Preparation of a novel organic derivative of the layered perovskite bearing HLaNb2O7.nH2O interlayer surface trifluoroacetate groups
- 1. Department of Applied Chemistry, School of Science and Engineering, Waseda University, Ohkubo-3, Shinjuku-ku, Tokyo 169-8555 (Japan)
Description
Trifluoroacetate (TFA, CF3COO) groups have been successfully bound to the interlayer surface of a protonated form of Dion-Jacobson-type layered perovskite, HLaNb2O7.nH2O (HLaNb), via a reaction between its n-propoxy derivative and trifluoroacetic acid (TFAH, CF3COOH). The interlayer distance increases approximately to 1.8 nm upon treatment with TFAH, and varies in the range from ∼1.7 to ∼2.0 nm depending on the amount of water adsorbed in the interlayer space. The high stability of the guest species upon dispersal in organic solvents and the change in the infrared (IR) spectrum profile with respect to that of TFAH indicate that the guest species are TFA groups bound to the surface of perovskite-like slabs of HLaNb. The interlayer distance indicates that the TFA groups possess a bilayer arrangement, and a unidentate type of coordination is proposed based on consideration on the coordination geometry
Additional details
Identifiers
- DOI
- 10.1016/j.materresbull.2005.10.004;
- PII
- S0025-5408(05)00379-X;
Publishing Information
- Journal Title
- Materials Research Bulletin
- Journal Volume
- 41
- Journal Issue
- 4
- Journal Page Range
- p. 834-841
- ISSN
- 0025-5408
- CODEN
- MRBUAC
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38056206
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CHEMICAL PREPARATION; INFRARED SPECTRA; NUCLEAR MAGNETIC RESONANCE; ORGANIC SOLVENTS; PEROVSKITE; SLABS; STABILITY; SURFACE PROPERTIES; X-RAY DIFFRACTION
- Descriptors DEC
- COHERENT SCATTERING; DIFFRACTION; MAGNETIC RESONANCE; MINERALS; NONAQUEOUS SOLVENTS; OXIDE MINERALS; PEROVSKITES; RESONANCE; SCATTERING; SOLVENTS; SPECTRA; SYNTHESIS
Optional Information
- Copyright
- Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.