An autonomous chemically fuelled small-molecule motor

被引:363
作者
Wilson, Miriam R. [1 ]
Sola, Jordi [1 ,2 ]
Carlone, Armando [1 ,3 ]
Goldup, Stephen M. [1 ,4 ]
Lebrasseur, Nathalie [1 ,5 ]
Leigh, David A. [1 ]
机构
[1] Univ Manchester, Sch Chem, Oxford Rd, Manchester M13 9PL, Lancs, England
[2] Inst Adv Chem Catalonia IQAC CSIC, Jordi Girona 18-26, Barcelona 08034, Spain
[3] Dr Reddys, Chirotech Technol Ctr, Cambridge CB4 0PE, England
[4] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
[5] Queen Mary Univ London, Sch Biol & Chem Sci, London E1 4NS, England
基金
欧洲研究理事会;
关键词
ROTARY MOTOR; DRIVEN; MOTION; CONTRACTION; ROTATION;
D O I
10.1038/nature18013
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular machines are among the most complex of all functional molecules and lie at the heart of nearly every biological process(1). A number of synthetic small-molecule machines have been developed(2), including molecular muscles(3,4), synthesizers(5,6), pumps(7-9), walkers(10), transporters(11) and light-driven(12-16) and electrically(17,18) driven rotary motors. However, although biological molecular motors are powered by chemical gradients or the hydrolysis of adenosine triphosphate (ATP)(1), so far there are no synthetic small-molecule motors that can operate autonomously using chemical energy (that is, the components move with net directionality as long as a chemical fuel is present)(19). Here we describe a system in which a small molecular ring (macrocycle) is continuously transported directionally around a cyclic molecular track when powered by irreversible reactions of a chemical fuel, 9-fluorenylmethoxycarbonyl chloride. Key to the design is that the rate of reaction of this fuel with reactive sites on the cyclic track is faster when the macrocycle is far from the reactive site than when it is near to it. We find that a bulky pyridine-based catalyst promotes carbonate-forming reactions that ratchet the displacement of the macrocycle away from the reactive sites on the track. Under reaction conditions where both attachment and cleavage of the 9-fluorenylmethoxycarbonyl groups occur through different processes, and the cleavage reaction occurs at a rate independent of macrocycle location, net directional rotation of the molecular motor continues for as long as unreacted fuel remains. We anticipate that autonomous chemically fuelled molecular motors will find application as engines in molecular nanotechnology(2,19,20).
引用
收藏
页码:235 / +
页数:7
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