The molecular packing of the hydrocarbon chains of a homologous series of zinc(II) n-alkanoates from chain length, n c = 4-20 inclusive, have been studied using infrared (IR) and solid state 13 C NMR spectroscopy. Odd-even variation, in density and melting point are explained on the basis of odd-eve
Infrared, X-ray and microscopic studies on the room temperature structure of anhydrous lead (II) n-alkanoates
โ Scribed by Henry A. Ellis; Nicole A.S. White; Richard A. Taylor; Paul T. Maragh
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 171 KB
- Volume
- 738
- Category
- Article
- ISSN
- 0022-2860
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โฆ Synopsis
The room temperature structures of a series of even-chain length lead (II) n-alkanoates have been studied using infrared spectroscopy, X-ray diffraction and polarizing light microscopy. Whilst the bonding is the same for both long and short chain compounds, where four carboxylate groups form an unsymmetrical bidentate bond with a lead atom, with possible carboxylate bridging to adjacent lead atoms, at least for the short chain length compounds, the arrangement of hydrocarbon chains within a lamella is different. Both X-ray and microscopic studies show that for short chain compounds, hydrocarbon chains are arranged as bilayers within a lamella and tilted with respect to the lead basal plane. For the long chain compounds, it is proposed that the chains are arranged as a monolayer within a lamella, in an alternating arrangement, and slightly tilted with respect to the lead basal plane. For all the compounds, X-ray data point to a triclinic unit cell containing four molecules per unit cell with P 1 symmetry, and chains oriented along the c axis.
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