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  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 化學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/2572
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dc.contributor.advisor劉緒宗(Shiuh-Tzung Liu)
dc.contributor.authorShu-Ting Yangen
dc.contributor.author楊舒庭zh_TW
dc.date.accessioned2021-05-13T06:42:18Z-
dc.date.available2017-06-12
dc.date.available2021-05-13T06:42:18Z-
dc.date.copyright2017-06-12
dc.date.issued2017
dc.date.submitted2017-03-08
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/2572-
dc.description.abstract本篇論文分別合成2,7-bis(2-pyridyl)-1,8-naphthyridine (bpnp) 和 5-phenyl-2,8-bis(2,2’-bipyridin-6-yl)-1,9,10-anthyridine (pbbpa) 作為多牙配位基,利用這些配體與鈀金屬進行錯合反應,探討所生成錯合物的結構和催化應用。多牙氮配位基 bpnp 與乙酸鈀在甲醇和三氟醋酸下反應生成 Pd2(bpnp)(TFA)3(OH) (9),pbbpa 與 Pd(MeCN)2Cl2 反應,合成出雙金屬錯合物。由於其溶解度不佳,使用六氟磷酸鉀置換陰離子,生成 [Pd2(pbbpa)Cl2](PF6)2 (11),以核磁共振光譜和質譜分析分別鑑定結構。
論文中比較 9 和 11 對於硝基還原反應之催化活性之差異。在先前的研究工作中發現 [Pd2(pbbpa)Cl2](PF6)2 (11) 經過少量的 NaBH3CN 活化後,能夠在氫氣下還原硝基苯衍生物,而Pd2(bpnp)(TFA)3(OH) (9) 則是可以作為催化劑直接在氫氣下進行該還原反應。另外,對此催化系統的應用範圍做了廣泛性測試,並藉由動力學和可能的反應中間體的實驗,解析此催化的反應機構。發現 9 的催化過程是遵循縮合路徑,由 N-苯基羥胺和亞硝基苯縮合成氧化偶氮苯後,藉由雙金屬的協助進行後續的還原得到苯胺;而 11 的催化過程則和單金屬錯合物 Pd(bpy)(TFA)2 相同,是直接將 N-苯基羥胺還原成產物。
zh_TW
dc.description.abstractThe use of bimetallic complexes as catalysts for the catalytic reactions has received much attraction due to the possible synergistic effect between the metal ions. In this study, a naphthyridine-based multidentate ligand 2,7-bis(2-pyridyl)-1,8-naphthyridine (bpnp) and an anthyridine-based ligand 5-phenyl-2,8-bis(2,2’-bipyridin-6-yl)-1,9,10-anthyridine (pbbpa) were synthesized. Coordination of bpnp with Pd(OAc)2 in a mixture of MeOH and trifluoroacetic acid yielded the dipalladium complex Pd2(bpnp)(TFA)3(OH) (9). Treatment of pbbpa with Pd(MeCN)2Cl2 followed by anion exchange resulted in the formation of [Pd2(pbbpa)Cl2](PF6)2 (11). The structures of both complexes were confirmed by 1H-, 13C-NMR and ESI-HRMS.
In a previous work, the resulting complex obtained from treatment of 11 with NaBH3CN was catalytically active toward the reduction of nitroarenes in the presence of H2. In this work, complex 9 showed a similar activity without any pre-treatment. Comparison of the catalytic activity between these complexes was revealed. This catalytic system is applicable for various nitroarenes. The possible reaction mechanism of this catalytic system is established by the kinetic studies and the reactivity of possible intermediates under the catalytic conditions. 9 catalyzed through the condensation pathway, in which N-phenylhydroxylamine and nitrosobenzene formed azoxybenzene, and gave aniline by following reduction with the assistance of dimetal complex. On the other hand, 11 and Pd(bpy)(TFA)2 catalyzed through direct pathway, in which aniline was obtained by reduction of N-phenylhydroxylamine.
en
dc.description.provenanceMade available in DSpace on 2021-05-13T06:42:18Z (GMT). No. of bitstreams: 1
ntu-106-R03223118-1.pdf: 6772391 bytes, checksum: 030c79ab345cb56cbada90b0aa3fa346 (MD5)
Previous issue date: 2017
en
dc.description.tableofcontents摘要 1
Abstract II
目錄 III
附圖目錄 V
附表目錄 VI
流程目錄 VII
第一章 緒論 1
1.1 萘啶類多牙基與其雙金屬錯合物 1
1.2 蒽啶類多牙基與其雙金屬錯合物 4
1.3 硝基苯還原反應 7
1.4 研究目的 9
第二章 雙鈀金屬錯合物之合成與鑑定 10
2.1 配位基之合成 10
2.2 雙鈀金屬錯合物之合成與鑑定 12
2.3 雙鈀金屬錯合物 9 之配位基置換 17
第三章 雙鈀金屬錯合物之催化應用 22
3.1 反應條件最佳化 22
3.2 反應應用範圍 26
3.3 芳基鹵化物之還原反應探討 27
3.4 反應機構探討和與其他鈀催化劑之比較 31
3.5 催化劑重複反應測試 39
第四章 結論 40
第五章 實驗部分 42
5.1 General part 42
5.2 Synthetic procedures and characterization of compounds 43
5.2.1 Synthesis of ligand and palladium(II) complexes 43
5.2.2 Reduction of Nitroarenes 57
5.2.3 Investigation of Reaction Intermediates and Mechanism 64
參考文獻 69
附錄一 73
dc.language.isozh-TW
dc.subject硝基苯還原反應zh_TW
dc.subject雙鈀錯合物zh_TW
dc.subject催化反應zh_TW
dc.subject多牙氮配體zh_TW
dc.subjectreduction of nitroarenesen
dc.subjectdipalladium complexesen
dc.subjectcatalytic reactionen
dc.subjectmultidentate ligandsen
dc.title多牙氮配位基及雙金屬鈀錯合物的合成與其催化應用zh_TW
dc.titleSynthesis and Catalytic Application of Dipalladium Complexes with Multidentate Ligandsen
dc.typeThesis
dc.date.schoolyear105-2
dc.description.degree碩士
dc.contributor.oralexamcommittee林英智(Ying-Chih Lin),邱靜雯(Ching-Wen Chiu)
dc.subject.keyword雙鈀錯合物,催化反應,多牙氮配體,硝基苯還原反應,zh_TW
dc.subject.keyworddipalladium complexes,catalytic reaction,multidentate ligands,reduction of nitroarenes,en
dc.relation.page114
dc.identifier.doi10.6342/NTU201700680
dc.rights.note同意授權(全球公開)
dc.date.accepted2017-03-08
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
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