Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/124055
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Type: Journal article
Title: A theoretical study of propagation rate coefficients for methacrylonitrile and acrylonitrile
Author: Huang, D.
Monteiro, M.
Gilbert, R.
Citation: Macromolecules, 1998; 31(16):5175-5187
Publisher: American Chemical Society
Issue Date: 1998
ISSN: 0024-9297
1520-5835
Statement of
Responsibility: 
David M. Huang, Michael J. Monteiro, and Robert G. Gilbert
Abstract: The propagation rate coefficients for methacrylonitrile (MAN) and acrylonitrile (AN) were calculated using transition state theory and high-level ab initio molecular orbital theory. The calculations take particular account of internal rotations in the transition states. Frequency factors and rotational potentials were found to be insensitive to the level of theory used (except that the semiempirical AM1 method does not perform very well), because of cancellations in the partition function ratio in transition state theory; however, two of the internal rotations studied were found to be sensitive to the chain length of the radical used in the calculations. Activation energies were found to be extremely sensitive to the level of theory. At the highest level of theory used, the calculated frequency factor for MAN was slightly lower than experiment, while the activation energy was 2.6 kJ mol⁻¹ higher than experiment. Theoretical comparison of propagation of MAN and AN was used to explain differences observed experimentally in activation energies and frequency factors of methacrylates and corresponding acrylates. The higher frequency factors for methacrylates are largely due to hindrance caused by the methyl groups to the three transitional modes in the transition state which correspond to the three external rotational degrees of freedom of the monomer in the reactants (but not a result of increased hindrance to methyl rotation itself in the transition state). The higher activation energies of methacrylates arises from differences in hindrance and loss of delocalization in the transition states of the methyl-substituted and unsubstituted monomers.
Description: Published on Web 07/22/1998
Rights: © 1998 American Chemical Society
RMID: 0030009445
DOI: 10.1021/ma980229n
Appears in Collections:Chemistry and Physics publications

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