicate strong coupling between the lanthanide centers and the N23− radical ligand, where the higher temperature of the maxima of 1-Tb and 2-Tb compared to those of 1-Dy and 2-Dy additionally suggest that the Ln–N23− coupling is stronger in the terbium congeners. While a subsequent decline in χMT with further decreasing temperature could be attributed to depopulation of Zeeman-split, coupled M J states, the sudden, steep plummet observed for these complexes more likely signifies magnetic blocking due to a pinning of the moment along the easy axis within the immobilized crystallites at low temperatures. Indeed, magnetic blocking behavior is confirmed by the sharp divergence of the field-cooled and zero-field-cooled magnetic susceptibility data collected at 1 T, which occurs at 14.5 K for 1-Tb, 7.5 K for 2-Dy, and 20 K for 2-Tb (Fig. 2 and Supplementary Figs. 26 and 27).
Variable-frequency, variable-temperature in-phase (χM′) and out-of-phase (χM″) ac magnetic susceptibility data were collected in order to probe whether the magnetic blocking arises from single-molecule magnet behavior (Fig. 3 and Supplementary Figs. 28–49). Peaks were indeed observed in χM″ for 1-Dy, 1-Tb, 2-Dy, and 2-Tb, indicative of slow magnetic relaxation. Magnetic relaxation times, τ, were extracted from fitting plots of χM″ vs. χM′ using a generalized Debye equation, and were then used to construct Arrhenius plots (Fig. 4 and Supplementary Fig. 49). These plots enable analysis of the temperature dependence of the magnetic relaxation times, which yields detailed insights into what magnetic relaxation pathways are operational. In particular, a thermally activated Orbach process shows an exponential dependence of τ upon temperature, while a quantum tunneling process is temperature independent. The various types of relaxation pathways observed reveal key correlations between structure and magnetic relaxation behavior in lanthanide–radical molecular magnets. Moreover, the magnetic blocking temperature, Tb, for a single-molecule magnet is best evaluated using such relaxation time data, which, unlike hysteresis or field-cooled/zero-field-cooled measurements, are not sweep rate dependent. In particular, the temperature associated with a magnetic relaxation time of 100 s has been suggested as the standard for comparison of single-molecule magnets33.
The relaxation time data for 1-Dy were fit using two relaxation processes, an Orbach process, and a quantum tunneling process to yield a thermal relaxation barrier of Ueff = 110(1) cm−1, together with a relaxation attempt time of τ0 = 3.1(1) × 10−9 s (Fig. 4b, Supplementary Figs. 28–32, and Supplementary Table 1). The presence of quantum tunneling typically precludes magnetic blocking. Consequently, 1-Dy exhibits substantially waist-restricted hysteresis loops even at 2 K, at which temperature the complex achieves a maximum magnetic relaxation time of just 0.41 s (Supplementary Fig. 33). In contrast, the thermally activated relaxation regime, in which the relaxation time increases exponentially as the temperature is lowered, persists over the entire range of temperatures accessible in the ac susceptibility measurements for 1-Tb and 2-Dy, yielding effective spin-reversal barriers, Ueff, of 242(2) and 108.1(2) cm−1, respectively (Supplementary Figs. 34–45, and Supplementary Tables 2 and 3). Variable-field magnetization measurements on the latter two complexes reveal wide magnetic hysteresis loops with no evidence of tunneling, and 100-s magnetic blocking temperatures of 14 and 6.6 K, respectively, were determined from dc relaxation measurements (Figs. 4 and 5 and Supplementary Figs. 38 and 44).
The prevalence of quantum tunneling for 1-Dy likely can be ascribed to a reduction in the axiality of the DyIII ground states due to THF coordination. Indeed, this explanation is supported by the enhanced relaxation times and wide magnetic hysteresis exhibited by 2-Dy below 7.5 K (Fig. 5b), in conjunction with the removal of coordinated THF and enhanced axial symmetry.
In the case of 1-Tb, the substantially stronger exchange coupling with the radical N23− ligand, first noted in the relatively high-temperature maximum in χMT, coincides with relaxation times as long as 1.11 h and wide magnetic hysteresis, in spite of the presence of coordinated THF. This result suggests that an enhancement of axial anisotropy of the TbIII ions in 2-Tb via loss of coordinated THF should further improve upon this outstanding slow magnetic relaxation behavior, in analogy to the improvement in the magnetic behavior of 2-Dy relative to 1-Dy.
