scholarly journals Gold cluster compounds

Gold Bulletin ◽  
1984 ◽  
Vol 17 (1) ◽  
pp. 5-12 ◽  
Author(s):  
D. Michael P. Mingos
2018 ◽  
Vol 9 (25) ◽  
pp. 5614-5622 ◽  
Author(s):  
Ping Guo ◽  
Biao Yang ◽  
Li Zhang ◽  
Liang Zhao

Three chiral gold cluster compounds are herein selected to probe how structural factors influence the cluster stability upon heating.


1995 ◽  
Vol 143 ◽  
pp. 219-263 ◽  
Author(s):  
Louis H. Pignolet ◽  
Mark A. Aubart ◽  
Kathryn L. Craighead ◽  
Rachael A.T. Gould ◽  
Don A. Krogstad ◽  
...  

2010 ◽  
Vol 100 (10) ◽  
pp. 375-377 ◽  
Author(s):  
F. A. Vollenbroek ◽  
J. W. A. van der Velden ◽  
J. J. Bour ◽  
J. M. Trooster

The bonding in tertiary phosphine cluster compounds of gold is sufficiently straightforward to permit an effective interaction between theoretical concepts developed from semi-empirical molecular orbital calculations and synthetic and structural chemistry. At the simplest conceptual level the isolobal nature of the Au(PR 3 ) fragment and either the CH 3 or H radicals provides a basis for understanding the structures of a wide range of homonuclear and heteronuclear clusters, e.g. Os 3 (CO) 10 - H(AuPPh 3 ) and (OG) 5 VAu 3 (PPh 3 ) 3 . However, this simplified approach neglects some secondary gold-gold interactions between adjacent gold atoms, which arise from the availability of the higher-lying gold 6p orbitals. In low-nuclearity clusters tetrahedral fragments, which permit the effective formation of four-centre two electron bonds between the Au(PR 3 ) fragments, are preferred to larger deltahedra. In higher-nuclearity clusters the stabilities of the clusters depend on the presence of a central gold atom that provides strong radial gold-gold bonding. The relative importance of the radial and tangential components to the total bonding has been effectively demonstrated by a structural comparison of alternative Au 9 (PR 3 )3/8+ clusters. The predictive capability of the theoretical approach has been demonstrated by the synthesis and structural characterization of the icosahedral cluster [Au 13 Cl 2 (PMe 2 Ph) 10 ]3+.


2000 ◽  
Vol 6 (S2) ◽  
pp. 326-327
Author(s):  
J.F. Hainfeld ◽  
R.D. Powell ◽  
F.R. Furuya ◽  
J.S. Wall

Gold clusters are gold compounds with a core of gold atoms and organic groups covalently bound to the surface gold atoms. An example is undecagold, Au11(P(C6H5)3)7, whose structure was solved by x-ray crystallography using 3-dimensional crystals. These differ from colloidal gold, which are suspensions of metal particles, usually formed by metal ion reduction; although the particles may be approximately the same size, they vary due to the statistical process of formation. Gold clusters are compounds with a definite formula, and should all be perfectly identical. However, it is known that there is a family of stable gold cluster compounds, such as Au6, Au11, Au13, AU55, Au67, etc. In a given preparation of gold clusters, there is usually some mixture of these, thus leading to some size variation. Methods such as gel filtration column chromatography and ultrafiltration can be used to separate most of these species, so that relatively pure preparations may be achieved.


1991 ◽  
Vol 30 (25) ◽  
pp. 4704-4709 ◽  
Author(s):  
M. F. J. Schoondergang ◽  
J. J. Bour ◽  
P. P. J. Schlebos ◽  
A. W. P. Vermeer ◽  
W. P. Bosman ◽  
...  

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