Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3208
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dc.contributor.authorRAO, GUDIPATI SRINIVASA-
dc.contributor.authorBASAVOJU, SRINIVAS-
dc.contributor.authorA, RAMACHANDRAIAH-
dc.date.accessioned2025-02-06T09:53:19Z-
dc.date.available2025-02-06T09:53:19Z-
dc.date.issued2014-
dc.identifier.citation10.1080/15421406.2014.905033en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3208-
dc.descriptionNITWen_US
dc.description.abstractA novel Betti base compound, 1-((2-hydroxynaphthalen-1-yl)(2-hydroxyphenyl) methyl)urea, UBB, was synthesized and characterized by spectral, structural and thermal studies. Single crystal X-ray diffraction studies reveal that the racemic mixture of the compound, when crystallized from DMF, yields R-isomer preferentially (prismatic crystals), whereas, when crystallized from 5:1 (v/v) mixture of DMF-THF, it yields Sisomer (rectangular shaped crystals) with two molecules of DMF, included in both the cases. The crystal structure is discussed in terms of supramolecular interactions and molecular modeling. Both R and S enantiomeric DMF solvate crystals are in their chiral triclinic P1 space group.en_US
dc.language.isoenen_US
dc.publisherMolecular Crystals and Liquid Crystalsen_US
dc.subject1-((2-hydroxynaphthalen-1-yl)(2-hydroxyphenyl)methyl)ureaen_US
dc.subjectThermal analysis.en_US
dc.titleCrystal structure analysis of betti base 1-((2-hydroxynaphthalen-1-yl)(2-hydroxyphenyl)methyl)urea•2DMF solvateen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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