Journal
MACROMOLECULES
Volume 37, Issue 14, Pages 5196-5210Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ma049871+
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A simple catalyst of TaBr5, NbBr5, or (NbBr3CH3O)-C-.(CH2)(2)OCH3 is developed, which readily effects polycyclotrimerizations of alpha,omega-alkenediynes {HCequivalent toC(CH2)(m)Cequivalent toCH, m = 4-6 [1(m)]} at room temperature, giving hyperbranched poly(alkenephenylene)s [hb-P1(m)] with high molecular weights (M. up to similar to270 x 10(3)) in high yields (normally >80%). The polymers prepared under optimal reaction conditions are completely soluble in common organic solvents such as toluene, THF, and chloroform. Spectroscopic characterizations prove that the polymers comprise of linear (L) and dendritic units (D) of 1,2,4/1,3,5-trialkylbenzenes and terminal unit (T) of 1,2,4-trialkylbenzene (or 6-alkyltetralin). The L and D units are generated by geostructurally different addition modes, similar to those used by nature to create L and D units of glycogen, a hyperbranched biopolymer. With the aids of model reactions and simulations, detailed structural analyses reveal that hb-P1(4) possesses a degree of branching of 64% and consists of 36%, 32%, and 32% of L, D, and T units, respectively, with 1,2,4-trialkylbenzene being the predominant isomeric structure (74%). The polymer shows outstanding thermal properties: it readily cures when baked at a moderate temperature of 100 degreesC and loses little of its weight when heated to a high temperature of similar to500 degreesC.
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