Synthesis and NMR analysis of 13C and 15N-labeled long-chain polyamines (LCPAs)

被引:4
|
作者
Abacilar, Maryna [1 ]
Daus, Fabian [1 ]
Haas, Christian [1 ]
Brueckner, Stephan Ingmar [2 ]
Brunner, Eike [2 ]
Geyer, Armin [1 ]
机构
[1] Univ Marburg, Fachbereich Chem, Hans Meerwein Str 4, D-35032 Marburg, Germany
[2] Tech Univ Dresden, Fachrichtung Chem & Lebensmittelchem, D-01062 Dresden, Germany
来源
RSC ADVANCES | 2016年 / 6卷 / 96期
关键词
SILICA NANOSPHERES; DIATOM BIOSILICA; SPECTROSCOPY; REDUCTION; RESONANCE; CLEAVAGE; MILD;
D O I
10.1039/c6ra19624a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N-15, C-13, or both isotope labels were introduced in selected positions of several LCPAs containing 5, 11, or 13 nitrogens. The number of transformations during chemical synthesis wasminimized by coupling Fmoc-glycine-N-15, Fmoc-glycine-1-C-13, or Fmoc-beta-alanine simultaneously at both ends of the growing oligoamide chain on resin-linked norspermidine. LCPAs containing 10-20 nitrogens are the main organic constituent of diatom biosilica. Preliminary NMR studies of bioinspired silica nanocomposites obtained from double-labeled LCPA 14 and Si-29-enriched orthosilicic acid identified the close spatial arrangement of Si-29 and C-13 nuclei.
引用
收藏
页码:93343 / 93348
页数:6
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