Tunable single-molecule magnets: The spin-level landscape in a series of Fe(III) (4) single-molecule magnets with propeller-like structure was analyzed by means of high-frequency EPR spectroscopy. The zero-field splitting parameter D of the ground S=5 spin state correlates strongly with the pitch of the propeller gamma (see picture), and thus provides a simple link between molecular structure and magnetic behavior.We report three novel tetrairon(III) single-molecule magnets with formula [Fe(4)(L)(2)(dpm)(6)] (Hdpm=2,2,6,6-tetramethylheptane-3,5-dione), prepared by using pentaerythritol monoether ligands H(3)L=R'OCH(2)C(CH(2)OH)(3) with R'=allyl (1), (R,S)-2-methyl-1-butyl (2), and (S)-2-methyl-1-butyl (3), along with a new crystal phase of the complex containing H(3)L=11-(acetylthio)-2,2-bis(hydroxymethyl)- undecan-1-ol (4). High-frequency EPR (HF-EPR) spectra at low temperature were collected on powder samples in order to determine the zero-field splitting (zfs) parameters in the ground S=5 spin state. In 1-4 and in other eight isostructural compounds previously reported, a remarkable correlation is found between the axial zfs parameter D and the pitch gamma of the propeller-like structure. The relationship is directly demonstrated by 1, which features both structurally and magnetically inequivalent molecules in the crystal. The dynamics of magnetization has been investigated by ac susceptometry, and the results analyzed by master-matrix calculations. The large rhombicities of 2 and 3 were found to be responsible for the fast magnetic relaxation observed in the two compounds. However, complex 3 shows an additional faster relaxation mechanism which is unaccounted for by the set of spin Hamiltonian parameters determined by HF-EPR.

Abstract“Alligator clips” suitable for grafting on H‐terminated silicon or gold surfaces have been incorporated into single‐molecule magnets (SMMs) of the Fe4 family. Tripodal ligands 2,2‐bis(hydroxymethyl)‐10‐undecen‐1‐ol (H3L1) and 11‐(acetylthio)‐2,2‐bis(hydroxymethyl)undecan‐1‐ol (H3L2) have been used to replace the six methoxide bridges in [Fe4(OMe)6(dpm)6], affording new Fe4 derivatives [Fe4(L1)2(dpm)6] (1) and [Fe4(L2)2(dpm)6] (2) in high yield (Hdpm = dipivaloylmethane). The molecular structures have been unambiguously established by XRD combined with ESI‐MS and magnetic characterization techniques, including DC and AC magnetometry and high‐frequency EPR spectroscopy. The two SMMs have an S = 5 ground state and an easy‐axis magnetic anisotropy leading to slow relaxation of the magnetization at low temperature, with effective anisotropy barriers of 15.9(2) K in 1 and 15.1(2) K in 2. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

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Amberlite IRA900N3 is an excellent organocatalyst for the azidation of alpha,beta-unsaturated ketones with trimethylsilyl azide under solvent-free conditions. By avoiding the use of metallic species and of the organic reaction medium, the procedure is a green tool for the preparation of beta-azido ketones under mild conditions with yields from good to excellent. The catalyst can be recovered and re-used with no loss of its efficiency.

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[structure: see text]. The first examples of selectively functionalized calix[7]arenes have been obtained by weak-base promoted O-alkylation or O-benzoylation of p-tert-butylcalix[7]arene. Mono-, 1,3- and 1,4-disubstituted calix[7]arenes have been obtained in workable yields, while the 1,2,4,6-tetrasubstitution was achieved with surprisingly high selectivity (50-88% yield) by using K2CO3 as base. A rationale for this finding is proposed.