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- W2086135051 abstract "Non-heme Fe(II) proteins form stable nitrosyl adducts. However, there are few synthetic examples of structurally characterized non-heme iron nitrosyl complexes, especially those that are coordinatively unsaturated. Presented herein is a series of non-heme {Fe−NO}7 complexes with trigonal bipyramidal coordination geometry. These complexes were synthesized with tripodal ligands derived from tris(N-R-carbamoylmethy)amine [1R]3- where R = isopropyl (iPr), cyclopentyl (cyp), or 3,5-dimethylphenyl (dmp) groups. The R groups of these [1R]3- ligands form cavities around the metal ion that can influence structural and functional properties. The nitrosyl complexes were synthesized by treating the Fe(II) precursors [Fe1R]- with NO at room temperature. These iron nitrosyl complexes have similar molecular structures as determined by X-ray diffraction methods. They differ in their Fe−N−O angles which range from 178.2(5)° in [Fe1iPr(NO)]- to 160.3(2)° in [Fe1dmp(NO)]-. The observed difference in angle is related to the cavity size: [Fe1iPr(NO)]- has the most restricted cavity with a small diameter (∼ 3 Å) while [Fe1dmp(NO)]- is more flexible and larger (∼8 Å diameter). This angular difference is supported by EPR measurements which shows that [Fe1dmp(NO)]- has a significantly more rhombic spectrum than that found for [Fe1iPr(NO)]-. Magnetic moment, Mössbauer and EPR data on these {Fe−NO}7 complexes agree with a electronic configuration of [Fe3+ d5 HS (S = 5/2)−NO- (S = 1)] that lead to an S = 3/2 ground state via antiferromagnetic coupling." @default.
- W2086135051 created "2016-06-24" @default.
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- W2086135051 date "1999-05-29" @default.
- W2086135051 modified "2023-10-03" @default.
- W2086135051 title "Structure and Magnetic Properties of Trigonal Bipyramidal Iron Nitrosyl Complexes" @default.
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- W2086135051 doi "https://doi.org/10.1021/ic990070a" @default.
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