Iodination of cyclo‐E5‐Complexes (E=P, As). Issue 37 (9th July 2020)
- Record Type:
- Journal Article
- Title:
- Iodination of cyclo‐E5‐Complexes (E=P, As). Issue 37 (9th July 2020)
- Main Title:
- Iodination of cyclo‐E5‐Complexes (E=P, As)
- Authors:
- Brake, Helena
Peresypkina, Eugenia
Virovets, Alexander V.
Piesch, Martin
Kremer, Werner
Zimmermann, Lisa
Klimas, Christian
Scheer, Manfred - Abstract:
- Abstract: In a high‐yield one‐pot synthesis, the reactions of [Cp*M(η 5 ‐P5 )] (M=Fe (1 ), Ru (2 )) with I2 resulted in the selective formation of [Cp*MP6 I6 ] + salts (3, 4 ). The products comprise unprecedented all‐ cis tripodal triphosphino‐cyclotriphosphine ligands. The iodination of [Cp*Fe(η 5 ‐As5 )] (6 ) gave, in addition to [Fe(CH3 CN)6 ] 2+ salts of the rare [As6 I8 ] 2− (in 7 ) and [As4 I14 ] 2− (in 8 ) anions, the first di‐cationic Fe‐As triple decker complex [(Cp*Fe)2 (μ, η 5:5 ‐As5 )][As6 I8 ] (9 ). In contrast, the iodination of [Cp*Ru(η 5 ‐As5 )] (10 ) did not result in the full cleavage of the M−As bonds. Instead, a number of dinuclear complexes were obtained: [(Cp*Ru)2 (μ, η 5:5 ‐As5 )][As6 I8 ]0.5 (11 ) represents the first Ru‐As5 triple decker complex, thus completing the series of monocationic complexes [(Cp R M)2 (μ, η 5:5 ‐E5 )] + (M=Fe, Ru; E=P, As). [(Cp*Ru)2 As8 I6 ] (12 ) crystallizes as a racemic mixture of both enantiomers, while [(Cp*Ru)2 As4 I4 ] (13 ) crystallizes as a symmetric and an asymmetric isomer and features a unique tetramer of {AsI} arsinidene units as a middle deck. Abstract : The iodination of cyclo ‐E5 complexes was introduced for the synthesis of polypnictogen complexes. In the reaction of [Cp*M(η 5 ‐P5 )] (M=Fe, Ru) with iodine, [Cp*MP6 I6 ] + cations with tripodal cyclo ‐{P(PI2 )}3 ligands were formed. With cyclo ‐As5 complexes, the first di‐cationic Fe‐As triple decker, the first monocationic Ru‐As5 triple decker and twoAbstract: In a high‐yield one‐pot synthesis, the reactions of [Cp*M(η 5 ‐P5 )] (M=Fe (1 ), Ru (2 )) with I2 resulted in the selective formation of [Cp*MP6 I6 ] + salts (3, 4 ). The products comprise unprecedented all‐ cis tripodal triphosphino‐cyclotriphosphine ligands. The iodination of [Cp*Fe(η 5 ‐As5 )] (6 ) gave, in addition to [Fe(CH3 CN)6 ] 2+ salts of the rare [As6 I8 ] 2− (in 7 ) and [As4 I14 ] 2− (in 8 ) anions, the first di‐cationic Fe‐As triple decker complex [(Cp*Fe)2 (μ, η 5:5 ‐As5 )][As6 I8 ] (9 ). In contrast, the iodination of [Cp*Ru(η 5 ‐As5 )] (10 ) did not result in the full cleavage of the M−As bonds. Instead, a number of dinuclear complexes were obtained: [(Cp*Ru)2 (μ, η 5:5 ‐As5 )][As6 I8 ]0.5 (11 ) represents the first Ru‐As5 triple decker complex, thus completing the series of monocationic complexes [(Cp R M)2 (μ, η 5:5 ‐E5 )] + (M=Fe, Ru; E=P, As). [(Cp*Ru)2 As8 I6 ] (12 ) crystallizes as a racemic mixture of both enantiomers, while [(Cp*Ru)2 As4 I4 ] (13 ) crystallizes as a symmetric and an asymmetric isomer and features a unique tetramer of {AsI} arsinidene units as a middle deck. Abstract : The iodination of cyclo ‐E5 complexes was introduced for the synthesis of polypnictogen complexes. In the reaction of [Cp*M(η 5 ‐P5 )] (M=Fe, Ru) with iodine, [Cp*MP6 I6 ] + cations with tripodal cyclo ‐{P(PI2 )}3 ligands were formed. With cyclo ‐As5 complexes, the first di‐cationic Fe‐As triple decker, the first monocationic Ru‐As5 triple decker and two isomers of a complex with a unique tetramer of iodoarsinidene units were obtained. … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 59:Issue 37(2020)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 59:Issue 37(2020)
- Issue Display:
- Volume 59, Issue 37 (2020)
- Year:
- 2020
- Volume:
- 59
- Issue:
- 37
- Issue Sort Value:
- 2020-0059-0037-0000
- Page Start:
- 16241
- Page End:
- 16246
- Publication Date:
- 2020-07-09
- Subjects:
- arsinidenes -- iodination -- oxidation -- polyphosphorus ligands -- polypnictogen complexes
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.202004812 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20660.xml