Ensheathing a polyoxometalate: Convenient systematic introduction of organoimido ligands at terminal oxo sites in [Mo[sub 6]O[sub 19]][sup 2[minus]]
- Kansas State Univ., Manhattan, KS (United States)
- Univ. of Delaware, Newark, DE (United States)
We report a simple and general method for the direct functionalization of the hexamolybdate cluster, [Mo[sub 6]O[sub 19]][sup 2[minus]], through which peripheral oxo ligands can be systematically replaced by a variety of organoimido groups. In the case of the 2,6-(diisopropylphenyl)imido ligand (hereafter referred to as NAr), we have discovered that multiple functionalization is readily achieved. The availability of these homologous oxo/(NAr) hexamolybdate derivatives provides an opportunity to examine how the electrochemical properties of the clusters respond to varying degrees of substitution. Cyclic voltametry studies in acetonitrile were conducted on the hexamolybdate and its mono-, bis-, and tetrakis(NAr) derivatives. Given the ready availability of various organic isocyanates, the present work suggests that it will be possible to logically design and rationally synthesize a broad range of hexamolybdate derivatives of potential utility. 11 refs., 3 figs.
- DOE Contract Number:
- FG02-92ER14246
- OSTI ID:
- 7069653
- Journal Information:
- Journal of the American Chemical Society; (United States), Vol. 116:8; ISSN 0002-7863
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
MOLYBDENUM COMPOUNDS
DERIVATIZATION
VOLTAMETRY
ACETONITRILE
ELECTROCHEMISTRY
LIGANDS
CHEMICAL REACTIONS
CHEMISTRY
NITRILES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
REFRACTORY METAL COMPOUNDS
TRANSITION ELEMENT COMPOUNDS
400201* - Chemical & Physicochemical Properties
400400 - Electrochemistry