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• W3196961575 endingPage "5302" @default.
• W3196961575 startingPage "5302" @default.
• W3196961575 abstract "The reaction of rhenium α-diimine (N-N) tricarbonyl complexes with nitrosonium tetrafluoroborate yields the corresponding dicarbonyl-nitrosyl [Re(CO)2(NO)(N-N)X]+ species (where X = halide). The complexes, accessible in a single step in good yield, are structurally nearly identical higher charge congeners of the tricarbonyl molecules. Substitution chemistry aimed at the realization of equivalent dicationic species (intended for applications as potential antimicrobial agents), revealed that the reactivity of metal ion in [Re(CO)2(NO)(N-N)X]+ is that of a hard Re acid, probably due to the stronger π-acceptor properties of NO+ as compared to those of CO. The metal ion thus shows great affinity for π-basic ligands, which are consequently difficult to replace by, e.g., σ-donor or weak π-acids like pyridine. Attempts of direct nitrosylation of α-diimine fac-[Re(CO)3]+ complexes bearing π-basic OR-type ligands gave the [Re(CO)2(NO)(N-N)(BF4)][BF4] salt as the only product in good yield, featuring a stable Re-FBF3 bond. The solid state crystal structure of nearly all molecules presented could be elucidated. A fundamental consequence of the chemistry of [Re(CO)2(NO)(N-N)X]+ complexes, it that the same can be photo-activated towards CO release and represent an entirely new class of photoCORMs." @default.
• W3196961575 created "2021-09-13" @default.
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• W3196961575 date "2021-08-31" @default.
• W3196961575 modified "2023-09-26" @default.
• W3196961575 title "Efficient Direct Nitrosylation of α-Diimine Rhenium Tricarbonyl Complexes to Structurally Nearly Identical Higher Charge Congeners Activable towards Photo-CO Release" @default.
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• W3196961575 doi "https://doi.org/10.3390/molecules26175302" @default.
• W3196961575 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8434269" @default.
• W3196961575 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34500734" @default.
• W3196961575 hasPublicationYear "2021" @default.
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