Relative influence of noncovalent interactions on the melting points of a homologous series of 1, 2‐dibromo‐4, 5‐dialkoxybenzenes. (5th February 2013)

• Record Type: Journal Article
• Authors: Fonrouge, Ana; Cecchi, Florencia; Alborés, Pablo; Baggio, Ricardo; Cukiernik, Fabio D.
• Is Part Of: Acta crystallographica. Volume 69:Part 2(2013:Feb.)
• Page Start: 204
• Page End: 208
• Publication Date: 2013-02-05
• Subjects: Crystallography -- Periodicals; Crystals -- Periodicals; 548.05
• DOI: 10.1107/S0108270113002485
• Languages: English
• ISSNs: 0108-2701

Abstract

Abstract : Crystal structures are presented for two members of the homologous series of 1, 2‐dibromo‐4, 5‐dialkoxybenzenes, viz. those with decyloxy and hexadecyloxy substituents, namely 1, 2‐dibromo‐4, 5‐bis(decyloxy)benzene, C26 H44 Br2 O2, (II), and 1, 2‐dibromo‐4, 5‐bis(hexadecyloxy)benzene, C38 H68 Br2 O2, (III). The relative influences which halogen bonding, π–π stacking and van der Waals interactions have on these structures are analysed and the results compared with those already found for the lightest homologue, 1, 2‐dibromo‐4, 5‐dimethoxybenzene, (I) [Cukiernik, Zelcer, Garland & Baggio (2008). Acta Cryst. C64, o604–o608]. The results confirm that the prevalent interactions stabilizing the structures of (II) and (III) are van der Waals contacts between the aliphatic chains. In the case of (II), weak halogen C—Br...(Br—C)′ interactions are also present and contribute to the stability of the structure. In the case of (III), van der Waals interactions between the aliphatic chains are almost exclusive, weaker C—Br...π interactions being the only additional interactions detected. The results are in line with commonly accepted models concerning trends in crystal stability along a homologous series (as measured by their melting points), but the earlier report for n = 1, and the present report for n = 10 and 16, are among the few providing single‐crystal information validating the hypothesis.