Abstract
Polysiloxanes with pendant poly(ethylene oxide) side chains (4 were prepared by the dehydrocoupling reaction of poly(methylhydrosiloxane) (PMHS, 3 with 2-(2-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)ethoxy)ethanol (1 and poly(ethylene glycol) methyl ether (2 using a metal catalyst. Catalysts investigated were tin(II) 2-ethylhexanoate, Rh(Ph3P)3Cl, and Pd2(dba)3. The reaction of a cyclic siloxane, D4 H, with 1 catalyzed by Pd2(dba)3 was also carried out to synthesize siloxane 6. The polysiloxanes were characterized by 1H NMR, 29Si NMR, FT-IR, and GPC. 29Si NMR study of these comb-like polysiloxanes revealed that there is a significant difference in the structure of the siloxane polymers prepared depending upon the catalyst. M, D, and T units were observed when tin(II) was used as a catalyst, but only M and D units were detected when Rh(Ph3P)3Cl or Pd2(dba)3 was employed. Furthermore, M and T units are negligible for the cyclic siloxane 3 using Pd2(dba)3. A mechanism is proposed to account for these observations.
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Zhang, R., Zhang, Z., Amine, K. et al. Modification of polymethylhydrosiloxane by dehydrocoupling reactions catalyzed by transition metal complexes: Evidence for the preservation of linear siloxane structures. Silicon Chem 2, 271–277 (2005). https://doi.org/10.1007/s11201-005-4059-6
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DOI: https://doi.org/10.1007/s11201-005-4059-6