Moreno-Vicente Antonio, Abella Laura, Azmani Khalid, Rodríguez-Fortea Antonio, Poblet Josep M
Departament de Química Física i Inorgànica, Universitat Rovira i Virgili , c/Marcel·lí Domingo 1, 43007 Tarragona, Spain.
J Phys Chem A. 2018 Mar 1;122(8):2288-2296. doi: 10.1021/acs.jpca.7b12228. Epub 2018 Feb 20.
Halogenation has been one of the most used strategies to explore the reactivity of empty carbon cages. In particular, the higher reactivity of non-IPR fullerenes, i.e., those fullerenes that do not satisfy the isolated pentagon rule (IPR), has been used to functionalize and capture these less stable fullerenes. Here, we have explored the stability of the non-IPR isomer C(11188) with C symmetry, which is topologically linked to the only IPR isomer of C, as well as its reactivity to chlorination. DFT calculations and Car-Parrinello molecular dynamics simulations suggest that chlorination takes places initially in nonspecific sites, once carbon cages are formed. When the temperature in the arc reactor decreases sufficiently, Cl atoms are trapped on the fullerene surface, migrating from not-so-favored positions to reach the most favored sites in the pentalene. We have also discussed why cage C-C(11188) is found to take four chlorines, whereas cage C-C(14049) is observed to capture 10 of them, even though these two fullerenes are closely related by a simple C insertion.
卤化一直是探索空碳笼反应活性最常用的策略之一。特别是,非IPR富勒烯(即那些不满足孤立五边形规则(IPR)的富勒烯)具有更高的反应活性,已被用于官能化和捕获这些不太稳定的富勒烯。在此,我们研究了具有C对称性的非IPR异构体C(11188)的稳定性,它与C的唯一IPR异构体拓扑相连,以及它对氯化的反应活性。密度泛函理论计算和Car-Parrinello分子动力学模拟表明,一旦碳笼形成,氯化最初发生在非特定位置。当电弧反应器中的温度充分降低时,Cl原子被困在富勒烯表面,从不太有利的位置迁移到并五苯中最有利的位置。我们还讨论了为什么发现笼状C-C(11188)能容纳四个氯原子,而笼状C-C(14049)能捕获其中的十个氯原子,尽管这两个富勒烯通过简单插入一个C原子而密切相关。