1996The Journal of Physical ChemistryRequires access

Crystal Structure and Hydrogen-Bonding Characteristics of N,N-Bis(3,5-dimethyl-2-hydroxybenzyl)methylamine, A Benzoxazine Dimer

Joy P. Dunkers, E. A. ZARATE, Hatsuo Ishida

Open publisher page 101 citations

Abstract

The X-ray crystal structure of N, N -bis(3,5-dimethyl-2-hydroxybenzyl)methylamine as a model dimer for benzoxazine-based phenolic resins is presented, and a hydrogen-bonding scheme involving both inter- and intramolecular hydrogen bonding is proposed. Hydrogen bonding of this model dimer is further studied with Fourier transform infrared (FT-IR) spectroscopy in crystalline, quenched, and molten phases as well as in solution. Additional hydrogen-bonding schemes are proposed. These results are compared to results obtained from molecular modeling using a model dimer with a tert -butyl functionality. The preferred conformations of methyl functional trimers are modeled based on preferred dimer conformations.

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The X-ray crystal structure of N, N -bis(3,5-dimethyl-2-hydroxybenzyl)methylamine as a model dimer for benzoxazine-based phenolic resins is presented, and a hydrogen-bonding scheme involving both inter- and intramolecular hydrogen bonding is proposed. Hydrogen bonding of this model dimer is further studied with Fourier transform infrared (FT-IR) spectroscopy in crystalline, quenched, and molten phases as well as in solution. Additional hydrogen-bonding schemes are proposed. These results are compared to results obtained from molecular modeling using a model dimer with a tert -butyl functionality. The preferred conformations of methyl functional trimers are modeled based on preferred dimer conformations.

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Available abstract

The X-ray crystal structure of N, N -bis(3,5-dimethyl-2-hydroxybenzyl)methylamine as a model dimer for benzoxazine-based phenolic resins is presented, and a hydrogen-bonding scheme involving both inter- and intramolecular hydrogen bonding is proposed. Hydrogen bonding of this model dimer is further studied with Fourier transform infrared (FT-IR) spectroscopy in crystalline, quenched, and molten phases as well as in solution. Additional hydrogen-bonding schemes are proposed. These results are compared to results obtained from molecular modeling using a model dimer with a tert -butyl functionality. The preferred conformations of methyl functional trimers are modeled based on preferred dimer conformations.

Key concepts: Dimer, Hydrogen bond, Methylamine, Intramolecular force, Crystal structure, Chemistry, Crystallography, Crystal (programming language)

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Crystal Structure and Hydrogen-Bonding Characteristics of N,N-Bis(3,5-dimethyl-2-hydroxybenzyl)methylamine, A Benzoxazine Dimer — Research Paper | ScholarLens