Qualitative and quantitative analysis of intermolecular interactions in xanthenedione derivatives

The existence of intermolecular interactions and the conformational geometry adopted by molecules are related to biological activity. Xanthenedione molecules are promising and emerging antioxidants and acetylcholinesterase inhibitors. To examine the role of different functional groups involved in the intermolecular interactions and conformational geometries adopted in xanthenediones, a series of three substituted xanthenediones have been crystallized [9-(3-hydroxyphenyl)-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1H-xanthene- 1,8(2H)-dione, C<inf>23</inf>H<inf>26</inf>O<inf>4</inf>, 9-(5-bromo-2-methoxyphenyl)-3,3,6,6-tetramethyl- 3,4,6,7-tetrahydro-2H-xanthene-1,8(5H,9H)-dione, C<inf>24</inf>H<inf>27</inf>BrO<inf>4</inf>, and 3,3,6,6- tetramethyl-9-(pyridin-2-yl)-3,4,6,7-tetrahydro-2H-xanthene-1,8(5H,9H)-dione, C<inf>22</inf>H<inf>25</inf>NO<inf>3</inf>] and their intermolecular interactions analyzed via Hirshfeld analysis. The results show that all the derivatives adopt the same structural conformation, where the central ring has a shallow boat conformation and the outer rings have a twisted boat conformation. The intermolecular interactions in the molecules are predominantly O—H…O, C—H…O and π-π interactions. The optimized structures of the derivatives from theoretical B3LYP/6-311G** calculations show a good correlation with the experimental structures. The lattice energy involved in the intermolecular interactions has been explored using PIXELC.