Synthesis, Characterization, and Electronic Properties of Porphyrins. Conjugated with N-Heterocyclic Carbene (NHC)-Gold(I) Complexes
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作者:
Longevial, Jean-Francois
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CNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, FranceCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Longevial, Jean-Francois
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Langlois, Adam
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Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, CanadaCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Langlois, Adam
[2
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Buisson, Antoine
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Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, CanadaCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Buisson, Antoine
[2
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Devillers, Charles H.
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ICMUB, Bourgogne Franche Comte, UMR CNRS 6302, F-21000 Dijon, FranceCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Devillers, Charles H.
[3
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Clement, Sebastien
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CNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, FranceCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Clement, Sebastien
[1
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van der Lee, Arie
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CNRS ENSCM UM, Inst Europeen Membranes, UMR 5635, CC 047,Pl E Bataillon, F-34095 Montpellier 05, FranceCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
van der Lee, Arie
[4
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Harvey, Pierre D.
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Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, CanadaCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Harvey, Pierre D.
[2
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Richeter, Sebastien
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CNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, FranceCNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Richeter, Sebastien
[1
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机构:
[1] CNRS ENSCM UM, ICGM, UMR 5253, CC 1701,Pl E Bataillon, F-34095 Montpellier 05, France
Porphyrins fused to peripheral N-heterocyclic carbenes (NHC) across two neighboring beta,beta-pyrrolic positions were used for the synthesis of different mono- and bis-carbenic gold(I) complexes. These studies also revealed how it is possible to modulate the reactivity of the peripheral NHC by deprotonating the inner NH groups of the fused free base porphyrin core. All complexes were fully characterized and displayed high stability, allowing the formation of mono-carbenic and also stable homoleptic and heteroleptic bis-carbenic Au(I) complexes. Optical and electrochemical properties of bis-catbenic Au(I) revealed no or weak electronic communication between the porphyrins, which behave as two independent groups.