9 research outputs found
Tetraphenylsilane๊ธฐ๋ฅผ ํฌํจํ์ฌ ์ฉ์ก ๊ณต์ ์ด ๊ฐ๋ฅํ ๊ณ ํจ์จ ์ธ๊ด ์ ๊ธฐ์ ๊ณ๋ฐ๊ด์์ ๋จ๋ถ์ ํธ์คํธ ๋ฌผ์ง์ ๊ดํ ์ฐ๊ตฌ
ํ์๋
ผ๋ฌธ (์์ฌ)-- ์์ธ๋ํ๊ต ๋ํ์ : ์ฌ๋ฃ๊ณตํ๋ถ, 2012. 8. ๋ฐ์์.๋ณธ ๋
ผ๋ฌธ์์๋ ๊ณ ํจ์จ์ ์ธ๊ด ์ ๊ธฐ์ ๊ณ๋ฐ๊ด์์๋ฅผ ๋ชฉํ๋ก ํ์ฌ, ํ
ํธ๋ผํ๋์ค๋ (Tetraphenylsilane) ๊ธฐ๋ฅผ ํฌํจํจ์ผ๋ก์จ ์ฉ์ก ๊ณต์ ์ด ๊ฐ๋ฅํด์ง๋ ์๋ก์ด ๋จ๋ถ์ ํธ์คํธ ๋ฌผ์ง๊ตฐ์ ๋ณด๊ณ ํ์๋ค. ์๋ก์ด ๊ฐ๋ฐ๋ ์ด ๋ฌผ์ง๊ตฐ์ TPS series ๋ผ ๋ช
๋ช
๋์์ผ๋ฉฐ, 9-phenyl-3-(4-(triphenylsilyl)phenyl)-carbazole (TPSPCz), 9-phenyl-3,6-bis(4-(triphenylsilyl)phenyl)-carbazole (TPS2PCz), 1,2-trans-bis(3,6-bis(4-(triphenylsilyl)phenyl)-carbazol-9-yl)cyclobutane (TPS4DCz) ๋ฑ ์ธ ๋ฌผ์ง๋ก ๊ตฌ์ฑ๋์ด ์๋ค. ์นด๋ฐ์กธ์ C3, C6 ์์น์ ์์ ๋์ ํ
ํธ๋ผํ๋์ค๋๊ธฐ๊ฐ ์นํ๋จ์ผ๋ก์จ ์ฉ์ก ๊ณต์ ์ ํตํด ๊ท ์ผํ ํ๋ฆ์ ์ป๋ ๊ฒ์ด ๊ฐ๋ฅํด์ก๋ค. ๋ํ ๊ด๋ฌผ๋ฆฌ์ , ํ๋ฆ์ ํํํ์ ํน์ฑ ์ฐ๊ตฌ์ ๊ธฐ์ดํ์ฌ, ๋ถํผ๊ฐ ํฌ๊ณ ์๋นํ ๋คํ๋ ค ์๋ ํํ์ ํ
ํธ๋ผํ๋์ค๋๊ธฐ๊ฐ ๊ฐ์ง๋ ๊ณต๊ฐ์ ๋ถ๋ฆฌ ํจ๊ณผ์ ์ํ์ฌ ๋์ผ ํ๋ฉด์์ ์์นํ๋ ์นด๋ฐ์กธ์ ์์๋จธ ํ์ฑ์ด ํจ๊ณผ์ ์ผ๋ก ์ต์ ๋๋ค๋ ๊ฒ์ ์ฆ๋ช
ํ์๋ค. ์ ํธ์คํธ ๋ฌผ์ง๋ค์ ํ
ํธ๋ผํ๋์ค๋๊ธฐ์ ์๊ฐ ์ฆ๊ฐํ ์๋ก ๋์ฑ ๋์ ์ด๋ถํด ์จ๋(์ ์ฒด ๋ฌด๊ฒ ์ค ์ฝ 5%์ ๋ฌด๊ฒ๊ฐ ์ค์ด๋๋ ์จ๋)๋ฅผ ๊ฐ๋ ํ์์ ๋ณด์๋ค (TPSPCz : 363 ยฐC, TPS2PCz : 424 ยฐC, TPS4DCz : 472 ยฐC). ํนํ fac-tris(2-phenylpyridine) iridium (III) (Ir(PPy)3) ๊ฐ ๊ฒ์คํธ, TPS4DCz๊ฐ ํธ์คํธ๋ก ์ฐ์ธ ์ธ๊ด ์ ๊ธฐ์ ๊ณ๋ฐ๊ด์์์ ๊ฒฝ์ฐ, Ir(PPy)3 ๊ฐ ๊ฒ์คํธ, PVK ๊ฐ ํธ์คํธ๋ก ์ฐ์ธ ์ธ๊ด ์ ๊ธฐ์ ๊ณ๋ฐ๊ด์์์ ๋น๊ตํ์์ ๋ ์ต๋ 154 % ๊น์ง ํฅ์๋ ์์ ์ฑ๋ฅ์ ๋ณด์ฌ์ฃผ์๋ค.ABSTRACT i
TABLE OF CONTENTS iii
LIST OF FIGURES v
LIST OF SCHEMES viii
LIST OF TABLES ix
CHAPTER I. Introduction 1
I-1. Physics of Electrophosphorescence 1
I-2. Physics of Electrophosphorescent Light-Emitting Devices 4
I-3. Recent Progress on Solution-Processable Host Materials for Electrophosphorescent Light-Emitting Devices 9
I-4. References 13
CHAPTER II. Tetraphenylsilane Containing Solution-Processable Small-Molecular Hosts for Highly Efficient Phosphorescent Organic Light-Emitting Diodes 15
II-1. Introduction 15
II-2. Results and Discussion 19
II-3. Conclusion 41
II-4. Experimental 42
II-5. References 50
ABSTRACT IN KOREAN 55
LIST OF PRESENTATIONS 57Maste
Egocentric groups characteristics of personality and adaptation aspects according to approach and avoid motivation
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ผ๋ฌธ(์์ฌ) --์์ธ๋ํ๊ต ๋ํ์ :์ฌ๋ฆฌํ๊ณผ,2009.2.Maste
The Formation of European Security Community: The Possiblity and Its Limits
