贝塔转结构的键在D(2) O2中得到稳定
Younhee Cho1, Laura B Sagle, Satoshi Iimura
1Department of Chemistry, Texas A&M University, 3255 TAMU, College Station, Texas 77843, USA.
Journal of the American Chemical Society
|November 19, 2009
概括
弹性样多 (ELP) 的较低临界溶液温度 (LCST) 受水类型和二次结构的影响. 结合,而不是疏水性,驱动了ELP在重水 (D2O) 和轻水 (H2O) 中的崩.
科学领域:
- 生物化学 生化学
- 聚合物科学 聚合物科学
- 物理化学 物理化学
背景情况:
- 弹性类多 (ELP) 呈现较低的临界溶液温度 (LCST) 现象,这对于它们的刺激反应行为至关重要.
- 了解影响ELP阶段过渡的因素对于设计先进的生物材料和药物输送系统至关重要.
研究的目的:
- 调查ELP链长度和客残留化学物质在D2O和H2O中对LCST的影响.
- 为了将重水和轻水之间的LCST值差异与ELP链的二次结构形成联系起来.
主要方法:
- 在D2O和H2O中测量较低的临界溶液温度 (LCST).
- 循环二元化 (CD) 和红外 (IR) 光谱用于二次结构分析.
- 差异扫描热度计 (DSC) 用于热力学分析.
主要成果:
- 在D2O和H2O之间观察到LCST的显著差异,与二次结构相关.
- 形成更大的β-转/β-聚合结构的多体在H2O和D2O之间显示出更大的LCST转移.
- 这些特定的ELP被发现是最少的疏水性,表明疏水性的作用减少了.
结论:
- 与H2O相比,在D2O中稳定ELP的崩状态方面,结起的作用比疏水性更为关键.
- 二次结构形成,特别是β转和聚合物,是ELP对重水和轻水的差异反应的关键决定因素.
更多相关视频
10:28Probing the Structure and Dynamics of Interfacial Water with Scanning Tunneling Microscopy and Spectroscopy
Published on: May 27, 2018
11:27Studying Soft-matter and Biological Systems over a Wide Length-scale from Nanometer and Micrometer Sizes at the Small-angle Neutron Diffractometer KWS-2
Published on: December 8, 2016
相关概念视频
Hydrogen Bonds
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
Hydrogen Bonds
Hydrogen BondsHydrogen bonds are weak attractions between atoms that have formed other chemical bonds. One of these atoms is electronegative, like oxygen, and has a partial negative charge. The other is a hydrogen atom that has bonded with another electronegative atom and has a partial positive charge.Hydrogen Bonds Control the World!Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are...
Molecular Orbital Theory II
Molecular Orbital Energy Diagrams
Stability of Conjugated Dienes
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
¹H NMR of Labile Protons: Deuterium (²H) Substitution
This lesson illustrates the role of deuterium substitution in simplifying the NMR spectrum of compounds comprising labile protons. One method employed is the use of deuterium. Amongst the three isotopes of hydrogen, deuterium (2H) has a nucleus composed of one proton and one neutron. When the D2O solvent is added to a pure dry ethanol solution, its labile proton is substituted with deuterium.
π Molecular Orbitals of 1,3-Butadiene
Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, making them more stable. The enhanced stabilization of conjugated systems can be understood from their π molecular orbitals.
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
