Crystal structure of 1,1′-{(1E,1′E)-[4,4′-(9H-fluorene-9,9-diyl)bis(4,1-phenylene)]bis(azanylylidene)bis(methanylylidene)}bis(naphthalen-2-ol) dichlorobenzene monosolvate

Acta Crystallographica Section E: Crystallographic Communications

Ayalew Wodajo¹  Tuan Anh Le²  Alexey S. Kubasov³  Alexander G. Tskhovrebov⁴  Oleg N. Krutius⁴  Maria M. Grishina⁵  Victor N. Khrustalev⁵ 

[1] College of Natural and Computational Sciences, University of Gondar, 196 Gondar, Ethiopia;Faculty of Chemistry, VNU University of Science, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam;Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninsky Prosp. 31, Moscow, Russian Federation;N. N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Ul. Kosygina 4, Moscow, Russian Federation;Peoples Friendship University of Russia, 6 Miklukho-Maklaya Street, Moscow, 117198, Russian Federation;

关键词: azomethines;    imines;    hydrogen bonding;    weak interactions;    excited-state intramolecular proton transfer;    crystal structure;   

DOI  :  10.1107/S2056989020012104

来源: DOAJ

【 摘 要 】

The bis(anil) molecule of the title compound, C47H32N2O2·C6H4Cl2, contains two anil fragments in the enol–enol form, exhibiting intramolecular O—H...N hydrogen bonds. The two hydroxynaphthalene ring systems are approximately parallel to each other with a dihedral angle of 4.67 (8)° between them, and each ring system makes a large dihedral angle [55.11 (11) and 48.50 (10)°] with the adjacent benzene ring. In the crystal, the bis(anil) molecules form an inversion dimer by a pair of weak C—H...O interactions. The dimers arrange in a one-dimensional column along the b axis via another C—H...O interaction and a π–π stacking interaction between the hydroxynaphthalene ring system with a centroid–centroid distance of 3.6562 (16) Å. The solvent 1,2-dichlorobenzene molecules are located between the dimers and bind neighbouring columns by weak C—H...Cl interactions. Theoretical prediction of potential biological activities was performed, which suggested that the title anil compound can exhibit histone deacetylase SIRT2, histone deacetylase class III and histone deacetylase SIRT1 activities, and will act as inhibitor to aspulvinone dimethylallyltransferase, dehydro-l-gulonate decarboxylase and glutathione thiolesterase.

【 授权许可】

Unknown