This is a study on the possibility of the formation of the so-called European Security community and its limits. The Idea of the European integration movement was advocated by Jean Monnet for European economic development and the maintaining of peace in Europe immedately after WWII. In the same logic, Western European countries have successfully integrated into Euroepan Economic Community, but military-security perspective, they have long confronted through NATO and Warsaw Treaty Organizaion. The former is the allied institution on which western European countries depended their national defense and security and the later is the socialist alliance through which the old USSR and eastern European countries had pursued their national security.
Following the collapse of the old USSR and the democratization of eastern European countries, a new European international political environment and political order have emerged. First of all, Germany was reunified. CSCE has played a significant role in ending the era of the cold war which has been maintained for almost 45 years since WWII, and has emerged as the pan-European security community for the security and peace of the entire Europe. Through the conclusion of the Maastricht Treaty of 1991, the member-states of EC have agreed upon the establishment of the United States of Europe by means of economic, political, and diplomatic-defense integration. They thought such a European political union would function as a common European defense system. However, each member-states of EC has different interests and different attitudes toward the formation of a common European security community as well as the roles and functions of WEU and NATO. The Unites States considers yet NATO will be an appropriate institution, if it expands its economic and political roles rather than the military role, even in the era of the post-cold war and international peace and cooperations.
Generally speaking, it is a great advantage that CSCE has encompassed all the countries of western and eastern Europe, whereas its weakness is the lack of forcible means as a collective security system. WEU may be meaningful in that it is europeanized and will function as an European. security system, but it has limits in playing the role of the entire European security system. Although NATO has a strong organization and military power, but since it is the by-product of Cold War the expansion of influence of NATO following the collapse of the old USSR and the socialist camp will be misunderstood as that of the United States.
