Takani Masako, Yajima Tatsuo, Masuda Hideki, Yamauchi Osamu
Faculty of Pharmaceutical Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
J Inorg Biochem. 2002 Jul 25;91(1):139-50. doi: 10.1016/s0162-0134(02)00439-7.
The metal binding properties of a phenolic lichen substance usnic acid (UA) and its acetyl and enamine derivatives 9-O-acetylusnic acid (MAUA), 7,9-di-O-acetylusnic acid (DAUA), Delta(2,11)-enaminousnic acid (EUA), and N-substituted Delta(2,11)-enaminousnic acids have been studied by synthetic and spectroscopic methods, and the structures of copper(II) and palladium(II) complexes have been established by the X-ray diffraction method. Cu(II) reacted with UA and DAUA to give the binary complexes Cu(UA)(2) x H(2)O and Cu(DAUA)(2), respectively, and Cu(bpy) (bpy=2,2'-bipyridine) formed ternary complexes with UA and DAUA. Pd(II) also reacted with UA, DAUA, EUA, and N-substituted Delta(2,11)-enaminousnic acids to give the corresponding binary complexes. All the isolated complexes are insoluble in water and soluble in most organic solvents. They exhibited very strong absorption and circular dichroism spectral peaks in the UV region. The (1)H-NMR spectrum in CDCl(3) of the Pd(II) complex of N-phenyl-Delta(2,11)-enaminousnic acid (PEUA), Pd(PEUA)(2) x C(6)H(6), showed that the C(4)-proton signal suffered a large upfield shift (0.86 ppm) due to the ring current effect of the N-phenyl moiety. X-Ray crystal structure analysis has been performed for Cu(bpy)(UA)(ClO(4)) x CH(3)OH, Pd(MEUA)(2) x C(6)H(6), and Pd(PEUA)(2) x C(6)H(6). Cu(bpy)(UA)(ClO(4)) x CH(3)OH has a square-pyramidal structure with the two nitrogen atoms of bpy and the two oxygen atoms of the mono-deprotonated B ring of UA in the equatorial positions, while Pd(II) binds with two molecules of MEUA or PEUA in the trans configuration through the nitrogen and oxygen atoms with deprotonation. The N-phenyl ring of PEUA in Pd(PEUA)(2).C(6)H(6) was revealed to be located close to the C(4) proton as indicated by (1)H-NMR. Isolation of Cu(2)(bpy)(2)(UA)(NO(3))(2) x 2H(2)O suggests that UA has two metal binding sites that can form polymeric complexes. The present results substantiate the metal binding ability and the structures of the complexes of usnic acid and other substances from lichens as biomonitors of environmental metal ions.
采用合成和光谱方法研究了酚类地衣物质松萝酸(UA)及其乙酰基和烯胺衍生物9 - O - 乙酰松萝酸(MAUA)、7,9 - 二 - O - 乙酰松萝酸(DAUA)、Δ(2,11) - 烯胺松萝酸(EUA)以及N - 取代的Δ(2,11) - 烯胺松萝酸的金属配位性质,并通过X射线衍射法确定了铜(II)和钯(II)配合物的结构。Cu(II)与UA和DAUA反应分别生成二元配合物Cu(UA)₂·H₂O和Cu(DAUA)₂,并且Cu(bpy)(bpy = 2,2'-联吡啶)与UA和DAUA形成三元配合物。Pd(II)也与UA、DAUA、EUA以及N - 取代的Δ(2,11) - 烯胺松萝酸反应生成相应的二元配合物。所有分离得到的配合物均不溶于水,可溶于大多数有机溶剂。它们在紫外区域表现出很强的吸收和圆二色光谱峰。N - 苯基 - Δ(2,11) - 烯胺松萝酸(PEUA)的钯(II)配合物Pd(PEUA)₂·C₆H₆在CDCl₃中的¹H - NMR谱表明,由于N - 苯基部分的环电流效应,C(4) - 质子信号发生了很大的高场位移(0.86 ppm)。对Cu(bpy)(UA)(ClO₄)·CH₃OH、Pd(MEUA)₂·C₆H₆和Pd(PEUA)₂·C₆H₆进行了X射线晶体结构分析。Cu(bpy)(UA)(ClO₄)·CH₃OH具有四方锥结构,bpy的两个氮原子和单去质子化的UA的B环的两个氧原子位于赤道位置,而Pd(II)通过去质子化的氮原子和氧原子以反式构型与两个MEUA或PEUA分子结合。¹H - NMR表明,Pd(PEUA)₂·C₆H₆中PEUA的N - 苯基环靠近C(4)质子。Cu₂(bpy)₂(UA)(NO₃)₂·2H₂O的分离表明UA有两个金属结合位点,可以形成聚合物配合物。目前的结果证实了松萝酸和地衣中其他物质作为环境金属离子生物监测剂的金属配位能力和配合物结构。