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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Synthesis, crystal structure and photoluminescence of the salts Cation(+) [M(caffeine)Cl](-) with Cation(+) = (NBu4+)-Bu-n, AsPh4+ and M = Zn(II), Pt(II)
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Synthesis, crystal structure and photoluminescence of the salts Cation(+) [M(caffeine)Cl](-) with Cation(+) = (NBu4+)-Bu-n, AsPh4+ and M = Zn(II), Pt(II)

机译:阳离子(+)=(NBU4 +) - BU-N,Asph4 +和M = Zn(II),Pt(II),盐阳离子(+)[M(咖啡因)Cl]( - )的合成,晶体结构和光致发光 - ( - ),Pt(II)

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摘要

The salts ((NBu4)-Bu-n)[Zn(caffeine)Cl-3] and (AsPh4) [Pt(caffeine)Cl-3] were prepared and their crystal structures determined by single crystal X-ray diffraction. The free ligand caffeine, as well as the complex anions [M(II)(caffeine)Cl-3](-) with M=Zn and Pt show an absorption spectrum with an intense band at lambda(max) = 275 nm, which is attributed to an IL pi-pi* transition of the caffeine. A second band at ca. 300 nm is much weaker and largely obscured by the pi-pi* band. This second band is assigned to an IL n-pi* transition. Both complex anions exhibit a photoluminescence (fluorescence), which originates from the n-pi* state. The position of the n-pi* state is recognized by the excitation band which distinctly overlaps with the fluorescence band.
机译:制备盐((NBU4)-Bu-N)[Zn(咖啡因)Cl-3]和(asPH4)[Pt(咖啡因)Cl-3],并通过单晶X射线衍射确定它们的晶体结构。 自由配体咖啡因以及具有M = Zn和PT的复合阴离子[M(II)(咖啡因)Cl-3]( - )显示出在Lambda(MAX)= 275nm处的吸收光谱,其 归因于咖啡因的IL PI-PI *过渡。 在加利福尼亚州的第二频段。 300nm弱得较弱,主要被PI-PI *乐队模糊不清。 该第二频带被分配给IL N-PI *转换。 两个复合阴离子都表现出光致发光(荧光),其源自N-PI *状态。 N-PI *状态的位置被激励带识别,其与荧光带清晰地重叠。

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