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- W2009708963 abstract "Cyclic-voltammetric studies in CH2Cl2 have shown that [Mn(η-C5H5–nMen)(CO)3–xLx][n= 0, 1, or 5, x= 1, L = phosphine or phosphite (1); n= 0 or 1, x= 2, L =½dppe (dppe = Ph2PCH2CH2PPh2), PPh3, or PMePh2] each undergo a reversible one-electron oxidation to [Mn(η-C5H5–nMen)(CO)3–xLx]+[x= 1 (3) or 2 (4)]. The paramagnetic cations (3) may be generated chemically by silver(I) ion oxidation of (1), and (4) may be isolated from either silver(I) ion or diazonium ion oxidation of (2). On reaction with [N(C6H4Br-p)3][SbCl4], SbCl5, Br2, or I2, (1) and (2) afford the diamagnetic complexes [MnX(η-C5H5–nMen)(CO)3–xLx]+[X = Cl, Br, or I, x= 1 (5) or 2 (6)], via the attack of halogen radicals on (3) or (4). The relation between the oxidation potential, Ep, and k(CO), the force constant for the carbonyl-stretching vibrations, for (1), (2), and [Mn(η-C5H5–nMen)(CO)3] is discussed with reference to that previously reported for the isoelectronic chromium complexes [Cr(η-C6Me6)(CO)2L]." @default.
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- W2009708963 title "Reduction–oxidation properties of organotransition-metal complexes. Part 5. The one-electron oxidation of tricarbonyl(η-cyclopentadienyl)-manganese derivatives and the reactivity of the resulting radical cations" @default.
- W2009708963 doi "https://doi.org/10.1039/dt9770000931" @default.
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