Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates
type: CreativeWork
description: The development of alkali-metal arylsilanolates as notable organometallic reagents for the preparation of biaryls has been realized through in depth mechanistic and preparative studies. The alkali-metal salts (potassium and sodium) of a large number of arylsilanols undergo smooth cross-coupling with a wide range of aromatic bromides and chlorides. The critical feature for the success of these coupling reactions and their considerable scope is the use of bis(tri-tert-butylphosphine)palladium. Additionally, these studies have identified the use of phosphine oxides (e.g. triphenylphosphine oxide) as useful ligands for palladium-catalyzed cross-coupling reactions. This serendipitous discovery was founded on kinetic experiments which revealed a significant rate enhancement employing these species as ligands for palladium. Later, these ligands were implemented in the reaction of arylsilanolates for the preparation of biaryl products. The mechanism of palladium-catalyzed cross-coupling reactions of alkali-metal organosilanolates has also been investigated. Under catalysis by (t-Bu3P)2Pd, the coupling with aryl bromides displays the following rate equation: rate = kobs[R3SiOK]0[ArylBr]0, with kobs = k[(t-Bu3P)2Pd]0.98. An independent study of the individual steps of the catalytic cycle has revealed a dual mechanistic pathway. The transmetalation can occur by a thermal process via an 8-Si-4 intermediate without the need for anionic activation. Additionally, arylsilanolates can serve as activators for transmetalation via a hypervalent 10-Si-5 siliconate intermediate. The independent isolation of the putative arylpalladium(II) arylsilanolate intermediate has confirmed the generation of the Pd-O-Si linkage prior to transmetalation. The unique opportunity to isolate a pretransmetalation intermediate has allowed the transmetalation step to be further refined through a detailed Hammett analysis which has demonstrated that increased electron-density about the arylsilanolate nucleop…
abstract: The development of alkali-metal arylsilanolates as notable organometallic reagents for the preparation of biaryls has been realized through in depth mechanistic and preparative studies. The alkali-metal salts (potassium and sodium) of a large number of arylsilanols undergo smooth cross-coupling with a wide range of aromatic bromides and chlorides. The critical feature for the success of these coupling reactions and their considerable scope is the use of bis(tri-tert-butylphosphine)palladium. Additionally, these studies have identified the use of phosphine oxides (e.g. triphenylphosphine oxide) as useful ligands for palladium-catalyzed cross-coupling reactions. This serendipitous discovery was founded on kinetic experiments which revealed a significant rate enhancement employing these species as ligands for palladium. Later, these ligands were implemented in the reaction of arylsilanolates for the preparation of biaryl products. The mechanism of palladium-catalyzed cross-coupling reactions of alkali-metal organosilanolates has also been investigated. Under catalysis by (t-Bu3P)2Pd, the coupling with aryl bromides displays the following rate equation: rate = kobs[R3SiOK]0[ArylBr]0, with kobs = k[(t-Bu3P)2Pd]0.98. An independent study of the individual steps of the catalytic cycle has revealed a dual mechanistic pathway. The transmetalation can occur by a thermal process via an 8-Si-4 intermediate without the need for anionic activation. Additionally, arylsilanolates can serve as activators for transmetalation via a hypervalent 10-Si-5 siliconate intermediate. The independent isolation of the putative arylpalladium(II) arylsilanolate intermediate has confirmed the generation of the Pd-O-Si linkage prior to transmetalation. The unique opportunity to isolate a pretransmetalation intermediate has allowed the transmetalation step to be further refined through a detailed Hammett analysis which has demonstrated that increased electron-density about the arylsilanolate nucleop…
author: Smith, Russell C.
language: en
keywords: arylsilanolates, biaryls, mechanism, palladium
date published: 2010-08-20T17:59:12Z
date modified: 2026-07-22T22:25:09Z
provider: University of Illinois - Urbana-Champaign
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Illinois at Urbana-Champaign

PropertyValue
property ID: Handle
value: http://hdl.handle.net/2142/16830