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When Attempting Chain Extension, Even Without Solvent, It Is Not Possible to Avoid Chojnowski Metathesis Giving D

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Jan 20
PMID 33466286
Citations 3
Authors
Affiliations
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Abstract

A simple, mild and efficient method to prepare HSi- or HOSi-telechelic, high-molecular-weight polydimethylsiloxane polymers (to 41,600 g·mol) using the one-shot hydrolysis of MM is reported; titration of the water allowed for higher molecular weights (to 153,900 g·mol). The "living" character of the chain extension processes was demonstrated by adding a small portion of MM and B(CF) (BCF) to a first formed polymer, which led to a ~2-fold, second growth in molecular weight. The heterogeneous reaction reached completion in less than 30 min, much less in some cases, regardless of whether it was performed neat or 50 wt% in dry toluene; homogeneous reactions in toluene were much slower. The process does not involve traditional redistribution, as judged by the low quantities (<3%) of D produced. However, it is not possible to avoid Chojnowski metathesis from MDDM giving D, which occurs competitively with chain extension.

Citing Articles

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References
1.
Franzen A, Greene T, Van Landingham C, Gentry R . Toxicology of octamethylcyclotetrasiloxane (D). Toxicol Lett. 2017; 279 Suppl 1:2-22. DOI: 10.1016/j.toxlet.2017.06.007. View

2.
Wang D, Steer H, Tait T, Williams Z, Pacepavicius G, Young T . Concentrations of cyclic volatile methylsiloxanes in biosolid amended soil, influent, effluent, receiving water, and sediment of wastewater treatment plants in Canada. Chemosphere. 2012; 93(5):766-73. DOI: 10.1016/j.chemosphere.2012.10.047. View

3.
Brook M . New Control Over Silicone Synthesis using SiH Chemistry: The Piers-Rubinsztajn Reaction. Chemistry. 2018; 24(34):8458-8469. DOI: 10.1002/chem.201800123. View

4.
Schneider A, Chen Y, Brook M . Trace water affects tris(pentafluorophenyl)borane catalytic activity in the Piers-Rubinsztajn reaction. Dalton Trans. 2019; 48(36):13599-13606. DOI: 10.1039/c9dt02756d. View

5.
Fuchise K, Igarashi M, Sato K, Shimada S . Organocatalytic controlled/living ring-opening polymerization of cyclotrisiloxanes initiated by water with strong organic base catalysts. Chem Sci. 2018; 9(11):2879-2891. PMC: 5914541. DOI: 10.1039/c7sc04234e. View