2000
DOI: 10.1021/om000462l
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Reaction of [(1-H-Hydronaphthalene)Mn(CO)3] with Pyridine in the Presence of Halogenated Solvent:  The Role of Ring-Slippage in [(1-H-Hydronaphthalene)Mn(CO)3]

Abstract: Halogenated solvents such as dichloromethane, dibromomethane, bromochloromethane, chloroform, and carbon tetrachloride react with [(1-H-hydronaphthaelene)Mn(CO)3] (1) and pyridines (py‘) to give the halogeno complex [Mn(CO)3(py‘)2X] (X = Cl, Br) and naphthalene. The C−H and C−X cleavage reactions are dependent upon the electronic and steric properties of the pyridine. The structure of fac-[Mn(CO)3(4-Me-py)2Cl] (5b) has been established by X-ray diffraction study.

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Cited by 6 publications
(1 citation statement)
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“…Recently, we studied the chemistry of [(1 H -hydronaphthalene)Mn(CO) 3 ] and attempted to synthesize the iron analogue [(1 H -hydronaphthalene)Fe(CO) 3 ] + via the reaction of 1,2-dihydronaphthalene with Fe 2 (CO) 9 followed by a hydride abstraction by trityl cation. However, this procedure was unsuccessful.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, we studied the chemistry of [(1 H -hydronaphthalene)Mn(CO) 3 ] and attempted to synthesize the iron analogue [(1 H -hydronaphthalene)Fe(CO) 3 ] + via the reaction of 1,2-dihydronaphthalene with Fe 2 (CO) 9 followed by a hydride abstraction by trityl cation. However, this procedure was unsuccessful.…”
Section: Introductionmentioning
confidence: 99%