钯
配体(生物化学)
化学
钳子运动
钳形配体
吡咯
药物化学
二氯甲烷
三乙胺
光化学
高分子化学
催化作用
有机化学
生物化学
受体
溶剂
作者
Aurore Fraix,Martin Lutz,Anthony L. Spek,Robertus J. M. Klein Gebbink,Gerard van Koten,J.-Y. Salaun,Paul-Alain Jaffrès
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2010-01-01
卷期号:39 (11): 2942-2942
被引量:17
摘要
The synthesis of an S,NH,S-pincer ligand possessing a pyrrole core and two O,O-diethylthiophosphonyl groups to design P=S lateral coordination sites is reported. The synthetic procedure to produce this ligand makes use of the nitrogen atom of the pyrrole heterocycle to successively functionalize the ortho-positions with the two O,O-diethylthiophosphonyl moieties. The ortho-functionalization arises from a repetition of a [1,2] base-induced rearrangement allowing the transformation of O,O-diethyl-N-pyrollylthiophosphoramidate to ortho-thiophosphonate. The coordination properties of this tridentate S,NH,S-ligand have been investigated with silver and palladium metals. Reaction of the monoanionic S,N,S-pincer ligand 4 (O,O,O,O-tetraethylpyrrol-2,5-yl-dithiophosphonate) with PdCl(2)(MeCN)(2) at room temperature in the presence of triethylamine gives rise to the formation of the eta(3)-complex [Pd(eta(3)-4')Cl] 5. Ligand 4 also reacts with silver oxide in dichloromethane to produce complex which, in the solid state, exists as a tetramer involving an almost linear arrangement of four silver atoms.
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