首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >NEW CHARGE TRANSFER LUMINESCENT POLYMETALLIC COMPLEXES OF RHODIUM(III), IRIDIUM(III), AND RUTHENIUM(II) WITH THE BRIDGING LIGAND 1,4,5,8,9,12-HEXAAZATRIPHENYLENE
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NEW CHARGE TRANSFER LUMINESCENT POLYMETALLIC COMPLEXES OF RHODIUM(III), IRIDIUM(III), AND RUTHENIUM(II) WITH THE BRIDGING LIGAND 1,4,5,8,9,12-HEXAAZATRIPHENYLENE

机译:带有桥接配体1,4,5,8,9,12-六氮杂三苯的铑(III),铱(III)和AND(II)的新型电荷转移发光多金属配合物

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New emitting binuclear (Rh)(i)-(Ru)(2-i) (i = 1, 2), (Ir)-(Ru), and trinuclear (Rh)(i)-(Ru)(3-i) (i = 1, 2, 3) complexes assembled by the trischelating bridging ligand HAT (1,4,5,8,9,12-hexaazatriphenylene), have been synthesized. Their characterization by mass spectrometry (FAB and electrospray) is in accordance with their expected structure, where Rh(PPY)(2)(+) (or Ir(PPY)(2)(+)) and Ru(BPY)(2)(2+) correspond to the building blocks (PPY is the ortho-C-deprotonated form of 2-phenylpyridine and BPY is 2,2'-bipyridine). The HPLC data of these polymetallic compounds reveal that the trimetallic homo- and heteronuclear complexes are not stable under the chromatographic conditions and in some organic solvents. Therefore, the electrochemical and photophysical data are given only for the bimetallic compounds, stable under these conditions. Under electrochemical oxidation, the bimetallic Rh(III) complex shows one irreversible wave in the accessible potential range, while the heteronuclear Rh(III)-Ru(II) and Ir(III)-Ru(II) compounds exhibit an irreversible process followed by a reversible wave. For the bimetallic (homo- and heteronuclear) complexes, the first reduction wave involves a HAT-centered pi* orbital. On the basis of the electrochemical, luminescence and resonance Raman data, the lowest electronic transitions are CT (charge transfer) transitions involving the bridging HAT. These transitions have an MLCT (metal to ligand charge transfer) type for the Ru(II) moiety and a SBLCT (sigma-bond to ligand charge transfer) character for the Rh(III) unit; in the case of the Ir(III) moiety there is a strong admixture of SBLCT and MLCT character. An energy transfer would take place from the Ru-HAT (3)MLCT state towards the Ir-HAT (3)SBLCT (mixed with (3)MLCT character) in the Ir(III)-Ru(II) compound. For the Rh(III)-Ru(II) complex the nature of the luminescent excited state (Ru-HAT (3)MLCT or Rh-HAT (3)SBLCT) cannot be unambiguously determined. [References: 43]
机译:新发射的双核(Rh)(i)-(Ru)(2-i)(i = 1,2),(Ir)-(Ru)和三核(Rh)(i)-(Ru)(3-i) )已经合成了由三配位桥键配体HAT(1,4,5,8,9,12-六氮杂苯并菲)组装的(i = 1,2,3)配合物。通过质谱(FAB和电喷雾)对其进行表征符合其预期的结构,其中Rh(PPY)(2)(+)(或Ir(PPY)(2)(+))和Ru(BPY)(2) (2+)对应于结构单元(PPY是2-苯基吡啶的邻-C-去质子化形式,BPY是2,2'-联吡啶)。这些多金属化合物的HPLC数据表明,三金属同核和异核配合物在色谱条件下和某些有机溶剂中不稳定。因此,仅给出了在这些条件下稳定的双金属化合物的电化学和光物理数据。在电化学氧化作用下,双金属Rh(III)络合物在可及电位范围内显示出一个不可逆的波,而异核Rh(III)-Ru(II)和Ir(III)-Ru(II)化合物表现出不可逆的过程,随后是可逆的波浪。对于双金属(同核和异核)配合物,第一个还原波涉及以HAT为中心的pi *轨道。根据电化学,发光和共振拉曼数据,最低的电子跃迁是涉及桥接HAT的CT(电荷转移)跃迁。这些过渡具有Ru(II)部分的MLCT(金属至配体电荷转移)类型和Rh(III)单元的SBLCT(σ键至配体电荷转移)特征。在Ir(III)部分的情况下,存在SBLCT和MLCT特性的强烈混合物。在Ir(III)-Ru(II)化合物中,能量将从Ru-HAT(3)MLCT状态向Ir-HAT(3)SBLCT(与(3)MLCT特性混合)发生。对于Rh(III)-Ru(II)配合物,不能明确确定发光激发态(Ru-HAT(3)MLCT或Rh-HAT(3)SBLCT)的性质。 [参考:43]

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