In conclusion, therefore, it is a best alternative that by encouraging the advantageous points of CSCE, WEU, and NATO and complementing each weakness of others, these organizations .pursue the cooperation in the European security and peace
๊ณต์ ์ฌ์ฐ์ ์ ๊ทน์ ๊ด๋ฆฌ๋ฐฉ์์ ๊ดํ ์ฐ๊ตฌ
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ผ๋ฌธ(์์ฌ)--์์ธ๋ํ๊ต ํ๊ฒฝ๋ํ์ :ํ๊ฒฝ๊ณํํ๊ณผ ๋์๋ฐ์ง์ญ๊ณํ์ ๊ณต,1996.Maste
์์ ์กฐ์ RNA์ ๋ฐ์ด๋ฌ์ค RNA์ ์์ฉํ๋ ๋จ๋ฐฑ์ง ๊ธฐ์์ ๊ดํ ๋จ์ผ ๋ถ์ ํ๊ด ์ฐ๊ตฌ
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ผ๋ฌธ(๋ฐ์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :์์ฐ๊ณผํ๋ํ ๋ฌผ๋ฆฌยท์ฒ๋ฌธํ๋ถ,2015. 8. ํ์ฑ์ฒ .Andrew Fire found that a specific gene was shut down with the destruction of messenger RNA (mRNA) when tiny snippets of double-stranded RNA (dsRNA) were injected into Caenorhabditis elegans in 1998. This phenomenon was RNA interference (RNAi), a biological process in the control of global gene expression, and it became one of most momentous biomedical discoveries of the last 30 years. The application of RNAi has revolutionized the studies of eukaryotic gene function in research laboratories, and the therapeutic potential for human disease treatment was also had captured the attention of the biological and medical communities. RNAi-based therapeutics were introduced into the clinical trials just six years after the discovery. Because components of the RNAi machinery are to be regulated extensively, it became a major challenge to understand their molecular mechanisms from the biogenesis to effective pathways.
MicroRNAs (miRNAs) are ~22nt nucleotide endogenous RNAs central to RNAi with small interfering RNA (siRNA). RNA transcripts are process by Microprocessors in nucleus to be precursors of miRNAs. We observed the procedure that complexes of recombinant Drosha and DiGeorge syndrome chromosomal region 8 (DGCR8) fused to fluorescence proteins bind on hairpin structured primary miRNA at single-molecule level, and showed that a Microprocessor is composed of one Drosha molecule and two DGCR8 molecules. This stoichiometry issue was remained ambiguous due to the heterogeneous behaviors of Microprocessor components in the previous biochemical studies, but it could be clarified with real-time single-molecular observation.
Argonaute proteins are highly conserved central effectors of RNAi among eukaryotes. The processed miRNAs incorporate with Argonaute proteins into the RNA-induced silencing complexes (RISCs), and the RISCs search and act on targets by miRNA sequence complementary. We observed target binding procedures of core-RISCs followed by target cleavage, guide RNA unloading, and stable binding pathways at single-molecule level with recombinant human Argonuate 2 and organic dye labeled RNA substrates. The whole procedure of core-RISC reaction was described with kinetic parameters at each stage including core-RISC recycling. Furthermore, we discovered the stable binding mode of core-RISC and RNA sequence dependency on core-RISC pathway providing a clue for improving siRNA design.
Some viruses store their genetic information as long double stranded RNAs (dsRNAs), and they insert the RNA molecules into normal cells for infection. The normal cells should distinguish the exogenous RNAs from their endogenous RNAs and activate an immune system to survive, and one of the strategies is to measure the length of RNA molecules. Because normal cells do not have long dsRNA molecules, viral RNA invasion can be noticed if cells can discriminate the long dsRNA (> 1 kb) molecules. Previous cell studies showed that Melanoma Differentiation-Associated protein 5 (MDA5) would be essential for the process. By observing the formation and disassembling procedure of MDA5 filament on dsRNA in real-time at single-molecule level with an organic dye labeled recombinant MDA5 and dsRNAs, we explained the mechanism how small MDA5s can determine the length of dsRNA more than 100 times longer than them.Abstract
Contents
List of Figures and Tables
Chapter 1 Introduction
1.1. Single-Molecule Fluorescence Spectroscopy
1.2. TIRF Microscopy for Single-Molecule FRET Measurement
1.3. RNA Biology
References
Chapter 2 Stoichiometry of DROSHA-DGCR8 Complex
2.1. Introduction
2.2. Materials and Methods
2.3. Results and Discussion
2.4. Conclusion and Outlook
References
Chapter 3 Diverse Reaction pathways of Human Argonaute 2 on target RNAs
3.1. Introduction
3.2. Materials and Methods
3.3. Results and Discussion
3.4. Conclusion and Outlook
References
Chapter 4 RNA Length Discrimination Mechanism by MDA5 Filaments
4.1. Introduction
4.2. Materials and Methods
4.3. Results and Discussion
4.4. Conclusion and Outlook
References
Abstract in Korean (๊ตญ๋ฌธ์ด๋ก)
Publication List
Acknowledgement (๊ฐ์ฌ์ ๊ธ)Docto