Mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I by AgBF4

Bruce M. Mattson; William A.G. Graham

doi:10.1021/ic50224a012

Mechanism of halide abstraction from (η⁵-C₅H₅)Fe(CO)₂I by AgBF₄

Bruce M. Mattson, William A.G. Graham

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Abstract

The mechanism of halide abstraction from (η⁵-C₅H₅)Fe(CO)₂I with AgBF₄ was investigated by ¹H NMR (CDCl₃ solvent) and infrared (CH₂Cl₂ and CHCl₃ solvents) spectroscopic methods. (η⁵-C₅H₅)Fe(CO)₂I initially forms a silver(I) adduct formulated as (η⁵-C₅H₅)Fe(CO)₂IAg⁺, which decomposes to yield AgI and, in the presence of excess (η⁵-C₅H₅)Fe(CO)₂I, the iodine-bridged species [(η⁵-C₅H₅)Fe(CO)₂] ₂IBF₄. This material then reacts with a second 0.5 equiv of AgBF₄ to yield (η⁵-C₅H₅)Fe(CO)₂BF₄, in which tetrafluoroborate is coordinated.

Original language	English (US)
Pages (from-to)	3186-3189
Number of pages	4
Journal	Inorganic Chemistry
Volume	20
Issue number	10
DOIs	https://doi.org/10.1021/ic50224a012
State	Published - Jan 1 1981
Externally published	Yes

All Science Journal Classification (ASJC) codes

Physical and Theoretical Chemistry
Inorganic Chemistry

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title = "Mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I by AgBF4",

abstract = "The mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I with AgBF4 was investigated by 1H NMR (CDCl3 solvent) and infrared (CH2Cl2 and CHCl3 solvents) spectroscopic methods. (η5-C5H5)Fe(CO)2I initially forms a silver(I) adduct formulated as (η5-C5H5)Fe(CO)2IAg+, which decomposes to yield AgI and, in the presence of excess (η5-C5H5)Fe(CO)2I, the iodine-bridged species [(η5-C5H5)Fe(CO)2] 2IBF4. This material then reacts with a second 0.5 equiv of AgBF4 to yield (η5-C5H5)Fe(CO)2BF4, in which tetrafluoroborate is coordinated.",

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year = "1981",

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doi = "10.1021/ic50224a012",

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journal = "Inorganic Chemistry",

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T1 - Mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I by AgBF4

AU - Mattson, Bruce M.

AU - Graham, William A.G.

PY - 1981/1/1

Y1 - 1981/1/1

N2 - The mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I with AgBF4 was investigated by 1H NMR (CDCl3 solvent) and infrared (CH2Cl2 and CHCl3 solvents) spectroscopic methods. (η5-C5H5)Fe(CO)2I initially forms a silver(I) adduct formulated as (η5-C5H5)Fe(CO)2IAg+, which decomposes to yield AgI and, in the presence of excess (η5-C5H5)Fe(CO)2I, the iodine-bridged species [(η5-C5H5)Fe(CO)2] 2IBF4. This material then reacts with a second 0.5 equiv of AgBF4 to yield (η5-C5H5)Fe(CO)2BF4, in which tetrafluoroborate is coordinated.

AB - The mechanism of halide abstraction from (η5-C5H5)Fe(CO)2I with AgBF4 was investigated by 1H NMR (CDCl3 solvent) and infrared (CH2Cl2 and CHCl3 solvents) spectroscopic methods. (η5-C5H5)Fe(CO)2I initially forms a silver(I) adduct formulated as (η5-C5H5)Fe(CO)2IAg+, which decomposes to yield AgI and, in the presence of excess (η5-C5H5)Fe(CO)2I, the iodine-bridged species [(η5-C5H5)Fe(CO)2] 2IBF4. This material then reacts with a second 0.5 equiv of AgBF4 to yield (η5-C5H5)Fe(CO)2BF4, in which tetrafluoroborate is coordinated.

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Mechanism of halide abstraction from (η⁵-C₅H₅)Fe(CO)₂I by AgBF₄

Abstract

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