Synthesis and characterization of perhalogenated triphenylphosphine-cymantrenes [(C5X5)Mn(CO)2(PPh3)] (X = F, Cl, Br) and [(C5HI4)Mn(CO)2(PPh3)]

被引：12

作者：

Klein-Hessling, Christian ^{[1
]}

Blockhaus, Tobias ^{[1
]}

Suenkel, Karlheinz ^{[1
]}

机构：

[1] Ludwig Maximilians Univ Munchen, Butenandtstr 9, D-81377 Munich, Germany

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2021年 / 943卷

关键词：

Cymantrene; Photolysis; Perhalocyclopentadienyl complexes; METAL-CARBONYL-COMPLEXES; COORDINATION CHEMISTRY; HALOGEN-DERIVATIVES; CRYSTAL-STRUCTURE; CYCLOPENTADIENES; ALKYNES; MANGANESE; REACTIVITY; EXCHANGE; LIGAND;

D O I：

10.1016/j.jorganchem.2021.121833

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Photolysis of the monohalocymantrenes [(C5H4X)Mn(CO)(3)] (X = F, Cl, Br, I) in the presence of triphenylphosphine yields the corresponding dicarbonyl complexes [(C5H4X)Mn(CO)(2)(PPh3)]. Stepwise metalation and electrophilic quench with (PhSO2)(2)NF, C2Cl6, C2HBr5 or I-2, respectively leads to [(C5H2F3)Mn(CO)(2)(PPh3)], [(C5X5)Mn(CO)(2)(PPh3)] (X=Cl, Br) and [(C5HI4)Mn(CO)(2)(PPh3)]. Further fluorination or iodination leads only to decomposition. However, lithiation of [(C5H2F3)Mn(CO)(2)(PPh3)] is possible and electrophilic quench with C2Cl6 leads finally to [(C5F3Cl2)Mn(CO)(2)(PPh3)]. The crystal structures of the tetra- and pentasubstituted compounds are reported. (C) 2021 Elsevier B.V. All rights reserved.

引用

页数：12

共 50 条

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