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Fig. 2 (A) Schematic diagram of synthesis of gold nanoclusters from the Au 11 (PPh 3 ) 8 Cl 3 cluster
precursor 1. Synthesis conditions: ( a ) Ligand exchange of 1 in CHCl 3 at 55 C with excess
octadecanethiol produces the thiol-stabilized particle 2;( b ) Interfacial (CHCl 3 /H 2 O) ligand
exchange of 1 at 55 C with ( N , N -dimethylamino)ethanethiol hydrochloride produces the cationic
thiol-stabilized particle 3 in a single step; ( c ) Interfacial (CHCl 3 /H 2 O) ligand exchange of 1 at
55 C with sodium 2-mercaptoethanesulfonate (MESA) produces the anionic particle 4, which
contains a mixed ligand shell; ( d ) Treatment of 4 with excess MESA in 1:1 THF/H 2 O yields
particle 5 containing only MESA in the ligand shell. (B) UV-Vis spectra of the gold precursor and
the formed nanoclusters through ligand exchange process as described in A.( a ) precursor cluster 1;
( b ) cluster 2;( c ) cluster 3;( d ) cluster 5. Reprinted from [ 58 ] with permission by the American
Chemical Society
protected by 4, 4, 4-phosphinidynetri(benzenemethanamine). However, these
clusters are normally not stable and are prone to oxidative decomposition when
exposed to ambient conditions. In order to overcome such problem, Hutchison and
coworkers [ 58 ] synthesized stable Au 11 nanoclusters protected by alkanethiols
through an exchange-reaction process. As shown in Fig. 2A , such ligand exchange
strategy could be applied to the preparation of different
thiol-stabilized Au
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