Assignment of the Carbon-Hydrogen Stretching and Bending Vibrations of Poly(Methyl Methacrylate) by Selective Deuteration

1979 ◽  
Vol 33 (6) ◽  
pp. 555-561 ◽  
Author(s):  
Stoil K. Dirlikov ◽  
Jack L. Koenig

The C—H stretching and C—H bending vibrations of the methylene, α-methyl, and ester methyl groups of poly(methyl methacrylate) are discussed and assigned on the basis of the infrared spectra of its three deuterated derivatives: PMMA—CD3—OCD3, PMMA—CD2—OCD3, and PMMA—CD2—CD3. The digital analog of PMMA is obtained by coaddition of the Fourier transform infrared spectra of the deuterated PMMA derivatives. The experimental and digital PMMA spectra are compared in the regions of the C—H stretching and C—H bending vibrations: the agreement in frequency is excellent and the relative intensities are practically the same in the C—H stretching vibrations region. However, their relative intensities strongly differ in the C—H bending region.

1979 ◽  
Vol 33 (6) ◽  
pp. 551-555 ◽  
Author(s):  
Stoil Dirlikov ◽  
Jack L. Koenig

Fourier transform infrared spectrum of atactic poly(methyl methacrylate) (PMMA) is compared with that of atactic PMMA labeled with 18O in the ester groups. The results obtained define the assignment of the bands associated with vibrations of the ester groups of PMMA. Furthermore, the Fourier transform infrared spectroscopy provides a simple method for obtaining the spectra of “pure” derivatives containing 18O.


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