Pulsed Dynamic Nuclear Polarization

被引:26
作者
Tan, Kong Ooi [1 ]
Jawla, Sudheer [2 ]
Temkin, Richard J. [2 ]
Griffin, Robert G. [1 ]
机构
[1] MIT, Dept Chem, Francis Bitter Magnet Lab, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Plasma Sci & Fus Ctr, 77 Massachusetts Ave, Cambridge, MA 02139 USA
来源
EMAGRES | 2019年 / 8卷 / 03期
基金
瑞士国家科学基金会;
关键词
hyperpolarization; dynamic nuclear polarization; pulsed DNP; MAS-DNP; solid-state NMR; FREQUENCY-MODULATION; STATE NMR; DNP; RESONANCE; SPECTROMETER; SPECTROSCOPY; ORIENTATION; ENDOR; SPINS; EPR;
D O I
10.1002/9780470034590.emrstm1551
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
In the last two decades continuous-wave (CW) microwave irradiation obtained from gyrotron microwave sources has been utilized extensively in the development and applications of new experimental approaches to high frequency dynamic nuclear polarization (DNP). Despite the abundant successes of this approach, it is well established experimentally and understood theoretically that at higher magnetic fields, where the resolution of the NMR spectra is optimal, the enhancement factors in CW DNP experiments decrease. Potentially this issue can be mitigated by using time domain or pulsed DNP techniques, which theoretically have field-independent enhancement factors. In this contribution, we discuss the pulsed DNP experiments that have been developed to date, along with the theory and the applicability of the sequences. As we will see pulsed techniques are fundamentally different from the CW-DNP methodology and require a different array of instrumentation, spin physics, and radicals. Hence, in addition to the underlying theory, we discuss the specifications of the microwave sources, DNP probes, and optimal radicals for pulsed DNP. The review ends with a summary of the current and future applications of pulsed DNP and conjectures as to the development of the pulsed methods for experiments at increasingly higher magnetic fields.
引用
收藏
页码:339 / 351
页数:13
相关论文
共 72 条
[1]  
ABRAGAM A, 1958, CR HEBD ACAD SCI, V246, P2253
[2]   PRINCIPLES OF DYNAMIC NUCLEAR-POLARIZATION [J].
ABRAGAM, A ;
GOLDMAN, M .
REPORTS ON PROGRESS IN PHYSICS, 1978, 41 (03) :395-467
[3]   NUCLEAR MAGNETIC RESONANCE SPECTRA FROM A CRYSTAL ROTATED AT HIGH SPEED [J].
ANDREW, ER ;
BRADBURY, A ;
EADES, RG .
NATURE, 1958, 182 (4650) :1659-1659
[4]  
Baldus M, 1998, MOL PHYS, V95, P1197, DOI 10.1080/00268979809483251
[5]   CHEMICAL-SHIFT CORRELATION SPECTROSCOPY IN ROTATING SOLIDS - RADIO FREQUENCY-DRIVEN DIPOLAR RECOUPLING AND LONGITUDINAL EXCHANGE [J].
BENNETT, AE ;
OK, JH ;
GRIFFIN, RG ;
VEGA, S .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (11) :8624-8627
[6]   SPIN-TEMPERATURE MODEL OF NUCLEAR DYNAMIC POLARIZATION USING FREE RADICALS [J].
BORGHINI, M .
PHYSICAL REVIEW LETTERS, 1968, 20 (09) :419-&
[7]   Microwave frequency modulation to enhance Dissolution Dynamic Nuclear Polarization [J].
Bornet, Aurelien ;
Milani, Jonas ;
Vuichoud, Basile ;
Linde, Angel J. Perez ;
Bodenhausen, Geoffrey ;
Jannin, Sami .
CHEMICAL PHYSICS LETTERS, 2014, 602 :63-67
[8]   Frequency-Swept Integrated and Stretched Solid Effect Dynamic Nuclear Polarization [J].
Can, T. V. ;
McKay, J. E. ;
Weber, R. T. ;
Yang, C. ;
Dubroca, T. ;
van Tol, J. ;
Hill, S. ;
Griffin, R. G. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2018, 9 (12) :3187-3192
[9]   Ramped- amplitude NOVEL [J].
Can, T. V. ;
Weber, R. T. ;
Walish, J. J. ;
Swager, T. M. ;
Griffin, R. G. .
JOURNAL OF CHEMICAL PHYSICS, 2017, 146 (15)
[10]   Time domain DNP with the NOVEL sequence [J].
Can, T. V. ;
Walish, J. J. ;
Swager, T. M. ;
Griffin, R. G. .
JOURNAL OF CHEMICAL PHYSICS, 2015, 143 (05)