Determining relative proton–proton proximities from the build-up of two-dimensional correlation peaks in 1H double-quantum MAS NMR: insight from multi-spin density-matrix simulations
文献信息
Jonathan P. Bradley, Carmen Tripon, Claudiu Filip, Steven P. Brown
The build-up of intensity—as a function of the number, nrcpl, of POST-C7 elements used for the excitation and reconversion of double-quantum (DQ) coherence (DQC)—is analysed for the fifteen distinct DQ correlation peaks that are observed experimentally for the eight separate 1H resonances in a 1H (500 MHz) DQ CRAMPS solid-state (12.5 kHz MAS) NMR spectrum of the dipeptide β-AspAla (S. P. Brown, A. Lesage, B. Elena, and L. Emsley, J. Am. Chem. Soc., 2004, 126, 13230). The simulation in SPINEVOLUTION (M. Veshtort and R. G. Griffin, J. Magn. Reson., 2006, 178, 248) of t1 (1H DQ evolution) FIDs for clusters of eight dipolar-coupled protons gives separate simulated 1H DQ build-up curves for the CH2(a), CH2(b), CH(Asp), CH(Ala), NH and OH1H single-quantum (SQ) 1H resonances. An analysis of both the simulated and experimental 1H DQ build-up leads to the following general observations: (i) considering the build-up of 1H DQ peaks at a particular SQ frequency, maximum intensity is observed for the DQC corresponding to the shortest H–H distance; (ii) for the maximum intensity 1H DQ peak at a particular SQ frequency, the recoupling time for the observed maximum intensity depends on the corresponding H–H distance, e.g., maximum intensity for the CH2(a)–CH2(b) (H–H distance = 1.55 Å) and OH–CH(Asp) (H–H distance = 2.49 Å) DQ peaks is observed at nrcpl = 2 and 3, respectively; (iii) for DQ peaks involving a CH2proton at a non-CH2 SQ frequency, there is much reduced intensity and a maximum intensity at a short recoupling time; (iv) for the other lower intensity 1H DQ peaks at a particular SQ frequency, maximum intensity is observed for the same (or close to the same) recoupling time, but the relative intensity of the DQ peaks is a reliable indicator of the relative H–H distance—the ratio of the maximum intensities for the peaks at the CH(Ala) SQ frequency due to the two DQCs with the NH and OH protons are found to be approximately in the ratio of the squares of the corresponding dipolar coupling constants. While the simulated 1H DQ build-up curves reproduce most of the features of the experimental curves, maximum intensity is often observed at a longer recoupling time in simulations. In this respect, simulations for two to eight spins show a trend towards a faster decay for an increasing number of considered spins. Finally, simulations show that increasing either the Larmor frequency (to 1 GHz) or the MAS frequency (to 125 kHz) does not lead to changes in the marked differences between the 1H DQ build-up curves at the CH(Asp) SQ frequency for DQCs to the CH2(a) and OH protons that correspond to similar H–H distances (2.39 Å and 2.49 Å, respectively).
相关文献
Single-molecule probing of amyloid nano-ensembles using the polymer nanoarray approach
Sibaprasad Maity, Ekaterina Viazovkina, Alexander Gall, Yuri L. Lyubchenko
DOI: 10.1039/C7CP02691A
The role of non-covalent interactions in the self-healing mechanism of disulfide-based polymers
José M. Asua, Fernando Ruipérez
DOI: 10.1039/C7CP03570E
Multi-spectroscopic and theoretical analyses on the diphenyl ether–tert-butyl alcohol complex in the electronic ground and electronically excited state
Dominic Bernhard, Fabian Dietrich, Mariyam Fatima, Cristobal Perez, Anja Poblotzki, Georg Jansen, Martin A. Suhm, Melanie Schnell, Markus Gerhards
DOI: 10.1039/C7CP02967E
Cation solvation with quantum chemical effects modeled by a size-consistent multi-partitioning quantum mechanics/molecular mechanics method
Maximilian Kubillus, Tomáš Kubař, Robert Stach, Boris Mizaikoff
DOI: 10.1039/C7CP01708A
Highly efficient hydrogen evolution reaction by strain and phase engineering in composites of Pt and MoS2 nano-scrolls
Da Young Hwang, Kyoung Hwan Choi, Jeong Eon Park, Dong Hack Suh
DOI: 10.1039/C7CP03495D
On the mechanism of mechanochemical molecular encapsulation in peptidic capsules
M. P. Szymański, H. Jędrzejewska, M. Wierzbicki, A. Szumna
DOI: 10.1039/C7CP02603J
Predictive models of gas sorption in a metal–organic framework with open-metal sites and small pore sizes
Tony Pham, Katherine A. Forrest, Douglas M. Franz, Zhiyong Guo, Banglin Chen, Brian Space
DOI: 10.1039/C7CP02767B
Observing the real time formation of phosphine-ligated gold clusters by electrospray ionization mass spectrometry
Marshall R. Ligare, Grant E. Johnson, Julia Laskin
DOI: 10.1039/C7CP01402C
On the feasibility of reactions through the fullerene wall: a theoretical study of NHx@C60
Timothy Clark
DOI: 10.1039/C7CP02865B
Probing single-molecule electron–hole transfer dynamics at a molecule–NiO semiconductor nanocrystalline interface
Bharat Dhital, Vishal Govind Rao, H. Peter Lu
DOI: 10.1039/C7CP01476G
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。
来源期刊
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.













![2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure 2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure](https://cnstatic.chemtradehub.com/structs/253/25332-39-2-496e.webp)
![3-[(4-Nitrobenzyl)oxy]-3-oxopropanoic Acid structure 3-[(4-Nitrobenzyl)oxy]-3-oxopropanoic Acid structure](https://cnstatic.chemtradehub.com/structs/773/77359-11-6-0d04.webp)