Journal
INORGANIC CHEMISTRY
Volume 53, Issue 5, Pages 2692-2698Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ic403098p
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Funding
- National Science Foundation (NSF) [CHE-1263760, DBIO 722538]
- NSF-Graduate Research Fellowship Program [DGE-1148897]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1263760] Funding Source: National Science Foundation
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Treatment of the cobalt(II) amide, [Co{N(SiMe3)(2)}(2)](2), with four equivalents of the sterically crowded terphenyl phenols, HOArMe6 (Ar-Me6 = C6H3-2,6(C6H2-2,4,6-Me-3)(2)) or HOAriPr4 (Ar-iPr4 = C6H3-2,6(C6H3-2,6-Pr-2(i))(2)), produced the first well-characterized, monomeric two-coordinate cobalt(II) bisaryloxides, Co(OArMe6)(2) (1) and Co(OAriPr4)2 (2a and 2b), as red solids in good yields with elimination of HN(SiMe3)(2). The compounds were characterized by electronic spectroscopy, X-ray crystallography, and direct current magnetization measurements. The O-Co-O interligand angles in 2a and 2b are 180 degrees, whereas the O-Co-O angle in 1 is bent at 130.12(8)degrees and its cobalt(II) ion has a highly distorted pseudotetrahedral geometry with close interactions to the ipso-carbons of the two flanking aryl rings. The Co-O distances in 1, 2a, and 2b are 1.858(2), 1.841(1), and 1.836(2) angstrom respectively. Structural refinement revealed that 1, 2a, and 2b have different fractional occupations of the cobalt site in their crystal structures: 1, 95.0%, 2a, 93.5%, and 2b, 84.6%. Correction of the magnetic data for the different cobalt(II) occupancies showed that the magnetization of 2a and 2b was virtually identical. The effective magnetic moments for 1, 2a, and 2b, 5.646(5), 5.754(5), and 5.636(3) mu(B) respectively, were indicative of significant spin orbit coupling. The differences in magnetic properties between 1 and 2a/2b are attributed to their different cobalt coordination geometries.
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