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環[18]碳

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维基百科,自由的百科全书
(重定向自环碳
环[18]碳
识别
CAS号 126487-09-0  checkY
PubChem 14940714
ChemSpider 74015635
SMILES
 
  • C1#CC#CC#CC#CC#CC#CC#CC#CC#C1
性质
化学式 C18
摩尔质量 216.19 g·mol⁻¹
密度 1.38±0.1 g·cm−3(20 °C)[1]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

环[18]碳环十八-1,3,5,7,9,11,13,15,17-九炔碳的同素異形體之一,化学式C
18
,几乎不溶于水。[1]它是一种环碳多炔,由十八个碳原子以单叁键交替构成环。环[18]碳是预测能够热力学稳定最小的环[n]碳,理论应变能为72 kcal/mol。[2][3]

历史和制备

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早在1991年,便有人对环[18]碳的结构进行预测,并进行过有关计算,[4]但其合成却在2019年才被IBM牛津大学的联合团队[5]通过环丁酮结构的数个位点进行电化学脱羰基反应制得:[6]

环碳的合成
环碳的合成

它也可由C18Br6的脱溴反应制得。[7]

性质

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IBM研究人员发现,环[18]碳的电子结构英语electronic structure由交替的单叁键构成,而非累计双键结构,它在理论上是一种半导体[6]

在该化合物中,C—C键的键长为1.36 Å,C≡C的键长为1.20 Å。[5]

参考文献

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  1. ^ 1.0 1.1 Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-8-21]
  2. ^ George A. Adamson; Charles W. Rees. Towards the total synthesis of cyclo[n]carbons and the generation of cyclo[6]carbon. J. Chem. Soc., Perkin Trans. 1. 1996, (13): 1535–1543. doi:10.1039/P19960001535. 
  3. ^ François Diederich; Yves Rubin; Carolyn B. Knobler; Robert L. Whetten; Kenneth E. Schriver; Kendall N. Houk; Yi Li. All-Carbon Molecules: Evidence for the Generation of Cyclo[18]carbon from a Stable Organic Precursor. Science. 1989-09-08, 245 (4922): 1088–1090. Bibcode:1989Sci...245.1088D. PMID 17838807. doi:10.1126/science.245.4922.1088. 
  4. ^ Parasuk, Vudhichai; Almlof, Jan; Feyereisen, Martin W. The [18] all-carbon molecule: cumulene or polyacetylene?. Journal of the American Chemical Society. 1991, 113 (3): 1049–1050. ISSN 0002-7863. doi:10.1021/ja00003a052. 
  5. ^ 5.0 5.1 Kaiser, Katharina; Scriven, Lorel M.; Schulz, Fabian; Gawel, Przemyslaw; Gross, Leo; Anderson, Harry L. An sp-hybridized molecular carbon allotrope, cyclo[18]carbon. Science. 2019-08-15 [2019-08-21]. doi:10.1126/science.aay1914. (原始内容存档于2019-08-21). 
  6. ^ 6.0 6.1 Castelvecchi, Davide. Chemists make first-ever ring of pure carbon. Nature. 2019-08-15 [2019-08-16]. doi:10.1038/d41586-019-02473-z. (原始内容存档于2019-08-16) (英语). 
  7. ^ Lorel M. Scriven, Katharina Kaiser, Fabian Schulz, Alistair J. Sterling, Steffen L. Woltering, Przemyslaw Gawel, Kirsten E. Christensen, Harry L. Anderson, Leo Gross. Synthesis of Cyclo[18]carbon via Debromination of C 18 Br 6. Journal of the American Chemical Society. 2020-07-29, 142 (30): 12921–12924 [2020-08-22]. ISSN 0002-7863. doi:10.1021/jacs.0c05033. (原始内容存档于2020-10-17) (英语). 

拓展阅读

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  • Sen, Sabyasachi; Seal, Prasenjit; Chakrabarti, Swapan. Explicit role of dynamical and nondynamical electron correlations on broken symmetry inC4N+2clusters. Physical Review B. 2006, 73 (24). ISSN 1098-0121. doi:10.1103/PhysRevB.73.245401. 
  • Feyereisen, Martin; Gutowski, Maciej; Simons, Jack; Almlöf, Jan. Relative stabilities of fullerene, cumulene, and polyacetylene structures for Cn:n=18–60. The Journal of Chemical Physics. 1992, 96 (4): 2926–2932. ISSN 0021-9606. doi:10.1063/1.461989. 
  • Murphy, Veronica L.; Farfan, Camille; Kahr, Bart. Chiroptical structure-property relations in cyclo[18]carbon and its in silico hydrogenation products. Chirality. 2018, 30 (4): 325–331. ISSN 0899-0042. doi:10.1002/chir.22817.