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Vibrational properties of polysiloxanes: from dimer to oligomers and polymers. 1. Structural and vibrational properties of hexamethyldisiloxane (CH 3 ) 3 SiOSi(CH 3 ) 3
Author(s) -
Carteret C.,
Labrosse A.
Publication year - 2010
Publication title -
journal of raman spectroscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.748
H-Index - 110
eISSN - 1097-4555
pISSN - 0377-0486
DOI - 10.1002/jrs.2537
Subject(s) - hexamethyldisiloxane , chemistry , siloxane , raman spectroscopy , molecule , molecular vibration , infrared , infrared spectroscopy , anharmonicity , molecular geometry , computational chemistry , polymer , organic chemistry , optics , physics , plasma , quantum mechanics
The hexamethyldisiloxane (HMDS)(CH 3 ) 3 SiOSi(CH 3 ) 3 molecule is one of the basic building blocks of silicones and polysiloxanes, as it is used for many chain terminations. Far‐infrared, mid‐infrared, and polarized Raman spectroscopic studies, combined with quantum chemical calculations and vibrational normal mode analyses, were performed for the HMDS molecule. The internal rotation of the trimethylsilyl group was calculated to be nearly free. The large‐amplitude bending motion was found very anharmonic with a barrier to linearity below 4 kJ/mol. Exhaustive assignments of observed wavenumbers have been performed on the basis of calculated potential energy distributions (PED) and atomic displacements. By isotopic 16 O 18 O substitution, the SiOSi symmetric and antisymmetric stretching modes shift from 521 and 1074 cm −1 to 514 and 1028 cm −1 , respectively. This spectroscopic observation provides convincing evidence that the molecule is bent with an angle estimated at around 150°. The comparison of HMDS vibrational spectra with the vibrational spectra of some siloxane derivatives reveals strong effects of silicon substituents on the SiOSi symmetric and antisymmetric stretchings. The SiOSi siloxane bridge group plays a key role in the properties of the HMDS molecule and may also account for some important silicone polymer properties such as their very low glass transition, their high compressibility, and their low surface tension. Copyright © 2009 John Wiley & Sons, Ltd.

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