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Gold phosphine complex

Hydroamination of olefins has received considerable attention this year as a route to functionalized piperidines and spiropiperidines, particularly in regard to the investigation of new catalysts. In the synthesis of spiro-piperidines, two new mild and more general intramolecular hydroamination protocols were developed this year. One protocol uses a cationic gold-phosphine complex (Au[P(fBu)2(o-biphenyl)]Cl) as the catalyst... [Pg.335]

Luminescence has been noted [88] in numerous gold phosphine complexes. [Pg.295]

TABLE 7. 31P NMR shifts41 and coordination chemical shifts for gold-phosphine complexes... [Pg.90]

One may conclude that Au5d orbitals should not be regarded as core, but rather as valence orbitals which contribute significantly to bonding in gold-phosphine complexes. [Pg.111]

A major hurdle towards understanding the unusual low temperature CO oxidation activities of supported Au catalysis is that there is a wide variation in the reported CO oxidation activities over these catalysts [5]. This arises because these catalysts are very sensitive to the preparation procedures. Most supported Au catalysts are prepared with the chloride-containing chloroauric acid precursor, although there have been recent attempts to prepare these catalysts with precursors such as dimethyl gold acetonate [6], gold-phosphine complexes [7], and gold ethylene diamine complexes [8]. This discussion will focus on the complications that arise with chloride-containing precursors. [Pg.152]

Many gold phosphine complexes have been found to be potent cytotoxic agents, to have antitumor activity against P388 leukaemia and to be active against a spectrum of transplantable tumour models . It has been of particular interest to obtain some of them labeUed with radioactive isotopes of gold and carbon for cellular, binding, metabolism and biodistribution studies. [Pg.504]


See other pages where Gold phosphine complex is mentioned: [Pg.295]    [Pg.307]    [Pg.112]    [Pg.314]    [Pg.520]    [Pg.16]    [Pg.40]    [Pg.290]    [Pg.90]    [Pg.90]    [Pg.111]    [Pg.177]    [Pg.164]    [Pg.176]    [Pg.374]    [Pg.362]    [Pg.295]    [Pg.67]    [Pg.89]    [Pg.89]    [Pg.780]    [Pg.786]    [Pg.520]    [Pg.241]    [Pg.545]    [Pg.93]    [Pg.323]    [Pg.67]    [Pg.89]    [Pg.89]    [Pg.786]    [Pg.151]    [Pg.152]   
See also in sourсe #XX -- [ Pg.93 ]

See also in sourсe #XX -- [ Pg.93 ]




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Complexes gold

Deposition of gold-phosphine complexes

Gold complexes phosphine methyls

Gold complexes with phosphines

Gold phosphine complexes, reactions with

Gold phosphine complexes, reactions with metal clusters

Gold(I) Complexes with Monodentate Phosphines

Luminescent gold phosphine complexes

Phosphine triethyl-, gold-osmium complex

Phosphine-gold® complexes luminescence

Phosphine-gold® complexes synthesis

Phosphines gold sulfide complexes

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