Simultaneous DNP enhancements of 1H and 13C nuclei: theory and experiments
Literature Information
Daphna Shimon, Yonatan Hovav, Ilia Kaminker, Akiva Feintuch, Daniella Goldfarb, Shimon Vega
DNP on heteronuclear spin systems often results in interesting phenomena such as the polarization enhancement of one nucleus during MW irradiation at the “forbidden” transition frequencies of another nucleus or the polarization transfer between the nuclei without MW irradiation. In this work we discuss the spin dynamics in a four-spin model system of the form {ea–eb–(1H,13C)}, with the Larmor frequencies ωa, ωb, ωH and ωC, by performing Liouville space simulations. This spin system exhibits the common 1H solid effect (SE), 13C cross effect (CE) and in addition high order CE-DNP enhancements. Here we show, in particular, the “proton shifted 13C-CE” mechanism that results in 13C polarization when the model system, at one of its 13C-CE conditions, is excited by a MW field at the zero quantum or double quantum electron–proton transitions ωMW = ωa ± ωH and ωMW = ωb ± ωH. Furthermore, we introduce the “heteronuclear” CE mechanism that becomes efficient when the system is at one of its combined CE conditions |ωa − ωb| = |ωH ± ωC|. At these conditions, simulations of the four-spin system show polarization transfer processes between the nuclei, during and without MW irradiation, resembling the polarization exchange effects often discussed in the literature. To link the “microscopic” four-spin simulations to the experimental results we use DNP lineshape simulations based on “macroscopic” rate equations describing the electron and nuclear polarization dynamics in large spin systems. This approach is applied based on electron–electron double resonance (ELDOR) measurements that show strong 1H-SE features outside the EPR frequency range. Simulated ELDOR spectra combined with the indirect 13C-CE (iCE) mechanism, result in additional “proton shifted 13C-CE” features that are similar to the experimental ones. These features are also observed experimentally in 13C-DNP spectra of a sample containing 15 mM of trityl in a glass forming solution of 13C-glycerol/H2O and are analyzed by calculating the basic 13C-SE and 13C-iCE shapes using simulated ELDOR spectra that were fitted to the experimental ones.
Recommended Journals
Related Literature
Hydrogen evolution in [NiFe] hydrogenases and related biomimetic systems: similarities and differences
Ranjita Das, Frank Neese, Maurice van Gastel
DOI: 10.1039/C6CP03672D
Insight into the pseudo π-hole interactions in the M3H6⋯(NCF)n (M = C, Si, Ge, Sn, Pb; n = 1, 2, 3) complexes
Yanli Zeng, Xiaoyan Li, Zheng Sun, Lingpeng Meng
DOI: 10.1039/C6CP03713E
A strategy to achieve enhanced electromagnetic interference shielding at low concentration with a new generation of conductive carbon black in a chlorinated polyethylene elastomeric matrix
Subhadip Mondal, Sayan Ganguly, Mostafizur Rahaman, Ali Aldalbahi, Tapan K. Chaki, Dipak Khastgir, Narayan Ch. Das
DOI: 10.1039/C6CP04274K
Structural characteristics of hydrated protons in the conductive channels: effects of confinement and fluorination studied by molecular dynamics simulation
Ning Zhang, Yuechun Song, Xuehua Ruan, Xiaoming Yan, Zhao Liu, Zhuanglin Shen, Xuemei Wu
DOI: 10.1039/C6CP03012B
Hydrated forms of fluoroacetic acid: a rotational study
Luca Evangelisti, Lorenzo Spada, Susana Blanco, Walther Caminati
DOI: 10.1039/C6CP04735A
Rotational dynamics of water molecules near biological surfaces with implications for nuclear quadrupole relaxation
Daniel Braun, Michael Schmollngruber, Othmar Steinhauser
DOI: 10.1039/C6CP04000D
ZnO nanorods prepared via ablation of Zn with millisecond laser in liquid media
Taku Goto, Tatsuki Owashi, Alex G. Rozhin, Shigeru Yamaguchi, Tsuyohito Ito
DOI: 10.1039/C6CP04556A
Factors controlling the CO intercalation of h-BN overlayers on Ru(0001)
Aiyi Dong, Qiang Fu, Hao Wu, Mingming Wei, Xinhe Bao
DOI: 10.1039/C6CP03660K
Prediction of two-photon absorption enhancement in red fluorescent protein chromophores made from non-canonical amino acids
M. Alaraby Salem, Isaac Twelves, Alex Brown
DOI: 10.1039/C6CP03865D
You might also like
Is 2-(2-chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) safe?
2-(2-Chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) is generally consi...
Is 2-(Benzyloxy)-5-bromobenzoic acid (CAS: 62176-31-2) safe?
2-(Benzyloxy)-5-bromobenzoic acid can be handled safely if appropriate precautio...
What is (4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride (CAS: 1159825-48-5)?
(4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride is a chemical compound ...
What is 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54-7)?
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54...
Are there alternatives to 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS: 102771-26-6) in synthesis?
While 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS:...
What is the market or research trend for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine-6-carboxylate (CAS: 851376-80-2)?
The market for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine...
How should waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) be handled?
Waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) should ...
How is (6-Fluoro-3-pyridinyl)boronic acid (CAS: 351019-18-6) typically synthesized?
(6-Fluoro-3-pyridinyl)boronic acid can be synthesized through the reaction of 6-...
What industries use Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9)?
Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9) finds applications in vario...
What is the market or research trend for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4)?
The market for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4) is g...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.










![19-[Chloro(dideuterio)methyl]-19-deuterio-20,20-dideuteriooxyoctatriacontane-18,21-dione structure 19-[Chloro(dideuterio)methyl]-19-deuterio-20,20-dideuteriooxyoctatriacontane-18,21-dione structure](https://static.chemtradehub.com/structs/124/1246818-85-8-6244.webp)



