Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/26497
Title: Microwave synthesis, crystal structure and spectroscopic investigations of 2-{[(2E)-(2-chlorobenzylidene) hydrazine] carbonyl} benzenesulfonamide and 2-({[(2E)-2-[4-(dimethylamino) benzylidene] hydrazine} carbonyl) benzenesulfonamide
Authors: Thiyagarajan, G
Pandey, Ashutosh
Mayer, Peter
Thamaraichelvan, A
Keywords: Hydrazine;Benzenesulfonamide;Crystallography;Microwave synthesis;Condensation
Issue Date: Feb-2014
Publisher: NISCAIR-CSIR, India
Abstract: The compounds 2-{[(2E)-(2-chlorobenzylidene) hydrazine] carbonyl} benzenesulfonamide 5a and 2-({[(2E)-2-[4-(dimethylamino)benzylidene] hydrazine} carbonyl) benzenesulfonamide 5b have been synthesized by microwave heating and characterized by NMR, FT-IR and single crystal X-ray crystallography. They have been obtained in higher yields in lesser reaction times through microwave irradiation. (C14H12ClN3O3S, 5a): MW = 337.782, triclinic, Pī,  a = 7.8804(7) Å, b = 11.5285(11) Å, c = 18.1620 (19) Å, α = 89.452(7)°, β = 76.847(8)°, γ = 75.999(8)°, V = 1557.2(3) Å3, Z = 4; (C16H20N4O4S, 5b): MW = 364.421, Orthorhombic, P212121, a = l,6.5693(2) Å, b = 7.0856(3) Å, c = 37.8187(15) Å, α = 90°, β = 90°, γ = 90°, V = 1760.36(12) Å3, Z = 4. The delocalizations as well as the presence of the intra-molecular hydrogen bonding in 5a and 5b lead to the planarity of the benzene rings. There are π-π stacking interactions among the adjacent aromatic systems in both the compounds. It is also anticipated that the synchronized effect of both benzenesulfonamide and hydrazone groups in 5a and 5b should make them potential candidates for biological applications.
Page(s): 200-207
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.53B(02) [February 2014]

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