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采用 Fmoc-甘氨酸测定核壳材料中结合的 Fmoc 基团的浓度的有效方法。

Efficient Method for the Concentration Determination of Fmoc Groups Incorporated in the Core-Shell Materials by Fmoc-Glycine.

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Gdansk, Wita Stwosza 63, 80-308 Gdansk, Poland.

Corrosion and Materials Engineering, Department of Electrochemistry, Faculty of Chemistry, Gdansk University of Technology, Narutowicza 11/12, 80-233 Gdansk, Poland.

出版信息

Molecules. 2020 Sep 1;25(17):3983. doi: 10.3390/molecules25173983.

Abstract

In this paper, we described the synthesis procedure of TiO@SiO core-shell modified with 3-(aminopropyl)trimethoxysilane (APTMS). The chemical attachment of Fmoc-glycine (Fmoc-Gly-OH) at the surface of the core-shell structure was performed to determine the amount of active amino groups on the basis of the amount of Fmoc group calculation. We characterized nanostructures using various methods: transmission electron microscope (TEM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) to confirm the modification effectiveness. The ultraviolet-visible spectroscopy (UV-vis) measurement was adopted for the quantitative determination of amino groups present on the TiO@SiO core-shell surface by determination of Fmoc substitution. The nanomaterials were functionalized by Fmoc-Gly-OH and then the fluorenylmethyloxycarbonyl (Fmoc) group was cleaved using 20% () solution of piperidine in DMF. This reaction led to the formation of a dibenzofulvene-piperidine adduct enabling the estimation of free Fmoc groups by measurement the maximum absorption at 289 and 301 nm using UV-vis spectroscopy. The calculations of Fmoc loading on core-shell materials was performed using different molar absorption coefficient: 5800 and 6089 dm × mol × cm for λ = 289 nm and both 7800 and 8021 dm × mol × cm for λ = 301 nm. The obtained results indicate that amount of Fmoc groups present on TiO@SiO-(CH)-NH was calculated at 6 to 9 µmol/g. Furthermore, all measurements were compared with Fmoc-Gly-OH used as the model sample.

摘要

本文描述了用 3-(氨丙基)三甲氧基硅烷(APTMS)对 TiO@SiO 核壳进行改性的合成过程。通过 Fmoc 基团计算来确定活性氨基的数量,在核壳结构表面进行 Fmoc-甘氨酸(Fmoc-Gly-OH)的化学连接。我们使用各种方法对纳米结构进行了表征:透射电子显微镜(TEM)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、热重分析(TGA)和 X 射线光电子能谱(XPS),以确认修饰效果。通过测定 Fmoc 取代来采用紫外可见光谱(UV-vis)测量定量确定存在于 TiO@SiO 核壳表面的氨基数量。通过 Fmoc-Gly-OH 对纳米材料进行功能化,然后使用 DMF 中的 20%()哌啶溶液裂解氟芴甲氧羰基(Fmoc)基团。该反应导致二苯并呋喃-哌啶加合物的形成,通过使用 UV-vis 光谱测量在 289 和 301nm 处的最大吸收来估计游离 Fmoc 基团。使用不同的摩尔消光系数对核壳材料上的 Fmoc 负载进行了计算:对于 λ=289nm,分别为 5800 和 6089dm×mol×cm;对于 λ=301nm,均为 7800 和 8021dm×mol×cm。得到的结果表明,TiO@SiO-(CH)-NH 上存在的 Fmoc 基团数量计算为 6 至 9µmol/g。此外,所有测量均与用作模型样品的 Fmoc-Gly-OH 进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5185/7504793/d2295b54beaf/molecules-25-03983-g001.jpg

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