Hydrosilylation reactions of bis(dimethylsilyl)acetylenes: A potential route to novel σ- and π-conjugated polymers

Tetrahedron Letters

Volumn 37, Issue 10, 1996, Pages 1579-1582

  Son, David Y ^a,b   Bucca, Daniel ^a   Keller, Teddy M ^a  

^a NAVAL RESEARCH LABORATORY   (United States)

^b SOUTHERN METHODIST UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; POLYMERIZATION; TECHNIQUE;

EID: 0029936441     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00095-0     Document Type: Article

References (20)

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3. (a) Ijadi-Maghsoodi, S.; Pang, Y.; Barton, T. J. J. Polym. Sci., Part A: Polym. Chem. 1990, 28, 955.
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16. 3), 113.2 (C≡C), 125.2, 126.6, 128.3, 128.5, 137.9, 145.7.
17. 13C NMR (ppm) -1.23 (-SiC), 113.1 (C≡C), complex set of peaks between 122 and 144 ppm.
18. 13C NMR (ppm) -1.21 (-SiC), 113.2 (C≡C), 122.2, 126.2, 128.1, 131.6, 136.8, 144.3.
19. 13C NMR (ppm) -1.10, 78.0, 83.6, 113.0, 125.5, 126.5, 126.9, 132.3, 137.9, 145.2.
20. 13C NMR (ppm) -1.10, 77.3, 84.0, 113.2, complex set of peaks between 125 and 145 ppm.