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首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >The dinuclear ruthenium (II) complex [{Ru(Phen)_2}_2(HAT)]~(4+) (HAT=1, 4, 5, 8, 9, 12-hexaazatriphenylene), a new photoreagent for nucleobases and photoprobe for denatured DNA
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The dinuclear ruthenium (II) complex [{Ru(Phen)_2}_2(HAT)]~(4+) (HAT=1, 4, 5, 8, 9, 12-hexaazatriphenylene), a new photoreagent for nucleobases and photoprobe for denatured DNA

机译:双核钌(II)配合物[{Ru(Phen)_2} _2(HAT)]〜(4+)(HAT = 1,4,5,8,8,9,12-六氮杂苯并菲),一种用于核碱基和光探针的新型光试剂用于变性的DNA

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The photophysical and photochemical properties of a dinuclear ruthenium (II) complex, [{Ru(Phen)_2}_2(HAT)]~(4+) (Phen=1, 10-phenanthroline, HAT=1, 4, 5, 8, 9, 12-hexaazatriphenylene), have been examined in the presence of mononucleotides and different polynucleotides. Characteristic new features, not observed with monometallic ruthenium (II) complexes, appear with this dimeric compound. First it forms strong ion pairs with the mononucleotides, adenosine- and guanosine-5'-monophosphate, detected from the absorption and emission characteristics under steady state and time-resolved conditions. Secondly, under steady state illumination, very weak luminescence enhancements are induced by the addition of double stranded calf thymus DNA (CT-DNA) whereas important increases of emission occur by the addition of denatured CT-DNA. The dinuclear species may thus be regarded as an excallent photoprobe for denatured DNA. On the other hand, the same photoreactivity with the nucleobases as that of the monometallic TAP (1, 4, 5, 8-tetraazaphenanthrene) and HAT complexes has been retained by the dinuclear species, i.e. (i) a photoelectron transfer from guanosine monophosphate to the excited complex correlated with the formation of a photoproduct and (ii) a photoelectron transfer with DNA; in that case, however, this process is not systematically correlated with the formation of photoproduct in contrast to the monometallic species.
机译:双核钌(II)络合物[{Ru(Phen)_2} _2(HAT)]〜(4+)(Phen = 1,10-菲咯啉,HAT = 1,4,5,8)的光物理和光化学性质已经在单核苷酸和不同的多核苷酸存在下检查了(9,9,12-六氮杂三苯并)。这种二聚化合物具有单金属钌(II)配合物未观察到的特征性新特征。首先,从稳态和时间分辨条件下的吸收和发射特征检测,它与单核苷酸,腺苷5'和鸟苷5'-单磷酸形成强离子对。其次,在稳态照明下,通过添加双链小牛胸腺DNA(CT-DNA)可以诱导非常弱的发光增强作用,而通过添加变性的CT-DNA可以显着提高发光强度。双核物质因此可以被认为是变性DNA的超强光探针。另一方面,双核保留了与单金属TAP(1、4、5、8-四氮杂菲)和HAT配合物相同的与核碱基的光反应性,即(i)从鸟苷单磷酸到激发的复合物与光产物的形成和(ii)DNA的电子转移有关;然而,在这种情况下,与单金属物质相比,该过程与光产物的形成没有系统地相关。

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