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Synthesis and Characterization of Gold(III) Complexes Bearing a Picoline-functionalized N-Heterocyclic Carbene
被引:17
|作者:
Topf, Christoph
[1
]
Hirtenlehner, Christa
[1
]
Fleck, Michel
[2
]
List, Manuela
[3
]
Monkowius, Uwe
[1
]
机构:
[1] Johannes Kepler Univ Linz, Inst Anorgan Chem, A-4040 Linz, Austria
[2] Univ Vienna, Geozentrum, Inst Mineral & Kristallog, A-1090 Vienna, Austria
[3] Johannes Kepler Univ Linz, Inst Chem Technol Organ Stoffe, A-4040 Linz, Austria
来源:
关键词:
N-Heterocyclic carbenes;
Silver;
Gold;
Crystal Structure;
Picoline;
SUBSTITUTED NHC LIGAND;
OLEFIN POLYMERIZATION;
CATALYTIC-ACTIVITY;
GOLD CATALYSIS;
AU(I);
SILVER(I);
AG(I);
DINUCLEAR;
ALKYNES;
CYCLOISOMERIZATION;
D O I:
10.1002/zaac.201100341
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
3-Methyl-1-(2-picolyl)-imidazolium chloride (1) has been synthesized and used as a precursor for the preparation of the (NHC)AgCl complex [NHC = 3-methyl-1-(2-picolyl)imidazol-2-ylidene] (2). Transmetalation of 2 with (tht)AuBr (tht = tetrahydrothiophene) yields the corresponding (NHC)AuBr complex 3, which is further oxidized by Br2 to give the (NHC)AuBr3 compound 4. Treatment of 4 with one equivalent of solid AgBF4 affords the [(NHC)AuBr2][BF4] congener 5 as a pale green, crystalline powder. The structure of 4 and 5 were determined by single-crystal X-ray diffraction, revealing for 5 a ?-N-coordination of the AuIII atom by the picolyl nitrogen atom. Further attempts to exchange all bromides by carboxylates results in the reduction to the dimeric AuI compound [(NHC)2Au2][BF4]2, 6.
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页码:2129 / 2134
页数:6
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