Synthesis, reactivity and catalytic activity of Au-PAd complexes.

Dalton Trans

Department of Chemistry and Center for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S-3), 9000 Ghent, Belgium.

Published: October 2020


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Tri(1-adamantyl)phosphine (PAd3) possesses unique steric and electronic properties positioning it at the border between tertiary phosphines and N-heterocyclic carbenes (NHC). Novel Au-PAd3 complexes were synthesized from the known [Au(PAd3)Cl]. We have optimised reaction conditions for the synthesis of this useful synthon in order to circumvent the formation of the [Au(PAd3)2]Cl. [Au(PAd3)Cl] was used to access a number of derivatives and some were deployed as catalysts. The hydration of alkynes was targeted to gauge the reactivity of Au-PAd3 complexes and permit comparison with NHC and tertiary phosphine congeners.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d0dt03330hDOI Listing

Publication Analysis

Top Keywords

au-pad3 complexes
8
synthesis reactivity
4
reactivity catalytic
4
catalytic activity
4
activity au-pad
4
au-pad complexes
4
complexes tri1-adamantylphosphine
4
tri1-adamantylphosphine pad3
4
pad3 possesses
4
possesses unique
4

Similar Publications

Synthesis, reactivity and catalytic activity of Au-PAd complexes.

Dalton Trans

October 2020

Department of Chemistry and Center for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S-3), 9000 Ghent, Belgium.

Tri(1-adamantyl)phosphine (PAd3) possesses unique steric and electronic properties positioning it at the border between tertiary phosphines and N-heterocyclic carbenes (NHC). Novel Au-PAd3 complexes were synthesized from the known [Au(PAd3)Cl]. We have optimised reaction conditions for the synthesis of this useful synthon in order to circumvent the formation of the [Au(PAd3)2]Cl.

View Article and Find Full Text PDF