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铁(II)模板合成苯并环三膦和三胂大环。

Iron(II) template synthesis of benzannulated triphospha- and triarsamacrocycles.

机构信息

School of Chemistry, Cardiff University, Cardiff, UK CF10 3AT.

出版信息

Dalton Trans. 2011 Oct 7;40(37):9525-32. doi: 10.1039/c0dt01724h. Epub 2011 Aug 19.

DOI:10.1039/c0dt01724h
PMID:21853170
Abstract

Nine-membered 1,4,7-triphospha- and triarsamacrocycles with unsaturated benzo-backbones have been prepared using the Cp(R)Fe unit as a template. The cyclisation involves the attack of a coordinated phosphide (or arsenide) nucleophile at an activated, electrophilic ortho-fluorophenyl substituent on a neighbouring pnictide donor. The macrocycle assembly is of the 2 + 1 type where two new chelate rings are formed from appropriately derivatised bidentate and monodentate phosphines/arsines. Both (η(5)-C(5)H(5))Fe and (η(5)-C(5)Me(5))Fe may be employed for the cyclisation with higher yields generally being observed with the unsubstituted Cp. All new compounds have been characterised by spectroscopic and analytical methods including the single-crystal X-ray structure determination of (η(5)-C(5)H(5))Fe(tribenzo-9aneP(3)-Ph,Ph(F)(2)), 3a, and (η(5)-C(5)H(5))Fe(tribenzo-9aneAs(3)-Ph,Ph(F)(2)), 5, as the tetraphenylborate salts. The crystal structures are isomorphous and show the unique conformation of these new macrocycles with a 'cup shaped' cavity formed by the rigid benzo-backbones. The 9aneAs(3) derivative is the first example of a nine-membered triarsamacrocycle.

摘要

具有不饱和苯并骨架的九元 1,4,7-三膦和三胂大环已使用 Cp(R)Fe 单元作为模板制备。环化涉及配位的磷化物(或胂化物)亲核试剂在相邻的磷供体的活化、亲电邻氟苯基取代基上的进攻。大环组装为 2 + 1 型,其中两个新的螯合环由适当衍生的双齿和单齿膦/胂形成。(η(5)-C(5)H(5))Fe 和 (η(5)-C(5)Me(5))Fe 都可用于环化,通常未取代的 Cp 产生更高的产率。所有新化合物均通过光谱和分析方法进行了表征,包括 (η(5)-C(5)H(5))Fe(tribenzo-9aneP(3)-Ph,Ph(F)(2)),3a 和 (η(5)-C(5)H(5))Fe(tribenzo-9aneAs(3)-Ph,Ph(F)(2)),5 的单晶 X 射线结构测定,它们是四苯硼酸盐盐。晶体结构是同构的,显示了这些新大环的独特构象,刚性苯并骨架形成了“杯形”空腔。9aneAs(3) 衍生物是第一个九元三胂大环的例子。

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