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Reversible carbon-carbon bond formation in organolanthanide systems. Preparation and properties of lanthanide acetylides [Cp*{sub 2}LnC{triple_bond}CR]{sub n} and their rearrangement products [Cp*{sub 2}Ln]{sub 2}({mu}-{eta}{sup 2}:{eta}{sup 2}-RC{sub 4}R) (Ln = La, Ce, R = Alkyl)

Journal Article · · Organometallics
; ;  [1]
  1. Univ. of Groningen (Netherlands); and others

Lanthanide carbyls Cp*{sub 2}LnCH(SiMe{sub 3}){sub 2}{sup 1} (1, Ln=Ce;2, Ln=La) react with terminal alkynes HC{triple_bond}CR (R = Me, t-Bu) to yield oligomeric acetylides [Cp*{sub 2}LnC{triple_bond}CR]{sub n} (3, Ln = Ce, R = Me; 4, Ln = La, R = Me; 5, Ln = Ce, R = t-Bu). The acetylides are not stable in solution and rearrange to give the carbon-carbon coupled products, [Cp*{sub 2}Ln]{sub 2}({mu}-{eta}{sup 2}:{eta}{sup 2}-RC{sub 4}R) (6, Ln = Ce, R = Me; 7, Ln = La, R = Me; 8, Ln = Ce, R = t-Bu). Thermodynamic and kinetic studies of the C-C coupling process were studied as were the structures of 6 and 8 via XRD.

Sponsoring Organization:
USDOE
OSTI ID:
433548
Journal Information:
Organometallics, Journal Name: Organometallics Journal Issue: 7 Vol. 12; ISSN 0276-7333; ISSN ORGND7
Country of Publication:
United States
Language:
English