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Further Evidence for 'Extended' Cumulene Complexes: Derivatives from Reactions with Halide Anions and Water.

Authors :
Hall MR
Steen RR
Korb M
Sobolev AN
Moggach SA
Lynam JM
Low PJ
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2020 Jun 05; Vol. 26 (32), pp. 7226-7234. Date of Electronic Publication: 2020 Apr 28.
Publication Year :
2020

Abstract

Reactions of [Ru{C=C(H)-1,4-C <subscript>6</subscript> H <subscript>4</subscript> C≡CH}(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp]BF <subscript>4</subscript> ([1 a]BF <subscript>4</subscript> ) with hydrohalic acids, HX, results in the formation of [Ru{C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C(X)=CH <subscript>2</subscript> }(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp] [X=Cl (2 a-Cl), Br (2 a-Br)], arising from facile Markovnikov addition of halide anions to the putative quinoidal cumulene cation [Ru(=C=C=C <subscript>6</subscript> H <subscript>4</subscript> =C=CH <subscript>2</subscript> )(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp] <superscript>+</superscript> . Similarly, [M{C=C(H)-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C≡CH}(LL)Cp ]BF <subscript>4</subscript> [M(LL)Cp'=Ru(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp ([1 a]BF <subscript>4</subscript> ); Ru(dppe)Cp* ([1 b]BF <subscript>4</subscript> ); Fe(dppe)Cp ([1 c]BF <subscript>4</subscript> ); Fe(dppe)Cp* ([1 d]BF <subscript>4</subscript> )] react with H <superscript>+</superscript> /H <subscript>2</subscript> O to give the acyl-functionalised phenylacetylide complexes [M{C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C(=O)CH <subscript>3</subscript> }(LL)Cp'] (3 a-d) after workup. The Markovnikov addition of the nucleophile to the remote alkyne in the cations [1 a-d] <superscript>+</superscript> is difficult to rationalise from the vinylidene form of the precursor and is much more satisfactorily explained from initial isomerisation to the quinoidal cumulene complexes [M(=C=C=C <subscript>6</subscript> H <subscript>4</subscript> =C=CH <subscript>2</subscript> )(LL)Cp'] <superscript>+</superscript> prior to attack at the more exposed, remote quaternary carbon. Thus, whilst representative acetylide complexes [Ru(C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C≡CH)(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp] (4 a) and [Ru(C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C≡CH)(dppe)Cp*] (4 b) reacted with the relatively small electrophiles [CN] <superscript>+</superscript> and [C <subscript>7</subscript> H <subscript>7</subscript> ] <superscript>+</superscript> at the β-carbon to give the expected vinylidene complexes, the bulky trityl ([CPh <subscript>3</subscript> ] <superscript>+</superscript> ) electrophile reacted with [M(C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C≡CH)(LL)Cp'] [M(LL)Cp'=Ru(PPh <subscript>3</subscript> ) <subscript>2</subscript> Cp (4 a); Ru(dppe)Cp* (4 b); Fe(dppe)Cp (4 c); Fe(dppe)Cp* (4 d)] at the more exposed remote end of the carbon-rich ligand to give the putative quinoidal cumulene complexes [M{C=C=C <subscript>6</subscript> H <subscript>4</subscript> =C=C(H)CPh <subscript>3</subscript> }(LL)Cp'] <superscript>+</superscript> , which were isolated as the water adducts [M{C≡C-1,4-C <subscript>6</subscript> H <subscript>4</subscript> -C(=O)CH <subscript>2</subscript> CPh <subscript>3</subscript> }(LL)Cp'] (6 a-d). Evincing the scope of the formation of such extended cumulenes from ethynyl-substituted arylvinylene precursors, the rather reactive half-sandwich (5-ethynyl-2-thienyl)vinylidene complexes [M{C=C(H)-2,5- <superscript>c</superscript> C <subscript>4</subscript> H <subscript>2</subscript> S-C≡CH}(LL)Cp']BF <subscript>4</subscript> ([7 a-d]BF <subscript>4</subscript> add water readily to give [M{C≡C-2,5- <superscript>c</superscript> C <subscript>4</subscript> H <subscript>2</subscript> S-C(=O)CH <subscript>3</subscript> }(LL)Cp'] (8 a-d)].<br /> (© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3765
Volume :
26
Issue :
32
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
32048354
Full Text :
https://doi.org/10.1002/chem.201905399