Chandrasekhar, Sosale and Mukherjee, Somnath (2015) Salts of hexamethylenetetramine with organic acids: Enhanced anomeric interactions with a lowering of molecular symmetry revealed by crystal structures. In: JOURNAL OF MOLECULAR STRUCTURE, 1082 . pp. 188-194.
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Abstract
The hexamethylenetetramine (HMT) framework displays interesting stereoelectronic interactions of the anomeric type. In the highly symmetrical parent system, the nitrogen centres act as both donors and acceptors. Protonation lowers symmetry and also leads to an enhancement of the anomeric interaction around the protonated centre. X-ray diffraction crystal structures of four derivatives of HMT - with succinic, (DL)-malic, phthalic and 4-hydroxybenzoic acids - reveal significant trends. (The first three form well-defined salts, 4-hydroxybenzoic acid forming a co-crystalline compound.) Each molecular structure is essentially characterised by a major anomeric interaction involving the protonated centre as acceptor. In two cases (succinic and 4-hydroxybenzoic), secondary protonation leads to a weaker anomeric interaction site that apparently competes with the dominant one. Bond length changes indicate that the anomeric interaction decreases as malic > phthalic > succinic > 4-hydroxybenzoic, which correlates with the degree of proton transfer to the nitrogen centre. Along with other bond length and angle changes, the results offer insight into the applicability of the antiperiplanar lone pair hypothesis (ALPH) in a rigid system. (C) 2014 Elsevier B.V. All rights reserved.
Item Type: | Journal Article |
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Publication: | JOURNAL OF MOLECULAR STRUCTURE |
Publisher: | ELSEVIER SCIENCE BV |
Additional Information: | Copy right for this article belongs to the ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS |
Keywords: | ALPH; Hexamethylenetetraminium; Hydrogen bonding; Stereoelectronic; Urotropine |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 28 Feb 2015 07:08 |
Last Modified: | 28 Feb 2015 07:08 |
URI: | http://eprints.iisc.ac.in/id/eprint/50932 |
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