Synthesis and crystal structures of novel group 6B metal carbonyl complexes with N‐(4‐methyl‐2‐ pyridinyl)‐P,P‐diphenylphosphinous amide ligand

Harbi Tomah AL-Masri, Suzan Mohammed Alrawashdeh, Akram Ali Almejled, Ziad moussa
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Abstract

The reaction of N‐(4‐methyl‐2‐pyridinyl)‐P,P‐diphenylphosphinous amide ligand 4‐Me‐C5H3N‐2‐NH(PPh2) (1) with M(CO)6 (M = Cr, Mo, W) in refluxing toluene afforded a mononuclear group 6B metal tetracarbonyls [M(CO)4{1‐κ2P,N}] (M = Cr(2), Mo(3), W(4) ). Complexes 2–4 were characterized by multinuclear NMR (1H, 13C and 31P NMR) and IR spectroscopy, and their structures were also determined by single crystal X‐ray diffraction. 2 and 4 represent the first examples of structurally characterized complexes of such ligands with group 6B metal carbonyls.
新型 6B 族金属羰基配合物与 N-(4-甲基-2-吡啶基)-P,P-二苯基膦酰胺配体的合成及晶体结构
在回流甲苯中,N-(4-甲基-2-吡啶基)-P,P-二苯基膦酰胺配体 4-Me-C5H3N-2-NH(PPh2) (1) 与 M(CO)6(M = Cr、Mo、W)反应,得到单核 6B 族金属四碳化物 [M(CO)4{1-κ2P,N}] (M = Cr(2)、Mo(3)、W(4) )。通过多核核磁共振(1H、13C 和 31P NMR)和红外光谱对 2-4 号络合物进行了表征,并通过单晶 X 射线衍射确定了它们的结构。2 和 4 是此类配体与 6B 族金属羰基形成的具有结构特征的络合物的首例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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