Carbon number-dependent intercalation and interlayer amidation properties of α,ω-alkanediamines for α-titanium (2-carboxyethyl)phosphonate phosphate

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Tsuyoshi Kijima, Masa-aki Yamaguchi, Kiyohiko Imaizumi, Mitsunori Yada and Masato Machida


Abstract

The uptake of α,ω-alkanediamines H2N(CH2)nNH2 (n = 2–10) by α-titanium (2-carboxyethyl)phosphonate phosphate, Ti(O3PCH2CH2CO2H)1.91(HPO4)0.09, has been studied at 25 °C. Each diamine forms one or two intercalated phases in which the amine molecules are arranged as a monolayer with their axes tilted by 54 or 67° relative to the inorganic layer. Diamines with n [greater than or equal, slant] 7 show a tendency to produce the high and low chain-tilt forms depending on the even and odd number of carbon atoms, respectively, but both forms coexist for n = 6. For shorter chain diamines, on the other hand, only the low-tilt form occurs for n = 3, 4 and 5 and the high-tilt form for n = 2. On heating at 150 °C or above the diammonium-exchanged solids were thermally condensed into the amide form with or without any significant release of the amine guest. The amidation temperature shows a tendency to vary up or down depending on whether the carbon number is even or odd.


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