四丙基硼酸鈉
四丙基硼酸鈉是一種離子型的有機硼化合物,化學式為Na[B(C3H7)4]。它是淺黃白色吸濕性固體。[1]它在水溶液中穩定,但是在空氣中可以自燃;它可以以四氫呋喃溶液的形式儲存數周。[2]
四丙基硼酸鈉 | |
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IUPAC名 Sodium tetrapropylboranuide | |
別名 | 四正丙基硼酸鈉 |
識別 | |
CAS號 | 105146-61-0 |
PubChem | 23676209 |
ChemSpider | 21377657 |
SMILES |
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InChI |
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InChIKey | VKBNWVIDTHWBAZ-UHFFFAOYSA-N |
EINECS | 808-438-1 |
MeSH | C489231 |
性質 | |
化學式 | C12H28BNa |
摩爾質量 | 206.15 g·mol−1 |
相關物質 | |
其他陰離子 | 四苯硼鈉 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
合成
BF
3 · (C
2H
5)
2O + 3 C
3H
7MgBr → B(C
3H
7)
3 + 3 MgBrF + (C
2H
5)
2O
參考文獻
- ^ De Smaele, Tom; Moens, Luc; Dams, Richard; Sandra, Pat; Van Der Eycken, Johan; Vandyck, Jos. Sodium tetra(n-propyl)borate: A novel aqueous in situ derivatization reagent for the simultaneous determination of organomercury, -lead and -tin compounds with capillary gas chromatography–inductively coupled plasma mass spectrometry. Journal of Chromatography A. 1998, 793: 99–106. doi:10.1016/S0021-9673(97)00886-8.
- ^ Schubert, P.; Rosenberg, E.; Grasserbauer, M. Comparison of sodium tetraethylborate and sodium tetra(n-propyl)borate as derivatization reagent for the speciation of organotin and organolead compounds in water samples. Fresenius' Journal of Analytical Chemistry. 2000, 366 (4): 356–360. PMID 11220318. doi:10.1007/s002160050072.
- ^ Honeycutt, Julian B.; Riddle, James M. Preparation and Reactions of Sodium Tetraethylboron and Related Compounds1. Journal of the American Chemical Society. 1961, 83 (2): 369–373. doi:10.1021/ja01463a027.