1-十六炔
外观
1-十六炔 | |
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英文名 | 1-hexadecyne |
识别 | |
CAS号 | 629-74-3 |
PubChem | 12396 |
SMILES |
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InChI |
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InChIKey | UCIDYSLOTJMRAM-UHFFFAOYSA-N |
性质 | |
化学式 | C16H30 |
摩尔质量 | 222.41 g·mol−1 |
熔点 | +15.0 |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
1-十六炔是一种有机化合物,化学式C16H30,可见于北美金縷梅[1]、鱼腥草[2]、羽叶金合欢[3]、辽东栎(Quercus liaotungensis)[4]、牛樟[5]等物种。其可在吸附有氢原子的单晶硅(111)晶面上自发吸附形成一层致密的单分子层[6][7]。
参考资料
[编辑]- ^ Engel R; Gutmann M; Hartisch C; Kolodziej H; Nahrstedt A. Study on the composition of the volatile fraction of Hamamelis virginiana. Planta Medica. 1998-04, 64 (3). doi:10.1055/S-2006-957420.
- ^ Minmin Liang; Meiling Qi; Changbin Zhang; Shan Zhou; Ruonong Fu; Junxiong Huang. Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation. Analytica Chimica Acta. 2005-02, 531 (1). doi:10.1016/J.ACA.2004.09.082.
- ^ 李贵军,汪帆. 臭菜挥发油化学成分的GC-MS分析. 中国调味品. 2014, (6): 118-120. doi:10.3969/j.issn.1000-9973.2014.06.031.
- ^ 周敬林,王斌赫,王国宝. 2种柞树叶片和树皮中的挥发性化学成分鉴定. 蚕业科学. 2017, 43 (3): 459-466. doi:10.13441/j.cnki.cykx.2017.03.015.
- ^ Cheng, Sen-Sung, Chun-Ya Lin, Chih-Kai Yang, Ying-Ju Chen, Min-Jay Chung, ,Shang-Tzen Chan. Chemical Polymorphism and Composition of Leaf Essential Oils of Cinnamomum kanehirae Using Gas Chromatography/Mass Spectrometry, Cluster Analysis, and Principal Component Analysis. Journal of Wood Chemistry and Technology. 2015, 35 (3): 207-219. doi:10.1080/02773813.2014.924967.
- ^ Luc ScheresMarcel GiesbersHan Zuilhof. Self-Assembly of Organic Monolayers onto Hydrogen-Terminated Silicon: 1-Alkynes Are Better Than 1-Alkenes. Langmuir. 2010, 26 (13): 10924–10929. doi:10.1021/la100858q.
- ^ Bart Rijksen,Sidharam P. Pujari,Luc Scheres,; et al. Hexadecadienyl Monolayers on Hydrogen-Terminated Si(111): Faster Monolayer Formation and Improved Surface Coverage Using the Enyne Moiety. Langmuir. 2012, 28 (16): 6577–6588. doi:10.1021/la204770r.
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