Infrared studies of sub-monolayer methylamine and trimethylamine adsorption on Ni(111)

The adsorption of monomethylamine and trimethylamine on Ni(111) has been studied using reflection absorption infra-red spectroscopy (RAIRS). At 110 K, both molecules are found to chemisorb molecularly and to retain their gas-phase symmetries at the surface. Methylamine possesses an adsorption site s...

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Published inSurface science Vol. 427; pp. 282 - 287
Main Authors Nunney, T.S., Birtill, J.J., Raval, R.
Format Journal Article Conference Proceeding
LanguageEnglish
Published Lausanne Elsevier B.V 01.06.1999
Amsterdam Elsevier Science
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Abstract The adsorption of monomethylamine and trimethylamine on Ni(111) has been studied using reflection absorption infra-red spectroscopy (RAIRS). At 110 K, both molecules are found to chemisorb molecularly and to retain their gas-phase symmetries at the surface. Methylamine possesses an adsorption site symmetry of C s in which the NH 2 unit is held parallel to the surface plane and the methyl group is tilted with respect to the surface normal. Trimethylamine possesses C 3v symmetry upon adsorption, with the c 3 axis aligned along the surface normal. The high sensitivity RAIR data allow a peculiar feature of methylamines to be probed: the lone pair on the nitrogen gives rise to inequivalence in the CH bonds of the methyl unit, leading to the creation of one much weaker C–H bond that produces a decoupled vibration at an unusually low stretching frequency.
AbstractList The adsorption of monomethylamine and trimethylamine on Ni(111) has been studied using reflection absorption infra-red spectroscopy (RAIRS). At 110 K, both molecules are found to chemisorb molecularly and to retain their gas-phase symmetries at the surface. Methylamine possesses an adsorption site symmetry of C s in which the NH 2 unit is held parallel to the surface plane and the methyl group is tilted with respect to the surface normal. Trimethylamine possesses C 3v symmetry upon adsorption, with the c 3 axis aligned along the surface normal. The high sensitivity RAIR data allow a peculiar feature of methylamines to be probed: the lone pair on the nitrogen gives rise to inequivalence in the CH bonds of the methyl unit, leading to the creation of one much weaker C–H bond that produces a decoupled vibration at an unusually low stretching frequency.
Author Nunney, T.S.
Birtill, J.J.
Raval, R.
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Keywords Chemisorption
Methylamines
Nickel
Single crystal surfaces
Reflection absorption IR spectroscopy
Vibrations of adsorbed molecules
Gas solid adsorption
Amine
Organic adsorbate
Gas solid interface
Metallic adsorbent
Transition metal
Infrared spectrum
Experimental study
Vibrational mode
Language English
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Snippet The adsorption of monomethylamine and trimethylamine on Ni(111) has been studied using reflection absorption infra-red spectroscopy (RAIRS). At 110 K, both...
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SubjectTerms Chemisorption
Chemistry
Condensed matter: structure, mechanical and thermal properties
Dynamics; vibrations
Exact sciences and technology
General and physical chemistry
Methylamines
Nickel
Physics
Reflection absorption IR spectroscopy
Single crystal surfaces
Solid-fluid interfaces
Solid-gas interface
Surface and interface dynamics and vibrations
Surface physical chemistry
Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties)
Vibrations of adsorbed molecules
Title Infrared studies of sub-monolayer methylamine and trimethylamine adsorption on Ni(111)
URI https://dx.doi.org/10.1016/S0039-6028(99)00280-0
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