The X-ray crystal structure of N-(1-hexadecyl)-d-gluconamide and powder diffraction studies on its lower and higher homologues (n = 9−18)
✍ Scribed by Christoph André; Peter Luger; Thomas Gutberlet; Dieter Vollhardt; Jürgen-Hinrich Fuhrhop
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 590 KB
- Volume
- 272
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
The crystal structure of N-(1-hexadecyl)-D-gluconamide [a = 4.8072(6) A, b = 46.771(5) A, c = 5.2885(7) ,~, /3 = 94.37(1)°; monoclinic P21, Z = 2] displays the same molecular conformation and the same monolayer packing-arrangement as its lower homologues described previously. This is at seeming variance with most recent CPMAS 13C NMR solid-state investigations describing a bilayer packing. It can be shown that the bilayer arrangement is the result of a kinetically driven crystallisation process, whereas the monolayer packing is the thermodynamically stable polymorph of the title compound. Powder spectra of dried self-assembled layers of N-(1-alkyl)-D-gluconamides showed only one-dimensional order and exhibited at most two periodicities. These could be assigned to a mono-and bilayer arrangement, respectively. Derivatives with long alkyl chains proved to have a smaller tendency towards monolayer assembling than homologues with a short tail.