Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10031
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dc.contributor.authorRadulovic, Niko-
dc.contributor.authorBogdanovic, Goran A.-
dc.contributor.authorBlagojevic, Polina-
dc.contributor.authorĐekić, Vera-
dc.contributor.authorVukicevic R.-
dc.date.accessioned2021-04-20T14:41:33Z-
dc.date.available2021-04-20T14:41:33Z-
dc.date.issued2011-01-01-
dc.identifier.issn10741542-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10031-
dc.description.abstractX-Ray analyses of 4-(naphthalen-1-ylamino)- 3-nitro-chromen-2-one and 3-nitro-4-phenylamino-chromen- 2-one showed that thementioned compounds crystallize in the space groups P1- (triclinic crystal system; unit cell parameters: a = 8.087(2) Å, b = 9.241(3) Å, c = 10.911(3) Å, α = 93.77(3)°, β = 102.51(3)°, γ = 106.44(2)°, V= 756.4(4) Å 3 and Z = 2) and P2 1 2 1 2 1 (orthorhombic crystal system; unit cell parameters: a = 4.9274(9) Å, b = 14.725(3) Å, c = 17.866(4) Å, α = β = γ = 90°, V = 1296.3(5)Å 3 and Z = 4), respectively. The analyses of crystal structures and gas phase conformations, inferred from single X-ray crystallographic and molecular modeling experiments, respectively, showed that the changes in p delocalization of the farmacoactive formal 3-amino-2-nitro-acrylic acid derivatives might explain the observed significant difference of the antimicrobial and antioxidant activities and spectral properties of two 4-arylamino-3-nitro-coumarin derivatives. © Springer Science+Business Media, LLC 2010.-
dc.relation.ispartofJournal of Chemical Crystallography-
dc.titleCould X-ray analysis explain for the differing antimicrobial and antioxidant activity of two 2-arylamino-3-nitro-coumarins?-
dc.typeArticle-
dc.identifier.doi10.1007/s10870-010-9918-0-
dc.identifier.scopus79955809921-
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