Single-Spin Magnetic Resonance in the Nitrogen-Vacancy Center of Diamond
Single-Spin Magnetic Resonance in the Nitrogen-Vacancy Center of Diamond
Publication date: Available online 26 December 2016
Source:Progress in Nuclear Magnetic Resonance Spectroscopy</br>
Author(s): Dieter Suter, Fedor Jelezko</br>
Magnetic resonance of single spins has flourished mostly because of the unique properties of the NV center in diamond. This review covers the basic physics of this defect center, introduces the techniques for working with single spins and gives an overview of some applications like quantum information and sensing.
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[Question from NMRWiki Q&A forum] spin lock 1H spectrum
spin lock 1H spectrum
Please, if somebody wants to help me?! I need to get 1H spectrum with spin lock pulse on Bruker AV 600 instrument. Which pulse sequence and which parameters should be used, please? Thank you, thank you, Marijana from Croatia
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09-22-2011 05:37 AM
[NMR paper] Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxi
Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxidized and reduced Escherichia coli thioredoxin.
Related Articles Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxidized and reduced Escherichia coli thioredoxin.
J Biomol NMR. 1994 May;4(3):411-32
Authors: Chandrasekhar K, Campbell AP, Jeng MF, Holmgren A, Dyson HJ
As a prelude to complete structure calculations of both the oxidized and reduced forms of Escherichia coli thioredoxin (M(r) 11,700), we have analyzed the NMR...
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08-22-2010 03:33 AM
[NMR paper] Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxi
Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxidized and reduced Escherichia coli thioredoxin.
Related Articles Effect of disulfide bridge formation on the NMR spectrum of a protein: studies on oxidized and reduced Escherichia coli thioredoxin.
J Biomol NMR. 1994 May;4(3):411-32
Authors: Chandrasekhar K, Campbell AP, Jeng MF, Holmgren A, Dyson HJ
As a prelude to complete structure calculations of both the oxidized and reduced forms of Escherichia coli thioredoxin (M(r) 11,700), we have analyzed the NMR...