Derosa Frank, Bu Xianhui, Ford Peter C
Department of Chemistry and Biochemistry, University of California at Santa Barbara, Santa Barbara, California 93106-9510.
Inorg Chem. 2005 Jun 13;44(12):4157-65. doi: 10.1021/ic048311o.
Several new dinitritochromium(III) complexes of the type trans-[Cr(L)(ONO)(2)]BF(4), where L is a derivative of the macrocyclic ligand cyclam having pendant aromatic chromophores attached (L = 5,7-dimethyl-6-(substituted)-1,4,8,11-tetraazacyclotetradecane), have been prepared and characterized. Photoexcitation of aqueous solutions containing these complexes at wavelengths corresponding to the pendant chromophore absorption bands led to the generation of NO as detected by an electrochemical sensor. Photophysical data show that the expected fluorescence of the pendant chromophores is largely quenched when the macrocyclic ligand is coordinated to these Cr(III) centers, and this is interpreted in terms of fast energy transfer processes from the ligand-centered pipi states to the Cr(III)-centered ligand field states leading to subsequent cleavage of the Cr(III)-coordinated nitrito ligand. Thus, the chromophores tethered to the coordinated cyclam serve as light-gathering antennae for the intramolecular sensitization of the NO-generating photoreactions at the metal center.
已制备并表征了几种新型的反式-[Cr(L)(ONO)(2)]BF(4)型二亚硝基铬(III)配合物,其中L是带有侧链芳香发色团的大环配体环胺的衍生物(L = 5,7-二甲基-6-(取代基)-1,4,8,11-四氮杂环十四烷)。在与侧链发色团吸收带对应的波长下对含有这些配合物的水溶液进行光激发,通过电化学传感器检测到生成了NO。光物理数据表明,当大环配体与这些Cr(III)中心配位时,侧链发色团预期的荧光在很大程度上被猝灭,这可以通过从配体中心的ππ态到Cr(III)中心的配体场态的快速能量转移过程来解释,该过程导致随后Cr(III)配位的亚硝基配体的裂解。因此,连接到配位环胺上的发色团作为光收集天线,用于在金属中心对产生NO的光反应进行分子内敏化。