Chiral C2-symmetric diimines with 4,5-diazafluorene units

Standard

Chiral C₂-symmetric diimines with 4,5-diazafluorene units. / Vasilyev, Eugene S.; Bizyaev, Sergey N.; Komarov, Vladislav Yu et al.

In: Molecules, Vol. 24, No. 17, 3186, 02.09.2019.

Research output: Contribution to journal › Article › peer-review

Harvard

Vasilyev, ES, Bizyaev, SN, Komarov, VY, Gatilov, YV & Tkachev, AV 2019, 'Chiral C₂-symmetric diimines with 4,5-diazafluorene units', Molecules, vol. 24, no. 17, 3186. https://doi.org/10.3390/molecules24173186

APA

Vasilyev, E. S., Bizyaev, S. N., Komarov, V. Y., Gatilov, Y. V., & Tkachev, A. V. (2019). Chiral C₂-symmetric diimines with 4,5-diazafluorene units. Molecules, 24(17), [3186]. https://doi.org/10.3390/molecules24173186

Vancouver

Vasilyev ES, Bizyaev SN, Komarov VY, Gatilov YV, Tkachev AV. Chiral C₂-symmetric diimines with 4,5-diazafluorene units. Molecules. 2019 Sept 2;24(17):3186. doi: 10.3390/molecules24173186

Author

Vasilyev, Eugene S. ; Bizyaev, Sergey N. ; Komarov, Vladislav Yu et al. / Chiral C₂-symmetric diimines with 4,5-diazafluorene units. In: Molecules. 2019 ; Vol. 24, No. 17.

BibTeX

@article{2bb64990e68a44f2b4942a7d0fcaf877,

title = "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.",

keywords = "4,5-diazafluorenon-9-one, Aromatic diamines, Chiral dipinodiazafluorenone, Pinocarvone oxime, Stable chiral diimines, pinocarvone oxime, stable chiral diimines, chiral dipinodiazafluorenone, aromatic diamines",

author = "Vasilyev, {Eugene S.} and Bizyaev, {Sergey N.} and Komarov, {Vladislav Yu} and Gatilov, {Yury V.} and Tkachev, {Alexey V.}",

note = "Publisher Copyright: {\textcopyright} 2019 by the authors.",

year = "2019",

month = sep,

day = "2",

doi = "10.3390/molecules24173186",

language = "English",

volume = "24",

journal = "Molecules",

issn = "1420-3049",

publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",

number = "17",

}

RIS

TY - JOUR

T1 - Chiral C2-symmetric diimines with 4,5-diazafluorene units

AU - Vasilyev, Eugene S.

AU - Bizyaev, Sergey N.

AU - Komarov, Vladislav Yu

AU - Gatilov, Yury V.

AU - Tkachev, Alexey V.

PY - 2019/9/2

Y1 - 2019/9/2

N2 - 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.

AB - 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.

KW - 4,5-diazafluorenon-9-one

KW - Aromatic diamines

KW - Chiral dipinodiazafluorenone

KW - Pinocarvone oxime

KW - Stable chiral diimines

KW - pinocarvone oxime

KW - stable chiral diimines

KW - chiral dipinodiazafluorenone

KW - aromatic diamines

UR - http://www.scopus.com/inward/record.url?scp=85071736156&partnerID=8YFLogxK

U2 - 10.3390/molecules24173186

DO - 10.3390/molecules24173186

M3 - Article

C2 - 31480760

AN - SCOPUS:85071736156

VL - 24

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 17

M1 - 3186

ER -

ID: 21465716