化学
质子化
铬
乙烯
催化作用
选择性
残留物(化学)
药物化学
烷基化
配体(生物化学)
立体化学
高分子化学
有机化学
离子
生物化学
受体
作者
Yacoob Shaikh,Joanna Gurnham,Khalid Albahily,Sandro Gambarotta,Ilia Korobkov
出处
期刊:Organometallics
[American Chemical Society]
日期:2012-10-25
卷期号:31 (21): 7427-7433
被引量:48
摘要
Chromium complexes of three new ligands, Ph2PN(Me)(CH2)2-X [X = NMe2(PNN); PPh2 (PNP); Py (PNPy)], have been examined vis-à-vis their ability to promote ethylene tetramerization, (PNN)CrCl3(L) [L = THF (1); CH3CN (2)], (PNPy)CrCl3(L) [L = THF (3); CH3CN (4)], and (PNP)CrCl3(THF) (5). In the case of 2 and 4, it was possible to grow crystals suitable for X-ray diffraction. The reaction of 3 with Et3Al afforded the dinuclear [(HN(Me)(CH2)2Py)CrCl2Et]2 (6) containing a trivalent chromium connected to an Et group. During the alkylation though, the ligand has been fragmented with removal of the side arm and protonation of the N atom of the remaining NP residue. All the complexes have been tested for ethylene oligomerization activity. Complex 1 displayed the highest selectivity for 1-octene, upon activation with DMAO in MeCy. Contrary to expectations, complex 6 is not a self-activating catalyst.
科研通智能强力驱动
Strongly Powered by AbleSci AI