Metal binding sites and partial structures of soil fulvic and humic acids compared: Aided by Eu(III) luminescence spectroscopy and DEPT/QUAT C-13 NMR pulse techniques
被引:22
作者:
Shin, HS
论文数: 0引用数: 0
h-index: 0
机构:Department of Chemistry, Korea Adv. Inst. of Sci./Technology, Taejon 305-701
Shin, HS
Rhee, SW
论文数: 0引用数: 0
h-index: 0
机构:Department of Chemistry, Korea Adv. Inst. of Sci./Technology, Taejon 305-701
Rhee, SW
Lee, BH
论文数: 0引用数: 0
h-index: 0
机构:Department of Chemistry, Korea Adv. Inst. of Sci./Technology, Taejon 305-701
Lee, BH
Moon, CH
论文数: 0引用数: 0
h-index: 0
机构:Department of Chemistry, Korea Adv. Inst. of Sci./Technology, Taejon 305-701
Moon, CH
机构:
[1] Department of Chemistry, Korea Adv. Inst. of Sci./Technology, Taejon 305-701
The excitation spectra (F-7(o)-->D-5(o) transition) of Eu(III)-fulvate and -humate were analyzed by a Lorentzian-Gaussian curve fitting method, and they revealed the formation of 1:1 (EuL(2+); L=carboxylate: similar to 579.04 nm) and 1:2 (EuL(2)(+): similar to 579.25 nm) complexes. This suggested that soil fulvic and humic acids have metal binding sites in two different chemical environments made up of carboxylate moieties. However, the 1:2 complex (EuL(2)(+)) seemed to be preponderant in fulvic acid rather than humic acid. This may be caused by the differences in their partial structures and functional group contents. The differences between soil fulvic and humic acids are discussed with the aid of the C-13 NMR DEFT (distortionless enhancement by polarization transfer pulse sequence) and QUAT (quaternary carbon only spectral subspectra. Copyright (C) 1996 Elsevier Science Ltd.