Identification of Intercalates and Grafted Organic Derivatives of H.sub.2La.sub.2Ti.sub.3O.sub.10 by Multinuclear NMR
Using .sup.1H, .sup.13C, and .sup.15N NMR method, it was established that the formation of organic-inorganic hybrids of H.sub.2La.sub.2Ti.sub.3O.sub.10 with methylamine and butylamine produces intercalated alkylamino cations, while the introduction of methanol into the interlayer space of H.sub.2La....
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Published in: | Russian journal of general chemistry Vol. 90; no. 4; p. 760 |
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Abstract | Using .sup.1H, .sup.13C, and .sup.15N NMR method, it was established that the formation of organic-inorganic hybrids of H.sub.2La.sub.2Ti.sub.3O.sub.10 with methylamine and butylamine produces intercalated alkylamino cations, while the introduction of methanol into the interlayer space of H.sub.2La.sub.2Ti.sub.3O.sub.10 is accompanied by the formation of covalent bonds. |
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AbstractList | Using .sup.1H, .sup.13C, and .sup.15N NMR method, it was established that the formation of organic-inorganic hybrids of H.sub.2La.sub.2Ti.sub.3O.sub.10 with methylamine and butylamine produces intercalated alkylamino cations, while the introduction of methanol into the interlayer space of H.sub.2La.sub.2Ti.sub.3O.sub.10 is accompanied by the formation of covalent bonds. |
Audience | Academic |
Author | Zvereva, I. A Lushpinskaya, I. P Silyukov, O. I Shelyapina, M. G Kurnosenko, S. A |
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Copyright | COPYRIGHT 2020 Springer |
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DOI | 10.1134/S1070363220040337 |
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Snippet | Using .sup.1H, .sup.13C, and .sup.15N NMR method, it was established that the formation of organic-inorganic hybrids of H.sub.2La.sub.2Ti.sub.3O.sub.10 with... |
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Title | Identification of Intercalates and Grafted Organic Derivatives of H.sub.2La.sub.2Ti.sub.3O.sub.10 by Multinuclear NMR |
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