Published April 13, 2006 | Version v1
Journal article

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.