Somchai KeawwangchaiThawatchai TuntulaniVithaya RuangpornvisutiMahidol University2018-08-242018-08-242007-04-30Journal of Molecular Structure. Vol.832, No.1-3 (2007), 16-25002228602-s2.0-33847644032https://repository.li.mahidol.ac.th/handle/123456789/24359The optimized structures of the 3,6-di(hexylthioureido)acridine conformers were obtained using density functional theory (DFT) and ONIOM methods. Three conformers of 3,6-di(hexylthioureido)acridine and their corresponding protonated forms were found. Single-point energies calculations were obtained using second-order Møller-Plesset at the MP2(fc)/6-31G(d) level. The computed1H NMR chemical shifts referenced to TMS in DMSO for all conformers were obtained. The presence of symmetrical conformers of the neutral and protonated structures were confirmed by the1H NMR measurement. The measured and computed IR spectra of the neutral and protonated species of 3,6-di(hexylthioureido)acridine were obtained and compared. © 2006 Elsevier B.V. All rights reserved.Mahidol UniversityChemistryArticleSCOPUS10.1016/j.molstruc.2006.07.039