Literature DB >> 29501956

Verdazyl-ribose: A new radical for solid-state dynamic nuclear polarization at high magnetic field.

Kent R Thurber1, Thanh-Ngoc Le2, Victor Changcoco2, David J R Brook2.   

Abstract

Solid-state dynamic nuclear polarization (DNP) using the cross-effect relies on radical pairs whose electron spin resonance (ESR) frequencies differ by the nuclear magnetic resonance (NMR) frequency. We measure the DNP provided by a new water-soluble verdazyl radical, verdazyl-ribose, under both magic-angle spinning (MAS) and static sample conditions at 9.4 T, and compare it to a nitroxide radical, 4-hydroxy-TEMPO. We find that verdazyl-ribose is an effective radical for cross-effect DNP, with the best relative results for a non-spinning sample. Under non-spinning conditions, verdazyl-ribose provides roughly 2× larger 13C cross-polarized (CP) NMR signal than the nitroxide, with similar polarization buildup times, at both 29 K and 76 K. With MAS at 7 kHz and 1.5 W microwave power, the verdazyl-ribose does not provide as much DNP as the nitroxide, with the verdazyl providing less NMR signal and a longer polarization buildup time. When the microwave power is decreased to 30 mW with 5 kHz MAS, the two types of radical are comparable, with the verdazyl-doped sample having a larger NMR signal which compensates for its longer polarization buildup time. We also present electron spin relaxation measurements at Q-band (1.2 T) and ESR lineshapes at 1.2 and 9.4 T. Most notably, the verdazyl radical has a longer T1e than the nitroxide (9.9 ms and 1.3 ms, respectively, at 50 K and 1.2 T). The verdazyl electron spin lineshape is significantly affected by the hyperfine coupling to four 14N nuclei, even at 9.4 T. We also describe 3000-spin calculations to illustrate the DNP potential of possible radical pairs: verdazyl-verdazyl, verdazyl-nitroxide, or nitroxide-nitroxide pairs. These calculations suggest that the verdazyl radical at 9.4 T has a narrower linewidth than optimal for cross-effect DNP using verdazyl-verdazyl pairs. Because of the hyperfine coupling contribution to the electron spin linewidth, this implies that DNP using the verdazyl radical would improve at lower magnetic field. Another conclusion from the calculations is that a verdazyl-nitroxide bi-radical would be expected to be slightly better for cross-effect DNP than the nitroxide-nitroxide bi-radicals commonly used now, assuming the same spin-spin coupling constants. Published by Elsevier Inc.

Entities:  

Keywords:  Cross-effect mechanism; Dynamic nuclear polarization; Magic-angle spinning; Radical; Solid state NMR; Verdazyl

Mesh:

Substances:

Year:  2018        PMID: 29501956      PMCID: PMC5856651          DOI: 10.1016/j.jmr.2018.02.016

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  22 in total

1.  Optimization of transversal relaxation of nitroxides for pulsed electron-electron double resonance spectroscopy in phospholipid membranes.

Authors:  Reza Dastvan; Bela E Bode; Muruga Poopathi Raja Karuppiah; Andriy Marko; Sevdalina Lyubenova; Harald Schwalbe; Thomas F Prisner
Journal:  J Phys Chem B       Date:  2010-10-28       Impact factor: 2.991

2.  Highly efficient, water-soluble polarizing agents for dynamic nuclear polarization at high frequency.

Authors:  Claire Sauvée; Melanie Rosay; Gilles Casano; Fabien Aussenac; Ralph T Weber; Olivier Ouari; Paul Tordo
Journal:  Angew Chem Int Ed Engl       Date:  2013-08-16       Impact factor: 15.336

3.  Successive Stages of Amyloid-β Self-Assembly Characterized by Solid-State Nuclear Magnetic Resonance with Dynamic Nuclear Polarization.

Authors:  Alexey Potapov; Wai-Ming Yau; Rodolfo Ghirlando; Kent R Thurber; Robert Tycko
Journal:  J Am Chem Soc       Date:  2015-06-19       Impact factor: 15.419

4.  Low-temperature dynamic nuclear polarization with helium-cooled samples and nitrogen-driven magic-angle spinning.

Authors:  Kent Thurber; Robert Tycko
Journal:  J Magn Reson       Date:  2016-03       Impact factor: 2.229

5.  Low-temperature dynamic nuclear polarization at 9.4 T with a 30 mW microwave source.

Authors:  Kent R Thurber; Wai-Ming Yau; Robert Tycko
Journal:  J Magn Reson       Date:  2010-03-23       Impact factor: 2.229

6.  Solid state nuclear magnetic resonance with magic-angle spinning and dynamic nuclear polarization below 25 K.

Authors:  Kent R Thurber; Alexey Potapov; Wai-Ming Yau; Robert Tycko
Journal:  J Magn Reson       Date:  2012-11-21       Impact factor: 2.229

7.  Theory for cross effect dynamic nuclear polarization under magic-angle spinning in solid state nuclear magnetic resonance: the importance of level crossings.

Authors:  Kent R Thurber; Robert Tycko
Journal:  J Chem Phys       Date:  2012-08-28       Impact factor: 3.488

8.  Magnetic resonance imaging of organic contrast agents in mice: capturing the whole-body redox landscape.

Authors:  Ryan M Davis; Shingo Matsumoto; Marcelino Bernardo; Anastasia Sowers; Ken-Ichiro Matsumoto; Murali C Krishna; James B Mitchell
Journal:  Free Radic Biol Med       Date:  2010-12-01       Impact factor: 7.376

9.  High-frequency dynamic nuclear polarization using mixtures of TEMPO and trityl radicals.

Authors:  Kan-Nian Hu; Vikram S Bajaj; Melanie Rosay; Robert G Griffin
Journal:  J Chem Phys       Date:  2007-01-28       Impact factor: 3.488

10.  Electron spinal resonance analysis of the nitroxide spin label 2,2,6,6-tetramethylpipidone-N-oxyl (Tempone) in single crystals of the reduced Tempone matrix.

Authors:  W Snipes; J Cupp; G Cohn; A Keith
Journal:  Biophys J       Date:  1974-01       Impact factor: 4.033

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  2 in total

1.  Temperature-Dependent Nuclear Spin Relaxation Due to Paramagnetic Dopants Below 30 K: Relevance to DNP-Enhanced Magnetic Resonance Imaging.

Authors:  Hsueh-Ying Chen; Robert Tycko
Journal:  J Phys Chem B       Date:  2018-10-16       Impact factor: 2.991

2.  Verdazyls as Possible Building Blocks for Multifunctional Molecular Materials: A Case Study on 1,5-Diphenyl-3-(p-iodophenyl)-verdazyl Focusing on Magnetism, Electron Transfer and the Applicability of the Sonogashira-Hagihara Reaction.

Authors:  Hannah Jobelius; Norbert Wagner; Gregor Schnakenburg; Andreas Meyer
Journal:  Molecules       Date:  2018-07-18       Impact factor: 4.411

  2 in total

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