Teleb S M, Refat M S
Chemistry Department, Faculty of Science, Zagazig University, Zagazig, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc. 2004 Jun;60(7):1579-86. doi: 10.1016/j.saa.2003.08.018.
The reaction of ferric(III) acetylacetonate (donor), Fe(acac)3, with iodine as a sigma-acceptor and with other different pi-acceptors have been studied spectrophotometrically at room temperature in chloroform. The pi-acceptors used in this investigation are 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), p-chloranil and 7,7',8,8'-tetracyanoquinodimethane (TCNQ). The results indicate the formation of 1:1 charge-transfer complexes with a general formula, [Fe(acac)3 (acceptors)]. The iodine complex was shown to contain the triiodide species, [Fe(acac)3]2I(+)I3-, based on the electronic absorptions as well as on the Far-infrared absorption bands characteristic for the non-linear triiodide species, I3-, with C2v symmetry. The proposed structure of this complex is further supported by thermal and middle infrared measurements.
在室温下于氯仿中,通过分光光度法研究了乙酰丙酮铁(III)(供体)Fe(acac)₃与作为σ受体的碘以及其他不同π受体的反应。本研究中使用的π受体为2,3 - 二氯 - 5,6 - 二氰基 - 1,4 - 苯醌(DDQ)、对苯醌氯和7,7',8,8' - 四氰基对苯二醌二甲烷(TCNQ)。结果表明形成了通式为[Fe(acac)₃(受体)]的1:1电荷转移配合物。基于电子吸收以及具有C₂ᵥ对称性的非线性三碘化物物种I₃⁻的特征远红外吸收带,碘配合物显示含有三碘化物物种[Fe(acac)₃]₂I⁺I₃⁻。该配合物的提议结构通过热测量和中红外测量得到进一步支持。