Magnetic relaxation time data for 2-Tb were collected over an extended temperature range of 2–60 K using dc relaxation and high-frequency ac susceptibility techniques (Fig. 4c, Supplementary Figs. 46–56, and Supplementary Table 4). The data reveal relaxation times as long as 12.6 h at low temperatures, and, significantly, a deviation from linearity at the highest temperatures probed. Consequently, fitting the data required implementation of not just one, but two Orbach processes in addition to a quantum tunneling term, yielding relaxation barriers of Ueff,1 = 276(1) cm-1 and Ueff,2 = 564(17) cm−1. The first barrier of 276 cm−1 represents to the best of our knowledge the highest value yet observed for a radical-bridged single-molecule magnet, followed by barriers of Ueff = 242 cm−1 for 1-Tb and Ueff = 227 cm−1 for [(((Me3Si)2N)2Tb(THF))2(μ−)]−22. Consistent with this activation barrier, the 100-s blocking temperature for 2-Tb is measured to be 20 K, setting a record for both terbium-based and multinuclear single-molecule magnets. Dramatic improvements in magnetic behavior for 2-Tb and 2-Dy compared to 1-Tb and 1-Dy appear to reflect a reduction in transverse anisotropy of the LnIII ions, although an additional factor may be the increase in planarity of the Ln2N2 unit upon removal of THF. This reduction in transverse anisotropy appears to facilitate an unperturbed, strong antiferromagnetic lanthanide–radical coupling for 2-Tb and 2-Dy, while also likely suppressing unfavorable antiferromagnetic lanthanide–lanthanide interactions34. Together, a reduction of both transverse anisotropy and detrimental exchange coupling pathways should increase not only the axiality of the ground state, but also that of exchange-coupled excited states, possibly enabling observation of magnetic relaxation through excited states20, 35.
With this in mind, one point of note regarding the two thermal activation barriers to reversal of magnetization observed for 2-Tb is that the Ueff,2 barrier of 564 cm−1 is close to double that of the Ueff,1 barrier of 276 cm−1. These results may thus constitute the first evidence of magnetic relaxation through a “spin ladder” for a lanthanide–radical single-molecule magnet, in which the energy of each rung is determined by a multiple of 2JLn–rad (Supplementary Fig. 57). Computational studies of N23−-bridged complexes have suggested that if crystal field splitting of the LnIII ions is sufficiently high compared to the magnitude of exchange coupling, mixing of exchange- and crystal field-split doublets is reduced, promoting axiality of exchange doublets36. Under this condition, magnetic relaxation may proceed through multiple exchange doublets, rather than being limited by the energy of the first excited state, as in the case of an excited doublet with mixed exchange and crystal field character.
Modeling dc magnetic susceptibility data
A model of the electronic structure of these complexes using the following Hamiltonian reveals a more explicit correlation between lanthanide–radical coupling strength and the thermal barriers to magnetic relaxation37.
This model assumes a large axial anisotropy, represented by the parameter, as well as an isotropic exchange interaction between the angular momenta of the LnIII centers and the N23− radical spin38, 39. The χMT vs. T data may be reasonably modeled using lanthanide–radical exchange coupling values of JLn–rad = –7.2 and –23.1 cm−1 for 2-Dy and 2-Tb, respectively, along with slight modulation of g values around the expected g J values for DyIII and TbIII ions (further details are provided in Supplementary Methods, Supplementary Figs. 58 and 59, and Supplementary Tables 5 and 6). Excited state energies defined by Ising exchange coupling correspond to multiples of JLn–rad based on the magnitude of ΔJ resulting from a spin flip. For instance, in 2-Tb, the first excited state, corresponding to a flip of a single TbIII spin, has an energy of 12JTb–rad, while the second state, corresponding to a flip of the N23- radical spin, has an energy of 24JTb–rad. Using this formalism, Ueff estimates of 108 and 277 cm−1 can be obtained for 2-Dy and 2-Tb, respectively, in excellent agreement with the experimentally observed values of 108 and 276 cm−1. This model also estimates a second excited state energy double that of the first, or 554 cm−1 for 2-Tb, which is in reasonable agreement with the experimentally observed value of Ueff,2 = 564 cm−1.
