Title of article :
Synthesis and structure of push–pull merocyanines based on barbituric and thio­barbituric acid
Author/Authors :
Bogdanov, Georgii Department of Chemistry- New Mexico Highlands University, USA , Tillotson, John P. School of Chemistry and Biochemistry - Georgia Institute of Technology, USA , Bustos, Jenna Department of Chemistry- New Mexico Highlands University, USA , Timofeeva, Tatiana V. Department of Chemistry- New Mexico Highlands University, USA
Pages :
15
From page :
1
To page :
15
Abstract :
Two compounds, 1,3-diethyl-5-{(2E,4E)-6-[(E)-1,3,3-tri­methyl­indolin-2-yl­idene]hexa-2,4-dien-1-yl­idene}pyrimidine-2,4,6(1H,3H,5H)-trione or TMI, C25H29N3O3, and 1,3-diethyl-2-sulfanyl­idene-5-[2-(1,3,3-tri­methyl­indolin-2-yl­idene)ethyl­idene]di­hydro­pyrimidine-4,6(1H,5H)-dione or DTB, C21H25N3O2S, have been crystallized and studied. These compounds contain the same indole derivative donor group and differ in their acceptor groups (in TMI it contains oxygen in the para position, and in DTB sulfur) and the length of the π-bridge. In both materials, mol­ecules are packed in a herringbone manner with differences in the twist and fold angles. In both structures, the mol­ecules are connected by weak C—H⋯O and/or C—H⋯S bonds.
Keywords :
crystal structure , barbituric acid derivatives , push–pull chromophores
Journal title :
Acta Crystallographica Section E: Crystallographic Communications
Serial Year :
2019
Full Text URL :
Record number :
2625299
Link To Document :
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