Azomethine diselenides: Supramolecular structures and facile formation of a bis-oxazoline diselenide

Panda, Snigdha; Dutta, Pradip Kr.; Ramakrishna, Gujjula V; Reddy, C. Malla; Zade, Sanjio S.

doi:10.1016/j.jorganchem.2012.07.026

Cited by 9 publications

(1 citation statement)

References 25 publications

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“…However, a CSD search on phenyl-Se-Se-phenyl compounds gave 152 hits and 199 observations with the Se-Se distance ranging from 2.287 to 3.051 A ˚(with a mean value of 2.393 A ˚and a standard deviation 0.162). In the structures of CATWEB01, REDGAK, REDGEO and REDGUE (Panda et al, 2012), the typical torsional angles of the selenium-attached phenyl ring (C-Se-Se-C) are ca 81 and those of CIDXET and CIDXUJ (Kulcsar et al, 2007) are 80.9 and 114.0 , respectively.…”

Section: Database Surveymentioning

confidence: 99%

Crystal structure, Hirshfeld surface analysis and DFT study of 2,2′′-({[(1E,1′E)-(diselanediyl)bis(2,1-phenylene)]bis(methaneylylidene)}bis(azaneylylidene))bis[3′,6′-bis(diethylamino)-4a',9a'-dihydrospiro[isoindoline-1,9′-xanthen]-3-one]

et al. 2022

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The title compound, C70H70N8O4Se2, is a spiro bicyclic diselenide, made up of two [SeC6H4CH=N—N(CO)C6H4(C)C6H3NEt2(O)C6H3NEt2] units related by a twofold crystallographic symmetry element bisecting the diselenide bond. The compound crystallizes in a non-centrosymmetric polar space group (tetragonal, P\overline{4}b2) and the structure was refined as an inversion twin. The two diethyl amine groups and their attached phenyl groups of the xanthene ring are disordered over two orientations, with occupancies of 0.664 (19)/0.336 (19) and 0.665 (11)/0.335 (11), respectively. The dihedral angles between the mean planes of the central isoindoline and the phenyl rings are 26.8 (2) and 2.5 (4)°, respectively. The mean plane of the central xanthene ring forms dihedral angles of 2.0 (5), 8.8 (5), 1.7 (5) and 7.9 (6)° with the peripheral phenyl rings. The isoindoline and xanthene rings subtend a dihedral angle of 89.8 (2)°. The molecular conformation is stabilized by an intramolecular C—H...O hydrogen bond generating an S(6) ring motif. In the crystal, molecules are linked by C—H...O hydrogen bonds together with C—H...π (ring) interactions, forming a three-dimensional network. A Hirshfeld surface analysis of the crystal structure indicates that the most important contributions to the crystal packing are from H...H (68.1%), C...H/H...C (21.2%) and O...H/H...O (8.7%) contacts. The optimized structure calculated using density functional theory (DFT) at the B3LYP/6 – 31 G(d) level is compared with the experimentally determined molecular structure in the solid state. The HOMO–LUMO behaviour was used to determine the energy gap and the molecular electrostatic potential (MEP) of the compound was investigated.

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Section: Database Surveymentioning

confidence: 99%