The excited states defined by exchange coupling within these molecules will certainly mix with crystal field-split MJ states to generate a perturbed excited state spectrum, and a more accurate assessment of the electronic structure would therefore entail utilizing multiple exchange parameters36, 40. However, this simple model seems to have surprising utility for predicting excited state energies, and thereby magnetic relaxation barriers for lanthanide–radical molecules. In particular, it provides insight into the much lower Ueff values observed for 1-Dy and 2-Dy compared to 1-Tb and 2-Tb, which can be attributed to the substantially weaker exchange coupling in the dysprosium complexes. This model further provides a rationale for the very similar relaxation barriers for each pair of compounds, 1-Ln and 2-Ln: upon dissociation of THF, the geometry of the Ln2(μ−) core unit is scarcely perturbed, leading to similar exchange constants and comparable Ueff values.
Analysis of magnetic hysteresis and coercivity
Finally, single-molecule magnet performance in storage applications mandates retention of a non-zero magnetization under zero-applied field. Variable-field magnetization measurements were therefore performed using an average sweep rate of 0.01 T/s (Fig. 5). While 1-Dy does not display a remanent magnetization at any temperature, hysteresis loops for 2-Dy remain open up to 8 K, with a maximum Hc of 1 T at 5.5 K. The stark difference in hysteresis behavior between 1-Dy and 2-Dy again emphasizes the importance of THF removal from the metal centers as a means of enhancing axiality. Complex 1-Tb exhibits open hysteresis curves up to 15 K, with a maximum Hc of 3.7 T obtained at 11 K. In contrast, open magnetic hysteresis loops were observed for 2-Tb at temperatures as high as 30 K, and with a substantial Hc value of 0.48 T at 20 K. The coercive field steadily increases as the temperature is lowered to a giant coercive field of 7.9 T at 10 K, which then remains constant down to 2 K (Supplementary Figs. 60–61). Significantly, this is the largest coercive field yet observed for any molecule or coordination solid, and indeed is substantially larger than those of commercial permanent magnets, including Nd14Fe80B6 (iHc = 1.39 T at 298 K and 3.90 T at 77 K) and SmCo5 (iHc = 2.9 T at 298 K and iHc = 4.3 T at 4.2 K)41,42,43,44,45.
Modulation of the ligand field of the lanthanide ions in N23‒-radical-bridged dilanthanide complexes has produced valuable insights into the magnetic relaxation behavior for this important set of single-molecule magnets. As isolated in 1-Gd, 1-Tb, and 1-Dy, complexes of the type [(CpMe4H2Ln(THF))2(μ−)]− exhibit magnetic properties that are remarkably similar to those of the previously reported [(((Me3Si)2N)2Ln(THF))2(μ−)]− complexes, with replacement of the (Me3Si)2N− ligands with CpMe4H− ligands leading to comparable exchange coupling constants, relaxation barriers, blocking temperatures, and coercive fields (Table 1). Importantly, however, upon removal of the THF ligands to form [(CpMe4H2Ln)2(μ−)]– species, as isolated in 2-Tb and 2-Dy, a marked increase in magnetic anisotropy arises, leading to substantial increases in blocking temperatures and coercive fields. Indeed, 2-Tb displays a relaxation barrier of Ueff = 276 cm−1 and a 100-s blocking temperature of Tb = 20 K, both records for exchange-coupled single-molecule magnets, as well as a coercive field of Hc = 7.9 T at 10 K, the largest yet observed for any coordination compound. Furthermore, a simple model of the electronic structure for such radical-bridged dilanthanide complexes clearly relates the relaxation barrier to the exchange coupling constant, for example, through the equations Ueff = 12JTb-rad for diterbium(III) complexes and Ueff = 15JDy-rad for didysprosium(III) complexes. Thus, a path toward improved single-molecule magnets of this type is clear: replacing N23‒ with a radical bridge that provides stronger exchange coupling can be expected to increase Ueff substantially, while further adjustments to the ligand field arising from the capping ligands can enhance axiality, ensuring that the observed blocking temperature is not diminished by through-barrier relaxation processes and potentially yielding even greater coercive fields.
