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Volumn 34, Issue 22, 1995, Pages 2535-2537

A Dinuclear (μ‐Carboxylato)manganese(II) Complex Derived from a Macrocyclic Ligand: A Structural Model for Active Sites in Natural Systems

Author keywords

complexes with nitrogen ligands; D xylose isomerase; enzymes; manganese compounds

Indexed keywords

EID: 33748227279 PISSN: 05700833 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.199525351 Document Type: Article

Times cited : (29)

References (29)

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- +. No peaks are observed that can be assigned to a species retaining the intact Schiff base cryptand.

18
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- 2 was used in the latter stages of refinement. Complex scattering factors were taken from the program package SHELXTL/PC [15] as implemented on the Viglen 486dx computer. Further details of the crystal structure investigation may be obtained from the Director of the Cambridge Crystallographic Data Centre, 12 Union Road, GB‐Cambridge, CB2 1EZ (UK), on quoting the full journal citation.

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27
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- Multifield saturation magnetization data were collected on crystals of the complex using a Quantum Design MPMS squid magnetometer. Measurements were performed in the 5–300 K temperature range at six field strengths (0.5, 1, 2, 3, 4, 5 Tesla). The magnetization of the sample holder (kel F bucket) was measured at the same temperatures and field strengths and subtracted from the sample measurements. The diamagnetic correction was estimated from Pascals constants.

28
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- iz is defined in Equation (b). J is the isotropic exchange interaction and D and E are the axial and rhombic parameters of the zero‐field splitting tensors. In agreement with the structural data, the two metal sites are assumed to be identical. The usual hypothesis is made that for each ion the zero‐field splitting and g tensors can be diagonalized simultaneously.

29
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- EPR spectra were measured in the range 4–20 K on a Varia E9 spectrometer operating at 9.2 GHz equipped with an Oxford cryostat.

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