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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/123456789/62070
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor邱靜雯
dc.contributor.authorLi-Wei Chanen
dc.contributor.author詹立暐zh_TW
dc.date.accessioned2021-06-16T13:26:08Z-
dc.date.available2023-12-31
dc.date.copyright2013-07-30
dc.date.issued2013
dc.date.submitted2013-07-23
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/62070-
dc.description.abstract單芽氮異環碳烯之重元素相似物的性質及配位特性已經被研究了數十年,並
且在這方面有顯著的成果。然而,在單一分子中具有兩個以上的氮異環碳烯重元
素相似物卻是非常少見。因此,在本篇論文中,我們以合成具有高對稱性的多牙
氮異環碳烯重元素相似物為目標,其中包含了鍺烯、錫烯、r 及鉛烯,並對其做鑑
定及反應性的探討。在分子設計的部分,我們藉由立障極大的取代基,如:均三
甲苯和叔丁基,來穩定碳烯重元素相似物中的空軌域,並且以三亞苯作為分子骨
架來達成高對稱性分子的目的。鍺烯、錫烯、及鉛烯的合成,可以利用二價的鍺、
錫、鉛的前驅物,利用取代反應來獲得,並且以異核核磁共振光譜來證明其存在。
在矽烯的合成方面,我們先和成了四價的矽烷前驅物,之後再以強還原試劑將四
價矽還原成二價矽,但是在經過許多嘗試後,還是無法達到預期的結果。
zh_TW
dc.description.abstractBeing the heavier analogues of N-heterocyclic carbene, the coordination chemistry
of the so-called NHE (E = Si, Ge, Sn, Pb) have been investigated for decades. However,
while significant progresses were made in poly-NHCs, molecules bearing multiple NHE
units have only been reported few times. In this work, the syntheses of symmetrically
N,N’-substituted tritopic metallylenes featuring a rigid molecular backbone will be
presented. Tritopic NHSi precursors, dichlorosilanes, obtained from deprotonated
hexa-(alkylamino)triphenylene and SiCl4 failed in generating tri-silylene from chemical
reductions with K, KC8, and LiNp. On the other hand, reaction of deprotonated
hexamine and ECl2 (E = Sn, Pb) gives the desired tritopic metallylenes, which can also
be prepared from the reaction of hexamine and E[N(TMS)2]2 (E = Ge, Sn, Pb). The only
exception is the reaction of hexa-(tert-butylamino)triphenylene and Sn[N(TMS)2]2 that
yields the imine coordinated stannylene.
en
dc.description.provenanceMade available in DSpace on 2021-06-16T13:26:08Z (GMT). No. of bitstreams: 1
ntu-102-R00223116-1.pdf: 5528249 bytes, checksum: 294eb2e3fcb2006d0deceb3b9a9b0a5e (MD5)
Previous issue date: 2013
en
dc.description.tableofcontents口試委員會審定書 ............................................................................................................i
中文摘要 .......................................................................................................................... ii
ABSTRACT .................................................................................................................... iii
CONTENTS .....................................................................................................................iv
LIST OF FIGURES ..........................................................................................................vi
LIST OF SCHEMES ..................................................................................................... viii
Chapter 1 Introduction .............................................................................................. 1
1.1 Carbene ........................................................................................................... 1
1.2 Metallylenes .................................................................................................... 4
1.2.1 Silylene .................................................................................................. 4
1.2.2 Germylene ............................................................................................. 6
1.2.3 Stannylene ............................................................................................. 9
1.2.4 Plumbylene .......................................................................................... 11
1.3 Reactivity of Metallylenes ............................................................................ 13
1.4 Research Objective ....................................................................................... 15
Chapter 2 Molecular Design and Synthetic Methods ........................................... 18
2.1 Molecular Design.......................................................................................... 18
2.2 Synthetic Methods ........................................................................................ 20
Chapter 3 Results and Discussion ........................................................................... 23
3.1 Synthesis of Hexaminotriphenylenes ........................................................... 23
3.2 Synthesis of N-Heterocyclic Silylenes.......................................................... 24
3.3 Synthesis of N-Heterocyclic Germylenes ..................................................... 26
3.4 Synthesis of N-Heterocyclic Stannylenes ..................................................... 28
v
3.5 Synthesis of N-Heterocyclic Plumbylenes.................................................... 32
3.6 UV-Vis Spectrum of N-Heterocyclic Metallylenes ...................................... 35
3.7 Reactivities of N-Heterocyclic Metallylenes ................................................ 36
Chapter 4 Conclusions ............................................................................................. 38
Chapter 5 Experimental Section ............................................................................. 39
REFERENCES ................................................................................................................ 50
APPENDIX…………………………………………………………………………….54
dc.language.isoen
dc.title三芽氮異環碳烯之重元素相似物的合成與鑑定zh_TW
dc.titleSyntheses of Tritopic N-Heterocyclic Metallylenesen
dc.typeThesis
dc.date.schoolyear101-2
dc.description.degree碩士
dc.contributor.oralexamcommittee詹益慈,王志傑
dc.subject.keyword矽烯,鍺烯,錫烯,鉛烯,均三甲苯,叔丁基,三亞苯,zh_TW
dc.subject.keywordmetallylene,silylene,germylene,stannylene,plumbylene,en
dc.relation.page104
dc.rights.note有償授權
dc.date.accepted2013-07-23
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
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