New hexaaza macrocyclic binucleating ligands ... - ACS Publications

Mar 1, 1991 - Oxygen insertion with a dicopper(I) Schiff base macrocyclic complex [Erratum to document cited in CA113(24):223409t]. Rached. Menif, Art...
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1428 Inorganic Chemistry, Vol. 30, No. 6, 1991

Additions and Corrections

N . 0, CI) and 25b (Mo). the non-hydrogen atoms being corrected for anomalous dispersion.2sc Final atomic coordinates for the non-hydrogen atoms are given in Table 11. Selected bond distances and angles are given in Table I l l . The structural model adopted is for a site-disordered crystal of 1. CH2CI,. In this model the site labeled CI( 1 ) is occupied by a terminal chloro ligand :ind :I tcrminnl oxo ligand. cach with 0.5 occupancy. Refincmcnt in the noncentric space group Cc resulted in wide discrepancies bctwccn thc bond lengths and angles in the two halves of the molecule, (27) Johnson, C. K.

ORTEP 11. Report ORNL-5138: Oak Ridge National Laborntor): Oak Ridgc, T N , 1976.

and refinement of the dichloromethane molecule was unsatisfactory.

Acknowledgment. We t h a n k Dr. Keith S. M u r r a y a n d Ms. Karen Bertoncello for assistance with t h e susceptibility measurements and Dr. S. Middleton for t h e mass spectrum. We gratefully acknowledge the financial assistance of the Australian Research Council. Supplementary Material Available: Complete listings of crystal and experimental data, positional atomic data, thermal parameters, and bond distances and angles (7 pages); a listing of observed and calculated structure amplitudes (30 pages). Ordering information is given on any current masthead page,

Additions and Corrections 1990, Volume 29

Rached Menif, Arthur E. Martell,* Philip J. Squattrito, and Abraham Clearfield: New Hexaaza Macrocyclic Binucleating Ligands. Oxygen Insertion with a Dicopper(1) Schiff Base Macrocyclic Complex. Page 4725. Replace Figure 1 by the following figure. This is necessary in order that the atomic numbering scheme corresponds to the numbers in Tables 11-IV. a

-Arthur

E. Martell