Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands
碩士 === 國立彰化師範大學 === 化學系 === 104 === The substitution studies of dimeric Fe-S complex, [Fe2(OSC6H4)4]-2, toward several phenolate and phenothiolate ligands (C6H5O-, C6H5S-, HOC6H4S- and -OC6H5S-SC6H5O-) were presented in this report. In alkaline conditions, four new five-coordinated Fe-S complexes we...
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ndltd-TW-104NCUE50650012017-10-15T04:37:07Z http://ndltd.ncl.edu.tw/handle/54259313187606380670 Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands 鐵金屬錯合物 [K2][Fe2(1,2-OSC6H4)4] 與硫/氧配位基之反應與探討 施聖瑩 碩士 國立彰化師範大學 化學系 104 The substitution studies of dimeric Fe-S complex, [Fe2(OSC6H4)4]-2, toward several phenolate and phenothiolate ligands (C6H5O-, C6H5S-, HOC6H4S- and -OC6H5S-SC6H5O-) were presented in this report. In alkaline conditions, four new five-coordinated Fe-S complexes were generated with the separation of two moieties of [Fe(OSC6H4)2]- from starting dimeric Fe-S complex. The synthesized complexes were characterized by ESI-Mass, EPR and X-ray diffraction analyses. In addition, the roles of cation, especially K+, in the successful production of these complexes were investigated. Interestingly, we found that a monomeric six-coordinated Fe-S complex, [Fe(OSC6H4)3]-3, can be generated in the solution containing only the starting dimeric Fe-S complex in alkaline conditions. This complex were characterized by ESI-Mass, EPR, UV-vis and X-ray diffraction analyses. 洪義盛 2016 學位論文 ; thesis 92 zh-TW |
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碩士 === 國立彰化師範大學 === 化學系 === 104 === The substitution studies of dimeric Fe-S complex, [Fe2(OSC6H4)4]-2, toward several phenolate and phenothiolate ligands (C6H5O-, C6H5S-, HOC6H4S- and -OC6H5S-SC6H5O-) were presented in this report. In alkaline conditions, four new five-coordinated Fe-S complexes were generated with the separation of two moieties of [Fe(OSC6H4)2]- from starting dimeric Fe-S complex. The synthesized complexes were characterized by ESI-Mass, EPR and X-ray diffraction analyses. In addition, the roles of cation, especially K+, in the successful production of these complexes were investigated. Interestingly, we found that a monomeric six-coordinated Fe-S complex, [Fe(OSC6H4)3]-3, can be generated in the solution containing only the starting dimeric Fe-S complex in alkaline conditions. This complex were characterized by ESI-Mass, EPR, UV-vis and X-ray diffraction analyses.
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洪義盛 |
author_facet |
洪義盛 施聖瑩 |
author |
施聖瑩 |
spellingShingle |
施聖瑩 Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
author_sort |
施聖瑩 |
title |
Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
title_short |
Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
title_full |
Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
title_fullStr |
Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
title_full_unstemmed |
Reactivity Studies of [K2][Fe2(1,2-OSC6H4)4] with S/O-containing ligands |
title_sort |
reactivity studies of [k2][fe2(1,2-osc6h4)4] with s/o-containing ligands |
publishDate |
2016 |
url |
http://ndltd.ncl.edu.tw/handle/54259313187606380670 |
work_keys_str_mv |
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1718555178242670592 |