The manipulations described below were performed under an inert atmosphere with rigorous exclusion of air and water using Schlenk, vacuum line, and glovebox techniques. Solvents were dried using a commercial solvent purification system from JC Meyer Solvent Systems (http://www.jcmeyer-solventsystems.com). The precursor 1,2,3,4-tetramethylcyclopentadiene (CpMe4HH) was purchased from Sigma-Aldrich and dried over 4 Å sieves before use. Anhydrous LnCl3 (Ln = Gd, Tb, Dy) was purchased from Sigma-Aldrich and used as received. Potassium bis(trimethylsilyl)amide, KN[Si(CH3)3]2, was purchased from Sigma-Aldrich, dissolved in toluene, filtered through Celite, and recrystallized from toluene at −35 °C before use. The compound 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]-hexacosane (2.2.2-cryptand; here abbreviated as crypt-222) was purchased from TCI America and used as received. The compounds, KCpMe4H29 and KC846, were prepared according to literature procedures. Synthesis details for the precursor complexes CpMe4H2Ln(η3-C3H5) and CpMe4H2Ln(BPh4), (Supplementary Figs. 62–67), where Ln = Gd, Tb, Dy, are described in the Supplementary Methods, and their preparation followed closely the route used for CpMe4H2Lu(BPh4) or CpMe4H2Sc(BPh4)29, 30. Preparation of the complexes CpMe4H2Ln(µ-Cl2)K(THF) x and (CpMe4H2Ln(THF))(µ-N2), 3-Ln, (Supplementary Figs. 68–80), generally followed routes previously described in the literature for LuIII and ScIII analogs29, 30, while syntheses and modifications made in the case of 3-Ln are described below. The structures of (CpMe4H2Ln(THF))2(µ−N2), where Ln = Gd, Dy were published previously, although (CpMe4H2Dy(THF))2(µ−N2) was reported in a different cell, and these compounds were synthesized by reduction of (C5Me4H)3Ln(THF)47. Elemental analyses were performed by the Micro-Mass Facility at the University of California, Berkeley, using a Perkin-Elmer Series 2400 Series II combustion analyzer. IR spectra were recorded on a Perkin-Elmer Avatar Spectrum 400 FTIR Spectrometer equipped with ATR.
General procedure for the synthesis of (CpMe4H 2Ln(THF))2(µ−N2 .), 3-Ln, Ln = Gd, Tb, Dy
In a nitrogen-filled glovebox, CpMe4H2Ln(BPh4) was dissolved in 15 ml of THF to give a colorless solution. Subsequently, potassium graphite was added at once whereby the solution color turned to orange–red. After 5 min of stirring at room temperature, black and white insoluble materials, presumably graphite and KBPh4, were removed by filtration. The orange–red filtrate was pumped down under reduced pressure to yield a solid that was extracted with 5 ml of toluene to afford a dark red solution. Green crystals of (CpMe4H2Ln(THF))2(µ−N2) suitable for X-ray analysis were grown in the freezer over the course of 48 h.
3-Gd: Isolated 263 mg in crystalline yield (49%) from the reaction of 790 mg (1.10 mmol) of crystalline CpMe4H2Gd(BPh4) and 149 mg (1.10 mmol) of potassium graphite. IR (neat): 2962 m, 2905 s, 2855 s, 2716 w, 1443 m, 1377 w, 1327 w, 1242 w, 1173 w, 1108 w, 1030 s, 917 w, 890 m, 875 s, 833 w, 777 s, 762 s, 741 m, 613 s cm−1Anal. Calcd for C44H68N2O2Gd2: C, 54.40; H, 7.06; N, 2.88. Found: C, 54.76; H, 7.21; N, 2.77.
3-Tb: Isolated 162.9 mg in crystalline yield (52%) from the reaction of 460.4 mg (0.639 mmol) of crystalline CpMe4H2Tb(BPh4) and 86.4 mg (0.639 mmol) of potassium graphite. IR (neat): 2960 m, 2930 m, 2905 s, 2895 s, 2858 s, 1459 m, 1446 m, 1437 m, 1429 m, 1376 m, 1368 m, 1030 s, 917 m, 874 s, 860 s, 780 s, 765 s, 743 s, 663 m, 655 m, 615 s, 600 s cm−1. Anal. Calcd for C44H68N2O2Tb2: C, 54.21; H, 7.03; N, 2.87. Found: C, 54.31; H, 7.03; N, 2.79.
