Cobalt-Mediated Radical Coupling (CMRC): An Unusual Route to Midchain-Functionalized Symmetrical Macromolecules

被引:47
作者
Debuigne, Antoine [1 ]
Poli, Rinaldo [2 ,3 ]
De Winter, Julien [4 ]
Laurent, Pascal [5 ]
Gerbaux, Pascal [4 ]
Dubois, Philippe [6 ]
Wathelet, Jean-Paul [5 ]
Jerome, Christine [1 ]
Detrembleur, Christophe [1 ]
机构
[1] Univ Liege, Ctr Educ & Res Macromol, B-4000 Liege, Belgium
[2] Univ Toulouse, UPS, INPT, Chim Coordinat Lab, F-31077 Toulouse, France
[3] Inst Univ France, F-75005 Paris, France
[4] Univ Mons, Mass Spectrometry Ctr, Organ Chem Lab, B-7000 Mons, Belgium
[5] Gembloux Agr Univ, FUSAGx, Unit Gen & Organ Chem, B-5030 Gembloux, Belgium
[6] Univ Mons, CIRMAP, Lab Polymer & Composite Mat, B-7000 Mons, Belgium
关键词
cobalt; dienes; poly-(acrylonitrile)s; polymerization; radical reactions; VINYL-ACETATE; TRANSFER POLYMERIZATION; POLY(METHYL ACRYLATE); DISPERSED SYSTEMS; BLOCK-COPOLYMERS; MOLECULAR-WEIGHT; POLYSTYRENE; MICROSTRUCTURE; ACRYLONITRILE; POLYBUTADIENE;
D O I
10.1002/chem.200902618
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cobalt-mediated radical coupling (CMRC) is a straightforward approach to the synthesis of symmetrical macromolecules that relies on the addition of 1,3-diene compounds onto polymer precursors preformed by cobalt-mediated radical polymerization (CMRP). Mechanistic features that make this process so efficient for radical polymer coupling are reported here. The mechanism was established on the basis of NMR spectroscopy and MALDI-MS analyses of the coupling product and corroborated by DFT calculations. A key feature of CMRC is the preferential insertion of two diene units in the middle of the chain of the coupling product mainly according to it trans-1,4-addition pathway. The large tolerance of CMRC towards the diene Structure is demonstrated and the impact of this new Coupling method on macromolecular engineering is discussed, especially for midchain functionalization of polymers. It is worth noting that the interest in CMRC goes beyond the field of polymer chemistry. since it constitutes a novel carbon-carbon bond formation method that could be applied to small organic molecules.
引用
收藏
页码:1799 / 1811
页数:13
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