A New and Convenient Synthesis of Amino-phthalimide (1H-Isoindole-1,3(2H)-dione) Derivatives and Their Photo luminescent Properties
Özet
A new and convenient synthesis for amino-phthalimide (1H-isoindole-1,3(2H)-dione) derivatives has been developed starting from an alpha, beta-unsaturated ketone. The ketones were reacted with amines to give aromatic amine products. This is the first time that substituted amine groups have been incorporated in aromatic rings. The mechanism of the product formation is rationalized by the 1,2-addition of amines to ketones. All aromatic compounds exhibited high fluorescence properties at the blue-green region.
Atıf için künye
Tan, A., Bozkurt, E., Horasan, N., & Kara, Y. (2014). A New and Convenient Synthesis of Amino-phthalimide (1H-Isoindole-1,3(2H)-dione) Derivatives and Their Photo luminescent Properties. HELVETICA CHIMICA ACTA, 97(8), 1107–1114. https://doi.org/10.1002/hlca.201300394
BibTeX
@article{tan2014-71894,
author = {Tan, Ayse and Bozkurt, Ebru and Horasan, Nurhan and Kara, Yunus},
title = {A New and Convenient Synthesis of Amino-phthalimide (1H-Isoindole-1,3(2H)-dione) Derivatives and Their Photo luminescent Properties},
journal = {HELVETICA CHIMICA ACTA},
year = {2014},
volume = {97},
number = {8},
pages = {1107--1114},
issn = {0018-019X},
doi = {10.1002/hlca.201300394},
url = {https://akademik.atauni.edu.tr/yayinlar/71894-a-new-and-convenient-synthesis-of-amino-phthalimide-1h-isoindole-132h-dione}
}