Departments of Chemistry, Physics, Chemical Engineering, and Geosciences, Virginia Tech, Blacksburg, Virginia 24061, United States.
Département de Physique, Université de Montréal, Complexe des Sciences, 1375 Avenue Thérèse-Lavoie-Roux, Montréal, QC H2 V 0B3, Canada.
J Am Chem Soc. 2022 Sep 14;144(36):16287-16291. doi: 10.1021/jacs.2c06951. Epub 2022 Aug 29.
We report the first experimental characterization of isomerically pure and pristine C fullertubes, [5,5] C-D(1) and [10,0] C-D(10766). These new molecules represent the highest aspect ratio fullertubes isolated to date; for example, the prior largest empty cage fullertube was [5,5] C-D(1). This increase of 20 carbon atoms represents a gigantic leap in comparison to of C-C fullerene research. Moreover, the [10,0] C-D(10766) fullertube has an end-cap derived from C-I and is a new fullertube whose C end-cap has not yet been isolated experimentally. Theoretical and experimental analyses of anisotropic polarizability and UV-vis assign C isomer I as a [5,5] C-D(1) fullertube. C isomer II matches a [10,0] C-D(10766) fullertube. These structural assignments are further supported by Raman data showing metallic character for [5,5] C-D(1) and nonmetallic character for C-D(10766). STM imaging reveals a tubular structure with an aspect ratio consistent with a [5,5] C-D(1) fullertube. With microgram quantities not amenable to crystallography, we demonstrate that DFT anisotropic polarizability, augmented by long-accepted experimental analyses (HPLC retention time, UV-vis, Raman, and STM) can be synergistically used (with DFT) to down select, predict, and assign C fullertube candidate structures. From 10 774 mathematically possible IPR C structures, this anisotropic polarizability paradigm is quite favorable to distinguish tubular structures from carbon soot. Identification of isomers I and II was surprisingly facile, i.e., two purified isomers for two possible structures of widely distinguishing features. These metallic and nonmetallic C fullertube isomers open the door to both fundamental research and application development.
我们报告了首次对同手性纯的、原始的 C 富勒管 [5,5] C-D(1) 和 [10,0] C-D(10766) 的实验特性进行了描述。这些新分子代表了迄今为止分离出的具有最高纵横比的富勒管;例如,之前最大的空笼富勒管是 [5,5] C-D(1)。与 C-C 富勒烯研究相比,这增加了 20 个碳原子,是一个巨大的飞跃。此外,[10,0] C-D(10766)富勒管的端帽来源于 C-I,是一种新的富勒管,其 C 端帽尚未在实验中分离出来。各向异性极化率的理论和实验分析以及 UV-vis 分配表明,C 异构体 I 是 [5,5] C-D(1) 富勒管。C 异构体 II 与 [10,0] C-D(10766) 富勒管匹配。拉曼数据进一步支持这些结构分配,表明 [5,5] C-D(1) 具有金属特性,而 C-D(10766) 具有非金属特性。STM 成像显示出具有与 [5,5] C-D(1) 富勒管一致的纵横比的管状结构。由于微克量级不适合结晶学,我们证明了 DFT 各向异性极化率,加上长期接受的实验分析(HPLC 保留时间、UV-vis、拉曼和 STM)可以协同使用(与 DFT 一起)对 C 富勒管候选结构进行向下选择、预测和分配。从 10774 个数学上可能的 IPR C 结构中,这种各向异性极化率范例非常有利于将管状结构与碳烟区分开来。异构体 I 和 II 的鉴定非常简单,即两种可能结构的两种纯化异构体具有广泛区分的特征。这些金属和非金属 C 富勒管异构体为基础研究和应用开发打开了大门。