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金上二茂铁酰基β-肽单层的电化学。

Electrochemistry of ferrocenoyl beta-peptide monolayers on gold.

机构信息

MacDiarmid Institute for Advanced Materials and Nanotechnology, Department of Chemistry, University of Canterbury, Private Bag 4800, Christchurch, New Zealand.

出版信息

Langmuir. 2010 Jan 19;26(2):1334-9. doi: 10.1021/la902402t.

Abstract

The electrochemistry of self-assembled monolayers (SAMs) on gold containing a lipoic acid linker, the beta-peptide sequence (beta(3)Val-beta(3)Ala-beta(3)Leu)(n) for n = 1, 2, and a terminal ferrocenyl group has been described for the first time. Circular dichroism (CD), NMR, and molecular modeling were used to evaluate the beta-peptide structure in solution, while the monolayer film organization and electron-transfer kinetics were evaluated by cyclic voltammetry, chronoamperometry (CA), and ellipsometry. The peptides were assembled from trifluoroethanol solutions, where they are linear (n = 1) or helical (n = 2) based on CD, NMR, ellipsometry, and modeling evidence. The structure of the SAMs is less well understood. There is evidence for noncompact layers that allow electrolyte ions to approach the interface. Electron-transfer rates for n = 1, 2 were found to be 2500 and 1200 s(-1), respectively, and CA evidence indicated that the transfer is based on the hopping mechanism.

摘要

首次描述了含硫辛酸连接体的金上自组装单层(SAM)的电化学,β-肽序列(β(3)Val-β(3)Ala-β(3)Leu)(n),n = 1、2 和末端二茂铁基。圆二色性(CD)、NMR 和分子建模用于评估溶液中β-肽的结构,而通过循环伏安法、计时安培法(CA)和椭圆偏振法评估单层膜组织和电子转移动力学。肽是从三氟乙醇溶液中组装的,根据 CD、NMR、椭圆偏振和建模证据,它们在溶液中是线性的(n = 1)或螺旋的(n = 2)。SAM 的结构不太清楚。有证据表明非紧凑层允许电解质离子接近界面。n = 1、2 的电子转移速率分别为 2500 和 1200 s(-1),CA 证据表明转移基于跳跃机制。

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