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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.
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页码:2073 / 2078
页数:6
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