Chain stopper engineering for hydrogen bonded supramolecular polymers

被引:15
|
作者
Pinault, Thomas [1 ,2 ]
Andrioletti, Bruno [3 ]
Bouteiller, Laurent [1 ,2 ]
机构
[1] Univ Paris 06, UPMC, UMR 7610, F-75005 Paris, France
[2] CNRS, UMR 7610, F-75005 Paris, France
[3] Univ Lyon 1, ICBMS, UMR 5246, F-69622 Villeurbanne, France
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2010年 / 6卷
关键词
chain stopper; gel; hydrogen bond; supramolecular polymer; urea; UREA; VISCOELASTICITY; ORGANOGELS; DYNAMICS; GELATORS; GELS;
D O I
10.3762/bjoc.6.102
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Supramolecular polymers are linear chains of low molar mass monomers held together by reversible and directional non-covalent interactions, which can form gels or highly viscous solutions if the self-assembled chains are sufficiently long and rigid. The viscosity of these solutions can be controlled by adding monofunctional compounds, which interact with the chain extremities: chain stoppers. We have synthesized new substituted ureas and thioureas and tested them as chain stoppers for a bis-urea based supramolecular polymer. In particular, the bis-thiourea analogue of the bis-urea monomer is shown not to form a supramolecular polymer, but a good chain stopper, because it is a strong hydrogen bond donor and a weak acceptor. Moreover, all substituted ureas tested reduce the viscosity of the supramolecular polymer solutions, but the best chain stopper is obtained when two hydrogen bond acceptors are placed in the same relative position as for the monomer and when no hydrogen bond donor is present.
引用
收藏
页码:869 / 875
页数:7
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