Abstract
The reaction of Mn(OAc)2·4H2O with 2,6-dimethoxybenzoylsalicylhydrazide (H3dmbshz) leads to a dodecanuclear manganese metallamacrocycle [Mn12(dmbshz) 12(EtOH)6], 1. The successive manganese centers are connected by the hydrazide N-N groups of the ligands in an alternating pentadentate binding mode, hexadentate binding mode. The alternation results in two alternating chelation modes around the metal centers, a tridentate- tridentate chelation mode and a bidentate-tridentate chelation mode. The metal ions in 1 are in a ⋯(AAΔBC AΛB)(AAΔBC AΛB)⋯ chiral sequence, the alternation of the chiralities expanding the cyclic ring system to a 36-membered dodecanuclear manganese metallamacrocyclic ring system with S6 point group symmetry.
Original language | English |
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Pages (from-to) | 6579-6583 |
Number of pages | 5 |
Journal | Dalton Transactions |
Issue number | 46 |
DOIs | |
State | Published - 2008 |