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Synthesis and Reactivity of Platinum(II) cis-Dialkyl, cis-Alkyl Chloro, and cis-Alkyl Hydrido Bis-N-heterocyclic Carbene Chelate Complexes
被引:12
|作者:
Brendel, Matthias
[1
]
Engelke, Rene
[1
]
Desai, Vidya G.
[1
]
Rominger, Frank
[1
]
Hofmann, Peter
[1
]
机构:
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词:
CARBON HYDROGEN-BONDS;
C-H;
THERMAL-DECOMPOSITION;
ROOM-TEMPERATURE;
ACTIVATION;
<BIS(DICYCLOHEXYLPHOSPHINO)ETHANE>PLATINUM(0);
CATALYSIS;
D O I:
10.1021/acs.organomet.5b00204
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Platinum(II) cis-dimethyl and cis-dineopentyl complexes bearing the alkyl-substituted bis-NHC ligands L-t-Bu, L-Me, and Li-Pr (Lt-Bu = 1,1'-di-tert-butyl-3,3'-methylenediimidazolin-2,2'-diylidene, LMe = 1,1'-dimethyl-3,3'-methylenediimidazolin-2,2'-diylidene, Li-Pr = 1,1'-diisopropyl-3,3'-methylenediimidazolin-2,2'-diylidene) as well as novel cis-alkyl chloro and cis-alkyl hydrido compounds were synthesized. The reactivity of the dimethyl complexes toward dichloromethane and methanol was investigated. Reductive elimination of alkanes from cis-alkyl hydrido complexes requires much higher temperatures than in related bisphosphine systems, which limits their applicability for the generation of reactive, bent platinum(0) d(10)-ML2 fragments for bond-activation chemistry. The platinum(II) complexes were characterized by NMR and IR spectroscopy, mass spectrometry, elemental analysis, and X-ray diffraction in most cases.
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页码:2870 / 2878
页数:9
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