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Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands. / Su Jing

Swansea University Author: Su Jing

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The aim of this work was the synthesis of novel ferrocenyl chalcogenide ligands and their late transition metal complexes, and the study of relevant electrochemistry to provide information for exploring their potential application in a new type of electrochemical sensor. The introduction reviews fou...

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Published: 2006
Institution: Swansea University
Degree level: Doctoral
Degree name: Ph.D
URI: https://cronfa.swan.ac.uk/Record/cronfa42493
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spelling 2018-08-02T16:24:29.4469945 v2 42493 2018-08-02 Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands. 6b83ed3cd65efed018c91648ab65e4a3 NULL Su Jing Su Jing true true 2018-08-02 The aim of this work was the synthesis of novel ferrocenyl chalcogenide ligands and their late transition metal complexes, and the study of relevant electrochemistry to provide information for exploring their potential application in a new type of electrochemical sensor. The introduction reviews four sections of the literature. Group 6 metal carbonyl and palladium, platinum complexes of neutral chalcogenoether ligands are briefly introduced. The electrochemistry of linked ferrocenes is explored. Finally, the use of ferrocene in the design of electrochemical sensors is described. Subsequent chapters describe the synthesis and characterisation of novel ferrocenyl chalcogenide compounds, which can be divided into three categories: (1) Four series of ferrocenyl chalcogenide compounds with flexible saturated hydrocarbon chains: bidentate, linear tridentate, tripodal or tetradentate ligands; (2) Two macrocyclic ferrocenyl selenide compounds with four Se donor atoms; (3) Three ferrocenyl chalcogenide compounds with a rigid chain. Four compounds' structures have been determined by X-ray crystallography: FcSe(CH2)3SeFc, FcSe(CH2)3Se(CH2)3SeFc, difcSe4 and FcSeCH2C6H4CH2SeFc. The coordination chemistry of ferrocenyl chalcogenide compounds was then systematically studied. New compounds include: (1) Palladium and platinum complexes of the ligands with flexible saturated hydrocarbon chains; (2) Group 6 metal carbonyl complexes of bis(ferrocenylchalcogeno)propanes; (3) Palladium and platinum complexes of the macrocyclic ligands; (4) The platinum complex of FcSeCH2C6H4CH2SeFc. Techniques used to characterize these compounds include: multinuclear NMR spectroscopy; mass spectrometry; UV-vis and IR spectroscopy. Eighteen complexes' structures have been determined by X-ray crystallography: [M{lcub}FcE(CH2)3E'Fc{rcub}2](PF6)2 (M = Pd or Pt; E, E' = Se or Te), [MCl2(FcSeCH2SeFc)2] (M = Pd or Pt), [MCl2(FcTeCH2TeFc)] (M = Pd or Pt), [PdCl2(FcSeCH2CH2SeFc){rcub}, [PtCl {lcub}FcSe(CH2)3Se(CH2)3SeFc{rcub} ]PF6, [Cr(CO)4{lcub}FcTe(CH2)3TeFc{rcub}], [Mo(CO)4{lcub}FcE(CH2)3E'Fc{rcub}] (E, E' = Se or Te), [W(CO)4{lcub}FcTe(CH2)3TeFc{rcub}], and the supramolecular complex [Pt2Cl2{lcub}FcSeCH2C6H4CH2SeFc{rcub}3l(PF6)2 with an unusual dinuclear triple helical geometry. The electrochemistry study of the above compounds by cyclic voltammetry and differential pulse voltammetry proved that the communication between ferrocene units occurs via a through bond mechanism, and it is tentatively concluded that the interaction between ferrocene units can only happen when they occupy inequivalent positions. E-Thesis Organic chemistry. 31 12 2006 2006-12-31 COLLEGE NANME Chemistry COLLEGE CODE Swansea University Doctoral Ph.D 2018-08-02T16:24:29.4469945 2018-08-02T16:24:29.4469945 Faculty of Science and Engineering School of Engineering and Applied Sciences - Chemistry Su Jing NULL 1 0042493-02082018162458.pdf 10801723.pdf 2018-08-02T16:24:58.8370000 Output 30400548 application/pdf E-Thesis true 2018-08-02T16:24:58.8370000 false
title Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
spellingShingle Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
Su Jing
title_short Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
title_full Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
title_fullStr Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
title_full_unstemmed Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
title_sort Synthesis, complexation and electrochemistry of novel ferrocenyl chalcogenide ligands.
author_id_str_mv 6b83ed3cd65efed018c91648ab65e4a3
author_id_fullname_str_mv 6b83ed3cd65efed018c91648ab65e4a3_***_Su Jing
author Su Jing
author2 Su Jing
format E-Thesis
publishDate 2006
institution Swansea University
college_str Faculty of Science and Engineering
hierarchytype
hierarchy_top_id facultyofscienceandengineering
hierarchy_top_title Faculty of Science and Engineering
hierarchy_parent_id facultyofscienceandengineering
hierarchy_parent_title Faculty of Science and Engineering
department_str School of Engineering and Applied Sciences - Chemistry{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Chemistry
document_store_str 1
active_str 0
description The aim of this work was the synthesis of novel ferrocenyl chalcogenide ligands and their late transition metal complexes, and the study of relevant electrochemistry to provide information for exploring their potential application in a new type of electrochemical sensor. The introduction reviews four sections of the literature. Group 6 metal carbonyl and palladium, platinum complexes of neutral chalcogenoether ligands are briefly introduced. The electrochemistry of linked ferrocenes is explored. Finally, the use of ferrocene in the design of electrochemical sensors is described. Subsequent chapters describe the synthesis and characterisation of novel ferrocenyl chalcogenide compounds, which can be divided into three categories: (1) Four series of ferrocenyl chalcogenide compounds with flexible saturated hydrocarbon chains: bidentate, linear tridentate, tripodal or tetradentate ligands; (2) Two macrocyclic ferrocenyl selenide compounds with four Se donor atoms; (3) Three ferrocenyl chalcogenide compounds with a rigid chain. Four compounds' structures have been determined by X-ray crystallography: FcSe(CH2)3SeFc, FcSe(CH2)3Se(CH2)3SeFc, difcSe4 and FcSeCH2C6H4CH2SeFc. The coordination chemistry of ferrocenyl chalcogenide compounds was then systematically studied. New compounds include: (1) Palladium and platinum complexes of the ligands with flexible saturated hydrocarbon chains; (2) Group 6 metal carbonyl complexes of bis(ferrocenylchalcogeno)propanes; (3) Palladium and platinum complexes of the macrocyclic ligands; (4) The platinum complex of FcSeCH2C6H4CH2SeFc. Techniques used to characterize these compounds include: multinuclear NMR spectroscopy; mass spectrometry; UV-vis and IR spectroscopy. Eighteen complexes' structures have been determined by X-ray crystallography: [M{lcub}FcE(CH2)3E'Fc{rcub}2](PF6)2 (M = Pd or Pt; E, E' = Se or Te), [MCl2(FcSeCH2SeFc)2] (M = Pd or Pt), [MCl2(FcTeCH2TeFc)] (M = Pd or Pt), [PdCl2(FcSeCH2CH2SeFc){rcub}, [PtCl {lcub}FcSe(CH2)3Se(CH2)3SeFc{rcub} ]PF6, [Cr(CO)4{lcub}FcTe(CH2)3TeFc{rcub}], [Mo(CO)4{lcub}FcE(CH2)3E'Fc{rcub}] (E, E' = Se or Te), [W(CO)4{lcub}FcTe(CH2)3TeFc{rcub}], and the supramolecular complex [Pt2Cl2{lcub}FcSeCH2C6H4CH2SeFc{rcub}3l(PF6)2 with an unusual dinuclear triple helical geometry. The electrochemistry study of the above compounds by cyclic voltammetry and differential pulse voltammetry proved that the communication between ferrocene units occurs via a through bond mechanism, and it is tentatively concluded that the interaction between ferrocene units can only happen when they occupy inequivalent positions.
published_date 2006-12-31T03:53:04Z
_version_ 1763752631050698752
score 11.012678

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