The reactions of methylamine, dimethylamine, and trimethylamine with TiS 2 were characterized by several techniques. Detailed studies of the intercalation of methylamine demonstrated that the reaction was of the redox-rearrangement type, where the intercalate is best described as (CH 3 NH Ψ 3 ) y (C
Molecular Intercalation of Ammonia into Zirconium Disulfide
β Scribed by Lori A. Brown; William S. Glaunsinger; Michael J. McKelvy
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 172 KB
- Volume
- 147
- Category
- Article
- ISSN
- 0022-4596
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β¦ Synopsis
The intercalation and deintercalation of NH 3 into ZrS 2 has been investigated by evolved gas analysis, thermogravimetric analysis, di4erential scanning calorimetry, vapor pressure measurements, SQID magnetometry, and X-ray powder di4raction. Ammonia intercalation of ZrS 2 , in contrast to other transition metal disul5des (TS 2 ), is predominately a molecular insertion reaction. Only a small amount of NH Ψ 4 (41%) is present in the intercalate, which may be required for intercalation to occur. The small degree of charge transfer can be understood qualitatively within the rigid-band model. The equilibrium intercalate, (NH 3 ) 0.92 ZrS 2 , can be indexed to a 3R, stage-1 structure having an occupied layer expansion (3.17 A s ) in good agreement with other NH 3 +TS 2 intercalation compounds. The guest+guest and guest+host interactions that stabilize the intercalate apparently involve H 2 N+H2NH 3 and H 2 N+H2S hydrogen bonding, respectively. Based on this study, ammoniated ZrS 2 o4ers an excellent model system for probing the structure and properties of molecular guest species in lamellar materials.
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Intercalation of octadecylamine (ODAMIN) into Na montmorillonite based on the ion-dipole interaction was investigated using molecular mechanics and molecular dynamics simulations combined with X-ray powder diffraction. Molecular modeling revealed the interlayer structure of the ODAMIN-montmorillonit
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