3-Dy: Isolated 131.2 mg in crystalline yield (55%) from the reaction of 350.3 mg (0.4837 mmol) of crystalline CpMe4H2Tb(BPh4) and 65.4 mg (0.484 mmol) of potassium graphite. IR (neat): 2954 m, 2936 m, 2901 s, 2857 s, 2858 s, 1461 m, 1448 m, 1441 m, 1432 m, 1426 m, 1379 m, 1370 m, 1202 w, 1030 s, 916 w, 874 s, 862 s, 781 s, 763 s, 742 m, 665 m, 626 m, 616 s, 611 s cm−1. Anal. Calcd for C44H68N2O2Dy2: C, 53.81; H, 6.98; N, 2.85. Found: C, 53.84; H, 7.10; N, 2.82.
General procedure for the synthesis of [K(crypt-222)(THF)][(CpMe4H 2Ln(THF))2(µ−N2 .)], 1-Ln, Ln = Gd, Tb, Dy
In an argon-filled glovebox, a 10 ml THF solution containing crypt-222 (6 ml in the case of Dy) was added to a 10 ml pale green THF solution of crystalline (CpMe4H2Ln(THF))2(µ−N2) (6 ml in the case of Dy). Subsequently, potassium graphite was added at once to the reaction mixture, whereby the solution color turned to red–brown. After 5 min of stirring at room temperature, black insoluble material, presumably graphite, was removed by filtration. The dark brown filtrate was stored in the freezer for 24 h to afford dark brown crystals of 1-Ln that were suitable for X-ray analysis.
1-Gd: Isolated 128 mg in crystalline yield (75%) from the reaction of 113.9 mg (0.1166 mmol) of crystalline (CpMe4H2Gd(THF))2(µ−N2), 43.9 mg (0.117 mmol) of crypt-222, and 15.8 mg (0.117 mmol) potassium graphite. IR (neat): 2939 m, 2881 s, 2844 s, 2711 w, 1473 w, 1458 w, 1444 w, 1353 s, 1329 w, 1314 w, 1297 w, 1283 w, 1261 w, 1244 w, 1172 w, 1132 m, 1102 s, 1076 m, 1062 s, 1042 m, 1029 m, 946 s, 922 m, 901 m, 862 w, 826 w, 809 w, 788 w, 763 m, 746 m, 727 m, 727 w, 716 w, 702 w, 663 w, 616 w, 600 w cm−1. Anal. Calcd for C66H112KN4O9Gd2: C, 54.32; H, 7.74; N, 3.84. Found: C, 54.50; H, 7.89; N, 3.78.
1-Tb: Isolated 168 mg in crystalline yield (78%) from the reaction of 144 mg (0.148 mmol) of crystalline (CpMe4H2Tb(THF))2(µ−N2), 55.7 mg (0.148 mmol) of crypt-222, and 20.0 mg (0.148 mmol) of potassium graphite. IR (neat): 2940 mbr, 2879 s, 2846 s, 2712 w, 1474 w, 1455 m, 1443 m, 1352 s, 1297 w, 1283 w, 1260 w, 1243 w, 1171 w, 1132 s, 1102 s, 1077 s, 1062 s, 1044 s, 1030 s, 947 s, 931 m, 922 m, 903 m, 856 w, 831 w, 824 w, 765 m, 746 s, 727 w, 615 w, 557 s cm−1. Anal. Calcd for C66H112KN4O9Tb2: C, 54.20; H, 7.72; N, 3.83. Found: C, 54.13; H, 7.85; N, 3.80.
1-Dy: Isolated 63.8 mg in crystalline yield (57%) from the reaction of 74.5 mg (0.0759 mmol) of crystalline (CpMe4H2Dy(THF))2(µ−N2), 28.6 mg (0.0759 mmol) of crypt-222, and 10.3 mg (0.0759 mmol) of potassium graphite. IR (neat): 2938 mbr, 2878 s, 2847 s, 1476 m, 1459 m, 1452 m, 1443 m, 1353 s, 1298 w, 1284 w, 1259 w, 1242 w, 1172 w, 1133 s, 1101 vs, 1062 s, 1043 s, 947 s, 931 m, 922 m, 903 m, 883 w, 853 w, 822 w, 767 m, 746 s, 696 w, 672 w, 641 w, 614 w, 560 s cm−1. Anal. Calcd for C66H112KN4O9Dy2: C, 53.94; H, 7.68; N, 3.81. Found: C, 53.85; H, 7.88; N, 4.00.
Procedure for the synthesis of [K(crypt-222)][(CpMe4H 2Ln)2(µ−N2 .)], 2-Ln, Ln = Tb, Dy
2-Tb: In an argon-filled glovebox, [K(crypt-222)(THF)][(CpMe4H2Tb(THF))2(µ−N2)] (92.0 mg, 0.063 mmol) was dissolved in 12 ml of 2-MeTHF to give a brown–black solution. The solution was filtered and the brown–black filtrate was stored in the freezer for 48 h to afford brown–black crystals of 2-Tb that were suitable for X-ray analysis (76 mg, 91%). Anal. Calcd for C59H98KN4O7Tb2: C, 53.19; H, 7.41; N, 4.21. Found: C, 53.34; H, 7.46; N, 4.12.
2-Dy: The same procedure was used as above, with 62.0 mg (0.042 mmol) [K(crypt-222)(THF)][(CpMe4H2Dy(THF))2(µ−N2)], and 10 ml of 2-MeTHF to give a brown–black solution, which was filtered and stored in the freezer for 48 h to afford brown–black crystals of 2-Dy that were suitable for X-ray analysis (51.0 mg, 90%). IR (neat): 2956 m, 2878 s, 2852 s, 2717 w, 1477 m, 1456 m, 1442 m, 1378 w, 1354 s, 1296 m, 1259 m, 1132 s, 1101 vs, 1079 s, 1022 m, 947 s, 932 s, 828 m, 819 m, 803 w, 765 s, 749 s, 620 m, 567 vs cm−1. Anal. Calcd for C59H98KN4O7Dy2: C, 52.90; H, 7.37; N, 4.18. Found: C, 53.06; H, 7.23; N, 4.28.
Synthesis of [K(crypt-222)][(CpMe4H 2Gd(2-MeTHF)2(µ−N2 .)], 4
In an argon-filled glovebox, [K(crypt-222)(THF)][(CpMe4H2Gd(THF))2(µ−N2.)] (96.0 mg, 0.066 mmol) was dissolved in 10 ml of 2-MeTHF to give a brown–black solution. The solution was filtered and the brown–black filtrate was stored in the freezer for 48 h to afford brown–black crystals of 4 that were suitable for X-ray analysis (86.0 mg, 92%). IR (neat): 2952 m, 2879 s, 2842 s, 2711 w, 1473 m, 1441 m, 1376 w, 1350 m, 1327 w, 1297 m, 1256 m, 1232 w, 1172 w, 1131 s, 1114 s, 1101 vs, 1076 s, 1057 s, 1031 m, 1015 m, 991 w, 966 w, 951 s, 932 s, 896 w, 869 w, 859 w, 833 w, 820 m, 798 w, 751 s, 700 w, 684 w, 654 w, 615 w cm−1. Anal. Calcd for C64H108KN4O8Gd2: C, 54.32; H, 7.69; N, 3.96. Found: C, 54.10; H, 7.80; N, 3.82.
Structural characterization of compounds
X-ray diffraction experiments were performed at 100 K on crystals coated with paratone-N oil and mounted on Kapton or MiTeGen loops. Data were collected at the small molecule X-ray crystallography facility at the University of California, Berkeley using a Bruker QUAZAR diffractometer equipped with a microfocus sealed X-ray source (Mo-Kα radiation; λ = 0.71073 Å) and a Bruker APEX-II detector for 2-Tb, 4, 3-Dy, CpMe4H2Dy(BPh4), CpMe4H2Gd(BPh4), CpMe4H2Tb(allyl), and CpMe4H2Dy(allyl), or at Beamline 11.3.1 at the Advanced Light Source on a Bruker D8 Diffractometer equipped with a Bruker PHOTON100 CMOS detector using synchrotron radiation with λ = 0.6888 Å for 1-Dy and CpMe4H2Gd(allyl) and λ = 0.7749 Å for 1-Gd, 1-Tb, 2-Dy, 3-Tb, 3-Gd, and CpMe4H2Tb(BPh4) (further details are provided in Supplementary Methods and Supplementary Tables 7–9). Crystallographic data have been deposited in the Cambridge Structural Database as CCDC 1547761 (2-Tb),1547762 (2-Dy),1547763 (4), 1547764 (1-Tb) 1547765 (1-Dy), 1547766 (1-Gd), 1547767 (3-Tb), 1547768 (3-Dy), 1547769 (3-Gd), 1547770 (CpMe4H2Tb(BPh4)), 1547771 (CpMe4H2Dy(BPh4)), 1547772 (CpMe4H2Gd(BPh4)), 1547773 (CpMe4H2Tb(allyl)), 1547774 (CpMe4H2Dy(allyl)), 1547775 (CpMe4H2Gd(allyl)).
