期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 128, 期 10, 页码 3281-3290出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja0582962
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Unprecedented strong electronic communication has been found in dimolybdenum pairs containing quadruply bonded Mo-2(DAniF)(3)(+) (DAniF = N,N'-di-p-anisylformamidinate) units linked by dioxolene (C6X2O42-) anions. The neutral compounds [Mo-2(DAniF)(3)](2)(C6X2O4) (1, X = H; 2, X = Cl; 3, X = NO2) and the singly oxidized products {[Mo-2(DAniF)(3)](2)(C6X2O4)Mo-2}PF6 (4, X = H; 5, X = Cl) have been synthesized and characterized by X-ray crystallography and spectroscopic methods. Unusually short Mo-O distances (similar to 2.05 angstrom for 1 and 2, and similar to 2.01 angstrom for 4 and 5) are implicated in the remarkably strong interaction between [Mo-2] units via the linkers. This leads to an extensive charge delocalization in the mixed-valence species, which is mediated by the dioxolene linker, as revealed by the large Delta E-1/2 values (763, 795, and 816 mV for 1, 2, and 3, respectively). Additional evidence for the strong electronic coupling is provided by UV-vis, NIR, and EPR spectroscopies and DFT calculations.
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