Abstract
The reaction of a saddle-distorted Mo(v)-dodecaphenylporphyrin complex and a Keggin-type polyoxometalate gives a discrete and nanosized molecule, [{Mo(DPP)(O)}2(H2SiW12O40)], which involves direct coordination between the Mo(v) centers and terminal oxo groups of the polyoxometalate and exhibits excellent stability in solution to show reversible multi-redox processes.
Original language | English |
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Pages (from-to) | 3997-3999 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 39 |
DOIs | |
State | Published - 2007 |