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Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units.

ABSTRACT: A synthetic approach to a new group of stable chiral C2-symmetric diimines with the 4,5-diazafluorene core has been developed based on condensation of dipinodiazafluorene with aromatic diamines. The chemical structures of new compounds were proven by spectroscopic methods and X-ray crystallography. All the compounds form solvates with organic solvents (chloroform, benzene, 1,4-dioxane) and water. Specific spectral data of the new compounds are explained using calculated data (DFT). Diimines of the pinodiazafluorene series give colored reactions with transition metal ions and can be regarded as prospective polydentate ligands with interesting luminescent and chiroptical properties.

SUBMITTER: Vasilyev ES

PROVIDER: S-EPMC6749561 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units.

Vasilyev Eugene S ES Bizyaev Sergey N SN Komarov Vladislav Yu VY Gatilov Yury V YV Tkachev Alexey V AV

Molecules (Basel, Switzerland) 20190902 17

A synthetic approach to a new group of stable chiral C2-symmetric diimines with the 4,5-diazafluorene core has been developed based on condensation of dipinodiazafluorene with aromatic diamines. The chemical structures of new compounds were proven by spectroscopic methods and X-ray crystallography. All the compounds form solvates with organic solvents (chloroform, benzene, 1,4-dioxane) and water. Specific spectral data of the new compounds are explained using calculated data (D ...[more]

PMID: 31480760

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