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Mono‐ and bis‐salen functionalised [2]rotaxanes have been synthesised from the esterification of [2]rotaxanes containing phenol‐terminated threads (salen=N,N′‐bis(salicylidene)ethylenediamine). The [2]rotaxanes have general formula [RH][Cr7NiF8(O2CtBu)16], where [RH]+ is a thread with a central secondary ammonium site that templates a [Cr7NiF8(O2CtBu)16]− ring. The threads are terminated at one or both ends by carboxylic acid functionalised salen groups. The {M(salen)} groups can be free‐base [M=(H+)2] or metallated [M=Cu2+, Ni2+, (VO)2+]. The [2]rotaxanes have been characterised by single crystal XRD and solid‐ and solution‐state EPR spectroscopy. Where two paramagnetic M ions are involved [M=Cu2+ and/or (VO)2+] the [2]rotaxanes contain three electron spin S=1/2 ${{ 1/2 }}$ centres, since the {Cr7Ni} ring has an S=1/2 ${{ 1/2 }}$ ground state which is well isolated at low temperatures. These three‐spin [2]rotaxanes have been characterised in solution by pulsed dipolar EPR spectroscopies (DEER, also known as PELDOR, and RIDME). The M⋅⋅⋅M and M⋅⋅⋅{Cr7Ni} interactions measured are consistent with dipolar interactions and also with the distances from single crystal XRD. The authors declare no competing financial interest. [ABSTRACT FROM AUTHOR]

We report the synthesis of a series of temperature‐sensitive non‐classical early Ln(II) (Ln=lanthanide) complexes, [K(2.2.2‐cryptand)][Ln(Cptt)3] (Cptt=C5H3tBu2‐1,3; 1‐Ln; Ln=La−Nd). Complexes 1‐Ln were typically prepared using Schlenk line techniques rather than more common glove box protocols, by the reduction of the parent Ln(III) complexes [Ln(Cptt)3] (2‐Ln) with KC8 in THF in the presence of 2.2.2‐cryptand at −30 °C. The majority of the 2‐Ln series have been reported previously by the salt metathesis reactions of 3 eq. KCptt with parent LnCl3, and these methods were adapted here to afford 2‐Pr. Complexes 1‐Ln and 2‐Pr were characterized by single crystal XRD, elemental analysis, ATR‐IR and UV‐Vis‐NIR spectroscopy; 1‐La and 2‐Pr were additionally characterized by c.w. EPR spectroscopy, and variable temperature magnetic susceptibility measurements were performed on 2‐Pr. During attempts to synthesize 2‐Nd and 2‐Sm we also obtained small crops of crystals of [Nd(Cptt)2(μ‐I)]2 (3) and [Sm(Cptt)2(μ‐Cl)]2 ⋅ C7H8 (4 ⋅ C7H8), respectively; these complexes were also structurally authenticated, and magnetic data was collected for 4 ⋅ C7H8. The combination of data obtained indicate that the Ln(II) centers in 1‐Ln adopt 4fn5d1 electron configurations, in common with other literature examples of [Ln(CpR)3]− anions (CpR=substituted cyclopentadienyl) for these metals. [ABSTRACT FROM AUTHOR]

We report the synthesis and structural characterization of a series of heterometallic rings templated via alkylammonium or imidazolium cations. The template and preference of each metal's coordination geometry can control the structure of heterometallic compounds, leading to octa-, nona-, deca-, dodeca-, and tetradeca-metallic rings. The compounds were characterized by single-crystal X-ray diffraction, elemental analysis, magnetometry, and EPR measurements. Magnetic measurements show that the exchange coupling between metal centres is antiferromagnetic. EPR spectroscopy shows that the spectra of {Cr7Zn} and {Cr9Zn} have S = 3/2 ground states, while the spectra of {Cr12Zn2} and {Cr8Zn} are consistent with S = 1 and 2 excited states. The EPR spectra of {(ImidH)-Cr6Zn2}, {(1-MeImH)-Cr8Zn2}, and {(1,2-diMeImH)-Cr8Zn2} include a combination of linkage isomers. The results on these related compounds allow us to examine the transferability of magnetic parameters between compounds. [ABSTRACT FROM AUTHOR]

Polymer beads have been used as the core of magnetic particles for around twenty years. Here we report studies to attach polymetallic complexes to polymer beads for the first time, producing beads of around 115 microns diameter that are attached to 1014 hybrid inorganic-organic [2]rotaxanes. The bead is then formally a [1014] rotaxane. The number of complexes attached is counted by EPR spectroscopy after including TEMPO radicals within the thread of the hybrid [2]rotaxanes. Polymer beads are used in the core of magnetic particles, and beads functionalised with paramagnetic molecules are promising as agents for dynamic nuclear polarization. Here, the authors use conventional click chemistry to decorate a polymer bead with 1014 [2]rotaxanes containing paramagnetic {Cr7Ni} rings. [ABSTRACT FROM AUTHOR]

Compounds of general formula [Cr7MF3(Etglu) - (O2CtBu)15Phpy)] [H5Etglu = N-ethyl-D-glucamine; Phpy = 4-phenylpyridine; M = Zn (l), Mn (2), Ni (3)] have been prepared. The structures contain an irregular octagon of metal sites formed around the pentadeprotonated Etglu5- ligand; the chirality of N-ethyl-D-glucamine is retained in the final product. The seven CrIII sites have a range of coordination environments, and the divalent metal site is crystallographically identified and has a Phpy ligand attached to it. By using complementary experimental techniques, including magnetization and specific heat measurements, inelastic neutron scattering, and electron paramagnetic resonance spectroscopy, we have investigated the magnetic features of this family of {Cr7M} rings. Microscopic parameters of the spin Hamiltonian have been determined as a result of best fits of the different experimental data, allowing a direct comparison with corresponding parameters found in the parent compounds. We examine whether these parameters can be transferred between compounds and compare them with those of an earlier family of heterometallic rings. [ABSTRACT FROM AUTHOR]