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Variable Nitric Oxide Reactivity of Tropocoronand Cobalt(III) Nitrite Complexes as a Function of the Polymethylene Linker Chain Length

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NIAID Data Ecosystem2026-03-07 收录
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https://figshare.com/articles/dataset/Variable_Nitric_Oxide_Reactivity_of_Tropocoronand_Cobalt_III_Nitrite_Complexes_as_a_Function_of_the_Polymethylene_Linker_Chain_Length/2491711
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The size-dependent reactivity of cobalt tropocoronands [TC-n,n]2– is manifest in the NO chemistry of the cobalt­(III) nitrite complexes [Co­(η2-NO2)­(TC-n,n)] (n = 4–6), the synthesis and characterization of which are reported for the first time. Complete conversion of [Co­(η2-NO2)­(TC-4,4)] to the cobalt mononitrosyl [Co­(NO)­(TC-4,4)] occurs upon exposure to NO­(g). In contrast, addition of NO­(g) to [Co­(η2-NO2)­(TC-5,5)] generates both cobalt mono- and dinitrosyl adducts, and addition of nitric oxide to [Co­(η2-NO2)­(TC-6,6)] converts this complex to the dicobalt tetranitrosyl species [Co2(NO)4(TC-6,6)]. In the latter complex, two tetrahedral cobalt dinitrosyl units are bound to the aminotroponeiminate poles of the [TC-6,6]2– ligand. These results significantly broaden the chemistry of cobalt tropocoronands with nitric oxide and the nitrite anion.
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2016-02-20
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