Title : Reactivity of biomimetic iron(II)-2-aminophenolate complexes toward dioxygen: mechanistic investigations on the oxidative C-C bond cleavage of substituted 2-aminophenols.

Pub. Date : 2014 May 19

PMID : 24787025






2 Functional Relationships(s)
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1 The presence of two tert-butyl groups on the aminophenolate ring in 7 ClO4 makes the complex slow to cleave the C-C bond of 4,6-di-(t)Bu-HAP, whereas 4 BPh4 containing 4-Me-HAP displays fastest reactivity. perchlorate reticulon 3 Homo sapiens
2 The presence of two tert-butyl groups on the aminophenolate ring in 7 ClO4 makes the complex slow to cleave the C-C bond of 4,6-di-(t)Bu-HAP, whereas 4 BPh4 containing 4-Me-HAP displays fastest reactivity. perchlorate reticulon 3 Homo sapiens