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Restricting shuttling in bis(imidazolium)•••pillar[5]arene rotaxanes using metal coordination
被引:21
|作者:
Langer, Philipp
[1
]
Yang, Lixu
[1
]
Pfeiffer, Constance R.
[1
]
Lewis, William
[1
]
Champness, Neil R.
[1
]
机构:
[1] Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, England
基金:
英国工程与自然科学研究理事会;
关键词:
HETEROCYCLIC CARBENE COMPLEXES;
DEGENERATE MOLECULAR SHUTTLES;
HOST-GUEST COMPLEXATION;
EFFECTIVE BINDING;
AXLE LENGTH;
WATER;
RECOGNITION;
DISCRIMINATION;
FERROCENIUM;
MECHANISM;
D O I:
10.1039/c8dt04096f
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Metal coordination to a series of bis (imidazolium)center dot center dot center dot pillar[5] arene [2]rotaxanes through the formation of metal-carbene bonds facilitates a new strategy to restrict the shuttling motion in [2] rotaxanes. Whereas the pillar[5] arene macrocycle rapidly shuttles along the full length of the bis (imidazolium) rod for the parent [2]rotaxane, Ag(I) coordination to the imidazolium groups through the formation of N-heterocyclic carbenes leads to restricted motion, effectively confining the shuttling motion of the [2] rotaxane. The Ag(I) coordinated [2] rotaxanes can be reacted further, either removing the Ag-carbene species to recreate the parent [2] rotaxane, or reaction with more bulky Pd(II) species to further restrict the shuttling motion through steric inhibition.
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页码:58 / 64
页数:7
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