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Selective Synthesis of Lamellar Titania with Carboxylate Precursor and Characterization by Solid-State NMR

机译:羧酸盐前体选择性合成层状二氧化钛及其固相NMR表征

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摘要

A new means of synthesizing titania mesostructures with ammonium titanyl carboxylates in basic aqueous solution is presented. With a cetyltrimethylammonium bromide (CTAB) ionic template, a lamellar titania was synthesized from an ammonium titanyl oxalate Ti-precursor, and a hexagonally ordered mesoporous titania was synthesized from an ammonium titanyl citrate Ti-precursor. The molecular structure and dynamics of cetyltrimethylammonium (CTA) cations between the lamellar titania layers were studied by solid-state NMR. ~(13)C SP MAS, CP MAS, WISE, and DRSE spectra provided the structural and molecular dynamics information on the CTA cations between the titania layers: (1) bent conformations near the head group, (2) rotation of the methylene carbons in trans conformation about the cetyl chain axes, (3) common rapid methyl group rotation, and (4) interdigitated structures in an antiparallel fashion. The cetyl chains in CTAB are interdigitated as well; however, they are all in trans conformation without any bent. Another difference is that the CTA cations in CTAB have overall lesser mobility than those between the titania layers. The possibility was discussed that the oxalates exist as ligands to the surface Ti of the lamellar titania layers and that the CTA cations interact with the oxalates.
机译:提出了一种在碱性水溶液中与钛氧基羧酸铵合成二氧化钛介观结构的新方法。使用十六烷基三甲基溴化铵(CTAB)离子模板,由草酸钛氧基铵钛前驱体合成层状二氧化钛,并由柠檬酸钛氧基铵钛前驱体合成六方有序介孔二氧化钛。通过固态NMR研究了层状二氧化钛层之间的十六烷基三甲基铵(CTA)阳离子的分子结构和动力学。 〜(13)C SP MAS,CP MAS,WISE和DRSE光谱提供了有关二氧化钛层之间CTA阳离子的结构和分子动力学信息:(1)头基附近的弯曲构象,(2)亚甲基碳的旋转以十六烷基链轴的反式构象,(3)共同的甲基快速旋转,和(4)以反平行方式进行叉指结构。 CTAB中的十六烷基链也相互交叉;然而,它们都是反式构象,没有任何弯曲。另一个区别是CTAB中的CTA阳离子总体上比二氧化钛层之间的迁移率小。讨论了草酸盐作为层状二氧化钛层的表面Ti的配体存在并且CTA阳离子与草酸盐相互作用的可能性。

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