Issue 6, 1991

Synthesis and characterisation of pentaphenylcyclo-pentadienyliron arene sandwich complex cations [Fe(η5-C5Ph5)(arene)]+ and the X-ray crystal structure of the [Fe(η5-C5Ph5)(η6-C6H5Me)]+ cation

Abstract

A series of [Fe(η5-C5Ph5)(η6-arene)]+ complex cations [arene = benzene, toluene, o-, m- and p-xylene, mesitylene, durene (1,2,4,5-tetramethylbenzene) or hexamethylbenzene] is reported. The structure of the cation of the toluene derivative was determined by single-crystal X-ray diffraction [refined to R 0.034, R′ 0.038 with 4328 data having I[gt-or-equal] 2.5σ(I)]. It crystallises from acetone as discrete molecules in the monoclinic space group P21/n, with a= 10.016(2), b= 21.568(6), c= 16.920(4)Å, β= 92.17(2)° and Z= 4. The cyclopentadienyl ring binds in an η5 fashion and the Fe–C (C6 ring) bond distances average 2.093(3)Å; the Fe–C (C5 ring) bond distances average 2.113(4)Å. The Fe–C (C5 ring plane) and Fe–C (C6 ring plane) distances are 1.702(5) and 1.588(5)Å, respectively. All complexes exhibit two reversible reductions.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1991, 1499-1505

Synthesis and characterisation of pentaphenylcyclo-pentadienyliron arene sandwich complex cations [Fe(η5-C5Ph5)(arene)]+ and the X-ray crystal structure of the [Fe(η5-C5Ph5)(η6-C6H5Me)]+ cation

L. D. Field, T. W. Hambley, P. A. Lay, C. M. Lindall and A. F. Masters, J. Chem. Soc., Dalton Trans., 1991, 1499 DOI: 10.1039/DT9910001499

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