1H NMR analysis of mixtures using internal standards: A quantitative experiment for the instrumental analysis laboratory

1992 ◽  
Vol 69 (10) ◽  
pp. 843 ◽  
Author(s):  
Jim Peterson
2012 ◽  
Vol 66 (5) ◽  
pp. 1000-1006 ◽  
Author(s):  
Elisabeth Linton ◽  
Asif Rahman ◽  
Sridhar Viamajala ◽  
Ronald C. Sims ◽  
Charles D. Miller

In this study, a proton nuclear magnetic resonance (1H NMR) method was developed to quantitatively analyze polyhydroxyalkanoate (PHA) content in Cupriavidus necator H16, Azotobacter vinelandii AvOP, and mixed microbial cultures from the effluent of an agricultural waste treatment anaerobic digester. In contrast to previous methods, a single-step PHA extractive method using deuterated chloroform was established, thereby facilitating direct 1H NMR analysis. The accuracy of the method was verified through comparison with well-established gas chromatography (GC) methanolysis techniques. Nile blue fluorescence staining was also carried out to serve as an independent and qualitative indicator of intracellular PHA content. The results indicate that the 1H NMR method is appropriate for rapid and non-destructive quantification of overall PHA content and determination of PHA copolymer composition in a variety of cultures. Notably, this technique was effective in measuring PHA content in full-strength waste samples where high concentrations of background impurities and organic compounds are present. The straightforward procedures minimize error-introducing steps, require less time and materials, and result in an accurate method suitable for routine analyses.


2015 ◽  
Vol 68 (12) ◽  
pp. 1810 ◽  
Author(s):  
Andrew S. Eastabrook ◽  
Jonathan Sperry

Readily available 3-substituted indoles undergo a one-pot iridium-catalyzed triborylation at the C2, C5, and C7 sites. 1H NMR analysis indicates borylation at C2 and C7 occurs first (no monoborylated product is observed), with the third borylation occurring as a separate, distinct step that is sterically directed to C5 by a combination of the substituent at C3 and the boronate at C7. The resulting tetrasubstituted indoles possess a substitution pattern that is cumbersome to prepare using existing methods.


FEBS Letters ◽  
1986 ◽  
Vol 209 (2) ◽  
pp. 265-268 ◽  
Author(s):  
Satoshi Koyama ◽  
Hiromi Daiyasu ◽  
Sumihiro Hase ◽  
Yuji Kobayashu ◽  
Yoshimasa Kyogoki ◽  
...  
Keyword(s):  
1H Nmr ◽  

Chemosphere ◽  
2008 ◽  
Vol 73 (1) ◽  
pp. S44-S52 ◽  
Author(s):  
Ana-Maria Geller ◽  
Heinz-Ulrich Krüger ◽  
Qing Liu ◽  
Cornelius Zetzsch ◽  
Manfred Elend ◽  
...  

2003 ◽  
Vol 60 (4) ◽  
pp. 186-191
Author(s):  
Hironori MATSUDA ◽  
Shizuo YAMASAKI ◽  
Tetsuo ASAKURA

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