Radical-Triggered Chemiluminescence of Phenanthroline Derivatives: An Insight into Radical-Aromatic Interaction.

ABSTRACT: The hitherto unknown influence of 1,10-phenonthroline (1,10-phen) and its derivatives on the weak chemiluminescence (CL) of periodate-peroxide has been investigated, and a novel method for CL catalysis is described. Herein, we have deconvoluted the variation in CL intensity arising from the addition of various derivatives of 1,10-phen. Interestingly, similar derivatives of 1,10-phen show interesting differences in their reactivity toward CL. Electron-withdrawing substituents on 1,10-phen boosted the CL signals, indicating a negative charge buildup on 1,10-phen in the rate-determining step. The 1,10-phen derivatives having substitution at the C5=C6 position resulted in no CL signals due to the blockage of the reactive site. Mechanistic investigations are interpreted in terms of free radical

SUBMITTER: Shah SNA 

PROVIDER: S-EPMC6751721 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature