Volume 101, Issue 5 pp. 3462-3467

Poly(1,3-disila-1,3-diphenyl-2-oxaindane)-diphenylsiloxane-poly(dimethylsiloxane) block copolymers

O. Mukbaniani

Corresponding Author

O. Mukbaniani

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia===Search for more papers by this author
M. Matsaberidze

M. Matsaberidze

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia

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V. Achelashvili

V. Achelashvili

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia

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N. Mukbaniani

N. Mukbaniani

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia

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A. Samsonia

A. Samsonia

Iv. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue, 1, Tbilisi 0128, Republic of Georgia

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First published: 22 June 2006
Citations: 2

Abstract

The heterofunctional condensation of 1,3-dichloro-1,3-disila-1,3-diphenyl-2-oxaindane with dihydroxydiphenylsilane at various ratios of initial compounds in the presence of amines was carried out, and α,ω-dihydroxy(1,3-disila-1,3-diphenyl-2-oxaindane)-diphenylsiloxane oligomers with various degrees of condensation were obtained. Corresponding block copolymers were obtained by heterofunctional polycondensation of synthesized α,ω-dihydroxy(1,3-disila-1,3-diphenyl-2-oxaindane)-diphenylsiloxane oligomers with α,ω-dichlorodimethylsiloxanes in the presence of amines. Thermogravimetry, gel permeation chromatography, differential scanning calorimetry, and wide-angle X-ray analysis were carried out on the synthesized block coplymers. Differential scanning calorimetry and wide-angle X-ray studies of these copolymers showed that their properties were determined by the ratio of the lengths of the flexible linear poly(dimethylsiloxane) and rigid poly(1,3-disila-1,3-diphenyl-2-oxaindane)-diphenylsiloxane fragments in the main macromolecular chain. Two-phase systems were obtained with specific flexible and rigid fragment length values in synthesized block copolymers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3462–3467, 2006

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