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Highly Tactic Cyclic Polynorbornene: Stereoselective Ring Expansion Metathesis Polymerization of Norbornene Catalyzed by a New Tethered Tungsten-Alkylidene Catalyst
The tungsten alkylidyne [ t BuOCO]WC( t Bu) (THF)2 (1) reacts with CO2, leading to complete cleavage of one CO bond, followed by migratory insertion to generate the tungsten-oxo alkylidene 2. Complex 2 is the first catalyst to polymerize norbornene via ring expansion metathesis polymerization to...
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Published in: | Journal of the American Chemical Society 2016-04, Vol.138 (15), p.4996-4999 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The tungsten alkylidyne [ t BuOCO]WC( t Bu) (THF)2 (1) reacts with CO2, leading to complete cleavage of one CO bond, followed by migratory insertion to generate the tungsten-oxo alkylidene 2. Complex 2 is the first catalyst to polymerize norbornene via ring expansion metathesis polymerization to yield highly cis-syndiotactic cyclic polynorbornene. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/jacs.6b00014 |