Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas

碩士 === 國立交通大學 === 應用化學系碩博士班 === 99 === U-PBLG (uracil functional group tethered to poly(γ-benzyl-L-glutamate)) and MD-POSS (muti-diamidopyridine functionalized POSS) were synthesized via ring opening polymerization(ROP) and click reaction. The molecular recognition of U-PBLG/MD-POSS results in vario...

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Main Authors: Miao, Chia-Chun, 繆佳君
Other Authors: 張豐志
Format: Others
Language:zh-TW
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/96879768088018167256
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spelling ndltd-TW-099NCTU55000302016-08-22T04:17:26Z http://ndltd.ncl.edu.tw/handle/96879768088018167256 Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas 操控聚胜&;#32957;二級結構之超分子組裝於奈米層狀結構 Miao, Chia-Chun 繆佳君 碩士 國立交通大學 應用化學系碩博士班 99 U-PBLG (uracil functional group tethered to poly(γ-benzyl-L-glutamate)) and MD-POSS (muti-diamidopyridine functionalized POSS) were synthesized via ring opening polymerization(ROP) and click reaction. The molecular recognition of U-PBLG/MD-POSS results in various morphological changes. The association constant (Ka) for the complex, shows chemical shift of the amide proton of diamidopyridine in the complex U-PBLG/ MD-POSS was 114.07 M–1. The incorporation of MD-POSS into U-PBLG complex forms highly stable hydrogen-bonded complexes led to the red shift in CD spectra. The distance between the plane of hexagonally packed PBLG rods corresponding to d spacing of (31/2)q and 2q appeared in some blends to provide a driving force to form self-assemble into a thermodynamic stable of twisted macromolecular structures. U-PBLG/ MD-POSS blends complex that exhibited ordered cholesteric lamellar structures, with the d spacing being controlled by changing the U-PBLG content. 張豐志 2011 學位論文 ; thesis 119 zh-TW
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language zh-TW
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description 碩士 === 國立交通大學 === 應用化學系碩博士班 === 99 === U-PBLG (uracil functional group tethered to poly(γ-benzyl-L-glutamate)) and MD-POSS (muti-diamidopyridine functionalized POSS) were synthesized via ring opening polymerization(ROP) and click reaction. The molecular recognition of U-PBLG/MD-POSS results in various morphological changes. The association constant (Ka) for the complex, shows chemical shift of the amide proton of diamidopyridine in the complex U-PBLG/ MD-POSS was 114.07 M–1. The incorporation of MD-POSS into U-PBLG complex forms highly stable hydrogen-bonded complexes led to the red shift in CD spectra. The distance between the plane of hexagonally packed PBLG rods corresponding to d spacing of (31/2)q and 2q appeared in some blends to provide a driving force to form self-assemble into a thermodynamic stable of twisted macromolecular structures. U-PBLG/ MD-POSS blends complex that exhibited ordered cholesteric lamellar structures, with the d spacing being controlled by changing the U-PBLG content.
author2 張豐志
author_facet 張豐志
Miao, Chia-Chun
繆佳君
author Miao, Chia-Chun
繆佳君
spellingShingle Miao, Chia-Chun
繆佳君
Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
author_sort Miao, Chia-Chun
title Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
title_short Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
title_full Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
title_fullStr Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
title_full_unstemmed Supramolecular Assembly of Polypeptide Secondary Structures Confined in Nanolamellas
title_sort supramolecular assembly of polypeptide secondary structures confined in nanolamellas
publishDate 2011
url http://ndltd.ncl.edu.tw/handle/96879768088018167256
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