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通过顺序[1,2]磷酰基-Fries 重排构建具有吡咯核的单核阴离子 S,N,S-三齿配体。钯和银配位配合物的表征。

Construction of a monoanionic S,N,S-pincer ligand with a pyrrole core by sequential [1,2] phospho-Fries rearrangement. Characterization of palladium and silver coordination complexes.

机构信息

Université Européenne de Bretagne, Université de Brest, CNRS UMR 6521, CEMCA, IFR 148 ScInBios, 6 Avenue Le Gorgeu, 29238, Brest, France.

出版信息

Dalton Trans. 2010 Mar 21;39(11):2942-6. doi: 10.1039/b923351b. Epub 2010 Feb 5.

Abstract

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.

摘要

报道了一种具有吡咯核和两个 O,O-二乙基硫膦酰基的 S,NH,S-三齿配体的合成,旨在设计 P=S 侧配位位点。该配体的合成过程利用吡咯杂环的氮原子,依次在邻位与两个 O,O-二乙基硫膦酰基官能化。邻位官能化源于[1,2]碱基诱导重排的重复,允许 O,O-二乙基-N-吡咯基硫代磷酰胺转化为邻位硫代膦酸酯。该三齿 S,NH,S-配体的配位性质已用银和钯金属进行了研究。在室温下,将单阴离子 S,N,S-三齿配体 4(O,O,O,O-四乙基吡咯-2,5-二硫代膦酸酯)与 PdCl(2)(MeCN)(2)在三乙胺存在下反应,生成 eta(3)-配合物[Pd(eta(3)-4')Cl]5。配体 4 还与氧化银在二氯甲烷中反应生成复合物,在固态中,复合物以涉及四个银原子几乎线性排列的四聚体形式存在。

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