Solid-State Pathway Control via Reaction-Directing Heteroatoms: Ordered Pyridazine Nanothreads through Selective Cycloaddition

被引:30
作者
Dunning, Samuel G. [1 ]
Zhu, Li [1 ]
Chen, Bo [2 ,3 ]
Chariton, Stella [4 ]
Prakapenka, Vitali B. [4 ]
Somayazulu, Maddury [5 ]
Strobel, Timothy A. [1 ]
机构
[1] Carnegie Inst Sci, Earth & Planets Lab, Washington, DC 20015 USA
[2] Donostia Int Phys Ctr, Donostia San Sebastian 20018, Spain
[3] IKERBASQUE Basque Fdn Sci, Bilbao 48009, Spain
[4] Univ Chicago, Ctr Adv Radiat Sources, Chicago, IL 60637 USA
[5] Argonne Natl Lab, Xray Sci Div, HPCAT, Lemont, IL 60439 USA
关键词
PRESSURE-INDUCED POLYMERIZATION; MECHANICAL-PROPERTIES; CARBON NITRIDE; THERMAL-DECOMPOSITION; NITROGEN; BENZENE; 1ST-PRINCIPLES; DYNAMICS; PATTERNS; PYRIDINE;
D O I
10.1021/jacs.1c12143
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanothreads are one-dimensional nanomaterials composed of a primarily sp(3) hydrocarbon backbone, typically formed through the compression of small molecules to high pressures. Although nanothreads have been synthesized from a range of precursors, controlling reaction pathways to produce atomically precise materials remains a difficult challenge. Here, we show how heteroatoms within precursors can serve as "thread-directing" groups by selecting for specific cycloaddition reaction pathways. By using a less-reactive diazine group within a six-membered aromatic ring, we successfully predict and synthesize the first carbon nanothread material derived from pyridazine (1,2-diazine, C4H4N2). Compared with previous nanothreads, the synthesized polypyridazine, shows a predominantly uniform chemical structure with exceptional long-range order, allowing for structural characterization using vibrational spectroscopy and X-ray diffraction. The results demonstrate how thread-directing groups can be used for reaction pathway control and the formation of chemically precise nanothreads with a high degree of structural order.
引用
收藏
页码:2073 / 2078
页数:6
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