Magnetic susceptibility measurements
The magnetic samples of 1-Ln (Ln = Gd, Tb, Dy), 2-Ln (Ln = Tb, Dy), and 3-Ln (Ln = Gd, Dy, Tb) were prepared by adding crushed crystalline samples to 7 mm quartz tubes. Sufficient liquid eicosane (at 40 °C) was added to saturate and cover the samples to prevent crystallite torqueing and provide good thermal contact between the sample and the bath. Tubes were fitted with sealable adapters, evacuated on a Schlenk line, and flame sealed under vacuum using a H2/O2 flame. Magnetic susceptibility measurements were collected using a Quantum Design MPMSXL SQUID magnetometer. For the hysteresis loops of 2-Tb, magnetic susceptibility measurements were collected using a Quantum Design 14 Tesla Dynacool magnetometer at the facility of Quantum Design in San Diego, CA. High-frequency ac measurements were also performed at the facility of Quantum Design in San Diego, CA, where a 9 T PPMS equipped with the ACMSII measurement option to probe the ac relaxation at frequencies above 1500 Hz was used. Dc susceptibility data measurements were performed at temperatures ranging from 2 to 300 K for 1-Ln (Ln = Gd, Tb, Dy), 2-Ln (Ln = Tb, Dy), and 3-Ln (Ln = Gd, Dy, Tb) using applied fields of 1000, 5000, and 10,000 Oe. Ac magnetic susceptibility data measurements were performed using a 4 Oe switching field. All data were corrected for diamagnetic contributions from the eicosane and core diamagnetism estimated using Pascal’s constants48. Cole-Cole plots were fitted using formulae describing χ′ and χ″ in terms of frequency, constant temperature susceptibility (χT), adiabatic susceptibility (χS), relaxation time (τ), and a variable representing the distribution of relaxation times (α)33. All data were fitted to α values of ≤0.09.
Details for modeling dc magnetic susceptibility data
Magnetic susceptibility data for 1-Dy, 1-Tb, 2-Dy, and 2-Tb were modeled using the Hamiltonian given in Eq. (1) above, where JLn-rad corresponds to the magnetic exchange between the radical spin and the J multiplets of the lanthanide ions49. The operator assigns a uniaxial anisotropy parameter to the lanthanide J multiplets. When a strongly axial doublet ground state of DyIII or TbIII is obtained, its magnetic exchange with an isotropic spin can be assumed to be Ising in nature50. The excited state spectrum for a molecule with dominant Ising exchange should correspond to the energies required for different spin flips, , where ΔE reflects both the exchange coupling strength and the change in total angular momentum between the ground state and the spin-flip-generated excited state. Using the values of JLn–rad determined using the Hamiltonian given in Eq. (1), spin-flip energies, ΔE, were estimated for comparison with the experimental barriers, Ueff.
Crystallographic data have been deposited in the Cambridge Structural Database as specified above for each compound under the deposition numbers CCDC 1547761-1547775 that is available free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. All other data can be obtained from the authors on request.
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This research was supported by National Science Foundation (NSF) Awards CHE-1464841 to J.R.L. and CHE-1565776 to W.J.E. We thank the NSF Graduate Research Fellowship Program for support of L.E.D. X-ray diffraction data were collected at Beamline 11.3.1 at the Advanced Light Source and the UC Berkeley Small Molecule X-ray Crystallography Facility (Chexray). The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences, of the U.S. DOE under Contract No. DE-AC02-05CH11231. The ChexQuazar instrument employed at the UC Berkeley Chexray facility is supported by an NIH Shared Instrumentation Grant S10‐RR027172. We thank Dr Shi Li, Dr Neil Dilley, and Dr Randy Dumas for assistance at the facilities of Quantum Design in San Diego, and Dr Wayne Lukens, Dr Joseph Zadrozny, Dr Krunoslav Prsa, and Prof. Oliver Waldmann for helpful discussions.
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