Patel R N, Singh Nripendra, Shukla K K, Gundla V L N
Department of Chemistry, A.P.S. University, Rewa, M.P. 486003, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2005 Jun;61(8):1893-7. doi: 10.1016/j.saa.2004.07.019.
X-band E.S.R., magnetic and electronic spectra of some imidazolate-bridged homometallic complexes (en)2Cu-R-Im-Cu(en)23 where en, ethylenediamine; R-ImH, R = H imidazole (ImH); if R = CH3, 2-methylimidazole (M-ImH) and if R = C2H5, 2-ethylimidazole (E-ImH), and mononuclear complexes (en)Cu-dien2 and (en)Cu-PMDT2 where dien, diethylenetriamine; PMDT, pentamethyldiethylenetriamine have been described. Superoxide dismutase (SOD) activity has also been measured and compared with earlier reported complexes. In frozen solution at 77 K, the spectra show axial symmetry with a d(x2-y2) ground state. Difference in lambda(max) between mononuclear and binuclear complexes was found to be approximately 65-75 nm. Magnetic susceptibility and E.S.R. spectral measurements for all these binuclear complexes revealed that the copper(II) ions are involved in antiferromagnetic exchange interactions propagated by the imidazolate bridge.
一些咪唑桥连同金属配合物(en)₂Cu-R-Im-Cu(en)₂₃(其中en为乙二胺;R-ImH,R = H时为咪唑(ImH);R = CH₃时为2-甲基咪唑(M-ImH);R = C₂H₅时为2-乙基咪唑(E-ImH))以及单核配合物(en)Cu-dien₂和(en)Cu-PMDT₂(其中dien为二乙烯三胺;PMDT为五甲基二乙烯三胺)的X波段电子自旋共振(E.S.R.)、磁性和电子光谱已被描述。还测定了超氧化物歧化酶(SOD)活性,并与早期报道的配合物进行了比较。在77K的冷冻溶液中,光谱显示出具有d(x² - y²)基态的轴向对称性。发现单核和双核配合物之间的λ(max)差异约为65 - 75nm。所有这些双核配合物的磁化率和E.S.R.光谱测量表明,铜(II)离子参与了由咪唑桥传递的反铁磁交换相互作用。